Tender For Rate Contract For Supply Of Consumables/Non-Consumables For The Department Of Cardiology
Tender Overview
Project Description
Rate Contract For Supply Of Consumables / Non-Consumables For The Department Of Cardiology , Important Conditions For Cardiology Tender: Abbreviations And Additional Conditions 1. S-Items With ( Prefix S ) Sample Must Be Submitted To The Department With Item Number And Name Superscribed Within 15 Days Of Online Tender Opening, 2. Ex-Patient Size Variable Implantable Devices And Consumables ( Prefix Ex ) ( Stents / Asd / Vsd / Pda / Balloons / Coils / Etc- The Supplier Should Maintain A Stock Of All The Sizes In The Matrix In The Cath Labs So As To Exchange The Items Suitable For An Individual Patient Till The Last Item Is Used. 3. D- Items Which Has A Prefix ( D ) Has To Be Demonstrated By The Vendor To The Departmental Selection Committee On The Date Of Technical Evaluation Informed By Email Only 4. All Implantable Devices Should Be Licensed For Sale In India By Dcgi / Cdsco And Should Be Usfda Approved, Failing Which Human Clinical Trial Rct Data Published In Indexed Journals Should Be Submitted 5. All Implantable Devices Should Be Supplied Only By Companies That Have Supplied To Major Hospitals ( 500 Beds ) In India Or Abroad ( Proof To Be Enclosed ) 6. Items Supplied Should Have An Expiration Date Of More Than 12 Months From The Date Of Supply. 7. For Some Items Like Bmv Ballons And Asd / Vsd / Pda Devices, Cables And Accessories Shall Be Bought From The Same Company Selected As L1 In The Category Of Device Only Item8. For All Items, A Detailed Technical Brochure In Pdf Format And Approvals, Certifications, Etc Have To Be Sent To The Department Stores Within 10 Days Of Online Tender Opening To [email protected] With The Subject As The Tenderno / Serial No / Item Name / Manufacturer Name / Brand Name 9. While Mentioning The Make / Model Of Consumable / Implant / Non-Consumable, Please Mention The Manufacturer Name And Model Name Model Number 10.Non-Compliance Of All The Above Clauses Will Lead To The Rejection Of The Item1. Femoral Access , ( S ) Femoralsheath Systems Size 4F 7.5 Cm With Accessories For Insertion.Should Be Fda / Ce / Dcgi Approved , ( S ) Femoralsheath Systems Size 4F 11 Cm With Accessories For Insertion.Should Be Fda / Ce / Dcgi Approved , ( S ) Femoral Sheath Systems Sizes 5F 7.5 Cm With Accessories For Insertion.Should Be Fda / Ce / Dcgi Approved , ( S ) Femoral Sheath Systems Sizes 5F 11 Cm With Accessories For Insertion.Should Be Fda / Ce / Dcgi Approved , ( S ) Femoral Sheath Systems Sizes 6F 7.5 Cm With Accessories For Insertion.Should Be Fda / Ce / Dcgi Approved , ( S ) Femoral Sheath Systems Sizes 6F 11 Cm With Accessories For Insertion.Should Be Fda / Ce / Dcgi Approved , ( S ) Femoral Sheath Systems Sizes 7F 7.5 Cm With Accessories For Insertion.Should Be Fda / Ce / Dcgi Approved , ( S ) Femoral Sheath Systems Sizes 7F 11 Cm With Accessories For Insertion.Should Be Fda / Ce / Dcgi Approved , ( S ) Femoral Sheath Systems Sizes 8F 7.5 Cm With Accessories For Insertion.Should Be Fda / Ce / Dcgi Approved , ( S ) Femoral Sheath Systems Sizes 8F 11 Cm With Accessories For Insertion.Should Be Fda / Ce / Dcgi Approved , ( S ) Femoral Sheath Systems Sizes 9F 7.5 Cm With Accessories For Insertion.Should Be Fda / Ce / Dcgi Approved , ( S ) Femoral Sheath Systems Sizes 9F 11 Cm With Accessories For Insertion.Should Be Fda / Ce / Dcgi Approved , ( S ) Femoral Sheath Systems Sizes 10F 7.5 Cm With Accessories For Insertion.Should Be Fda / Ce / Dcgi Approved , ( S ) Femoral Sheath Systems Sizes 10F 11 Cm With Accessories For Insertion.Should Be Fda / Ce / Dcgi Approved , ( S ) Femoral Sheath Systems Sizes 11F 7.5 Cm With Accessories For Insertion.Should Be Fda / Ce / Dcgi Approved , ( S ) Femoral Sheath Systems Sizes 11F 11 Cm With Accessories For Insertion.Should Be Fda / Ce / Dcgi Approved , ( S ) Femoral Sheath Systems Sizes 12F 7.5 Cm With Accessories For Insertion.Should Be Fda / Ce / Dcgi Approved , ( S ) Femoral Sheath Systems Sizes 12F 11 Cm With Accessories For Insertion.Should Be Fda / Ce / Dcgi Approved , ( S ) Femoral Sheath Systems Sizes 14F 7.5 Cm With Accessories For Insertion.Should Be Fda / Ce / Dcgi Approved , ( S ) Femoral Sheath Systems Sizes 14F 11 Cm With Accessories For Insertion.Should Be Fda / Ce / Dcgi Approved , ( S ) Femoral Sheath Systems Sizes 5F 23 Cm With Accessories For Insertion.Should Be Fda / Ce / Dcgi Approved , ( S ) Femoral Sheath Systems Sizes 6F 23 Cm With Accessories For Insertion.Should Be Fda / Ce / Dcgi Approved , ( S ) Femoral Sheath Systems Sizes 7F 23 Cm With Accessories For Insertion.Should Be Fda / Ce / Dcgi Approved , ( S ) Femoral Sheath Systems Sizes 8F 23 Cm With Accessories For Insertion.Should Be Fda / Ce / Dcgi Approved , Radial Access , ( S ) Transradial Sheath Systems With Hydrophilic Coating On The Sheath, Tapering Hydrophilic Dilator, Hydrophilic Straight Polymer 018 Wires And 20G Plastic Cannula For Puncture 4F 7Cm.Should Be Fda / Ce / Dcgi Approved , ( S ) Transradial Sheath Systems With Hydrophilic Coating On The Sheath, Tapering Hydrophilic Dilator, Hydrophilic Straight Polymer 021 Wires And 20G Plastic Cannula For Puncture 4F 7Cm.Should Be Fda / Ce / Dcgi Approved , ( S ) Transradial Sheath Systems With Hydrophilic Coating On The Sheath, Tapering Hydrophilic Dilator, Hydrophilic Straight Polymer 025 Wires And 20G Plastic Cannula For Puncture 4F 7Cm.Should Be Fda / Ce / Dcgi Approved , ( S ) Transradial Sheath Systems With Hydrophilic Coating On The Sheath, Tapering Hydrophilicdilator Hydrophilic Straight Polymer 018 Wires And 20G Plastic Cannula For Puncture 4F 11Cm.Should Be Fda / Ce / Dcgi Approved , ( S ) Transradial Sheath Systems With Hydrophilic Coating On The Sheath, Tapering Hydrophilicdilator Hydrophilic Straight Polymer 021 Wires And 20G Plastic Cannula For Puncture 4F 11Cm.Should Be Fda / Ce / Dcgi Approved , ( S ) Transradial Sheath Systems With Hydrophilic Coating On The Sheath, Tapering Hydrophilicdilator Hydrophilic Straight Polymer 025 Wires And 20G Plastic Cannula For Puncture 4F 11Cm.Should Be Fda / Ce / Dcgi Approved , ( S ) Transradial Sheath Systems With Hydrophilic Coating On Sheath, Tapering Dilator Hydrophilic Staright Polymer 018 Wires And 20G Plastic Cannula For Puncture 5F 7Cm.Should Be Fda / Ce / Dcgi Approved , ( S ) Transradial Sheath Systems With Hydrophilic Coating On Sheath, Tapering Dilator Hydrophilic Staright Polymer 021 Wires And 20G Plastic Cannula For Puncture 5F 7Cm.Should Be Fda / Ce / Dcgi Approved , ( S ) Transradial Sheath Systems With Hydrophilic Coating On Sheath, Tapering Dilator Hydrophilic Staright Polymer 025 Wires And 20G Plastic Cannula For Puncture 5F 7Cm.Should Be Fda / Ce / Dcgi Approved , ( S ) Transradial Sheath Systems With Hydrophilic Coating On Sheath, Tapering Dilator Hydrophilic Staright Polymer 018 Wires And 20G Plastic Cannula For Puncture 5F 11Cm.Should Be Fda / Ce / Dcgi Approved , ( S ) Transradial Sheath Systems With Hydrophilic Coating On Sheath, Tapering Dilator Hydrophilic Staright Polymer 021 Wires And 20G Plastic Cannula For Puncture 5F 11Cm.Should Be Fda / Ce / Dcgi Approved , ( S ) Transradial Sheath Systems With Hydrophilic Coating On Sheath, Tapering Dilator Hydrophilic Staright Polymer 025 Wires And 20G Plastic Cannula For Puncture 5F 11Cm.Should Be Fda / Ce / Dcgi Approved , ( S ) Transradial Sheath Systems With Hydrophilic Coating On Sheath, Tapering Dilator Hydrophilic Staright Polymer 018 Wires And 20G Plastic Cannula For Puncture6f 7Cm.Should Be Fda / Ce / Dcgi Approved , ( S ) Transradial Sheath Systems With Hydrophilic Coating On Sheath, Tapering Dilator Hydrophilic Staright Polymer 021 Wires And 20G Plastic Cannula For Puncture6f 7Cm.Should Be Fda / Ce / Dcgi Approved , ( S ) Transradial Sheath Systems With Hydrophilic Coating On Sheath, Tapering Dilator Hydrophilic Staright Polymer 025 Wires And 20G Plastic Cannula For Puncture6f 7Cm.Should Be Fda / Ce / Dcgi Approved , ( S ) Transradial Sheath Systems With Hydrophilic Coating On Sheath, Tapering Dilator Hydrophilic Staright Polymer 018 Wires And 20G Plastic Cannula For Puncture6f 11Cm.Should Be Fda / Ce / Dcgi Approved , ( S ) Transradial Sheath Systems With Hydrophilic Coating On Sheath, Tapering Dilator Hydrophilic Staright Polymer 021 Wires And 20G Plastic Cannula For Puncture6f 11Cm.Should Be Fda / Ce / Dcgi Approved , ( S ) Transradial Sheath Systems With Hydrophilic Coating On Sheath, Tapering Dilator Hydrophilic Staright Polymer 025 Wires And 20G Plastic Cannula For Puncture6f 11Cm.Should Be Fda / Ce / Dcgi Approved , ( S ) Transradial Sheath Systems With Hydrophilic Coating On Sheath, Tapering Dilator Hydrophilic Staright Polymer 018 Wires And 20G Plastic Cannula For Puncture 7F 7Cm.Should Be Fda / Ce / Dcgi Approved , ( S ) Transradial Sheath Systems With Hydrophilic Coating On Sheath, Tapering Dilator Hydrophilic Staright Polymer 021 Wires And 20G Plastic Cannula For Puncture 7F 7Cm.Should Be Fda / Ce / Dcgi Approved , ( S ) Transradial Sheath Systems With Hydrophilic Coating On Sheath, Tapering Dilator Hydrophilic Staright Polymer 025 Wires And 20G Plastic Cannula For Puncture 7F 7Cm.Should Be Fda / Ce / Dcgi Approved , ( S ) Transradial Sheath Systems With Hydrophilic Coating On Sheath, Tapering Dilator Hydrophilic Staright Polymer 018 Wires And 20G Plastic Cannula For Puncture 7F 11Cm.Should Be Fda / Ce / Dcgi Approved , ( S ) Transradial Sheath Systems With Hydrophilic Coating On Sheath, Tapering Dilator Hydrophilic Staright Polymer 021 Wires And 20G Plastic Cannula For Puncture 7F 11Cm.Should Be Fda / Ce / Dcgi Approved , ( S ) Transradial Sheath Systems With Hydrophilic Coating On Sheath, Tapering Dilator Hydrophilic Staright Polymer 025 Wires And 20G Plastic Cannula For Puncture 7F 11Cm.Should Be Fda / Ce / Dcgi Approved , ( S ) Transradial Slender Sheath Systems 5F 10 Cm Capable Of Introducing 6F Catheter With Hydrophilic Coating On Sheath, Tapering Dilator Hydrophilic Staright Polymer 021 Wires And 20G Plastic Cannula For Puncture .Should Be Fda / Ce / Dcgi Approved , ( S ) Transradial Slender Sheath Systems 5F 10 Cm Capable Of Introducing 6F Catheter With Hydrophilic Coating On Sheath, Tapering Dilator Hydrophilic Staright Polymer 025 Wires And 20G Plastic Cannula For Puncture .Should Be Fda / Ce / Dcgi Approved , ( S ) Transradial Slender Sheath Systems 5F 16 Cm Capable Of Introducing 6F Catheter With Hydrophilic Coating On Sheath, Tapering Dilator Hydrophilic Staright Polymer 021 Wires And 20G Plastic Cannula For Puncture .Should Be Fda / Ce / Dcgi Approved , ( S ) Transradial Slendersheath Systems 6F 10 Cm Capable Of Introducing 7F Catheter With Hydrophilic Coating On Sheath, Tapering Dilator Hydrophilic Staright Polymer 021 Wires And 20G Plastic Cannula For Puncture .Should Be Fda / Ce / Dcgi Approved , ( S ) Transradial Slendersheath Systems 6F 10 Cm Capable Of Introducing 7F Catheter With Hydrophilic Coating On Sheath, Tapering Dilator Hydrophilic Staright Polymer 025 Wires And 20G Plastic Cannula For Puncture .Should Be Fda / Ce / Dcgi Approved , ( S ) Transradial Slendersheath Systems 6F16 Cm Capable Of Introducing 7F Catheter With Hydrophilic Coating On Sheath, Tapering Dilator Hydrophilic Staright Polymer 021 Wires And 20G Plastic Cannula For Puncture .Should Be Fda / Ce / Dcgi Approved , ( S ) Transradial Slendersheath Systems 7F 10 Cm Capable Of Introducing 8F Catheter With Hydrophilic Coating On Sheath, Tapering Dilator Hydrophilic Staright Polymer 021 Wires And 20G Plastic Cannula For Puncture .Should Be Fda / Ce / Dcgi Approved , ( S ) Transradial Slendersheath Systems 7F 10 Cm Capable Of Introducing 7F Catheter With Hydrophilic Coating On Sheath, Tapering Dilator Hydrophilic Staright Polymer 025 Wires And 20G Plastic Cannula For Puncture .Should Be Fda / Ce / Dcgi Approved , ( S ) Transradial Slendersheath Systems 7F16 Cm Capable Of Introducing 8F Catheter With Hydrophilic Coating On Sheath, Tapering Dilator Hydrophilic Staright Polymer 021 Wires And 20G Plastic Cannula For Puncture .Should Be Fda / Ce / Dcgi Approved , Access Closure , ( S ) Femoral Vascular Closure Device Collagen Based Femoral 6F Should Be Fda / Ce / Dcgi Approved , ( S ) Femoral Vascular Closure Device Collagen Based Femoral8f Should Be Fda / Ce / Dcgi Approved , ( S ) Femoral Vascular Closure Device Prolene Sutured Capable Of Closing Upto 21F Devices.Should Be Fda Or Ce Anddcgi Approved , ( S ) Collagen Anchor Based Femoral Vascular Closure Device Capable Of Closing Large Bore Access Ranging From 12 To 25 Fr.Should Be Fda / Ce / Dcgi Approved , ( S ) Radial Compression Device Balloon Inflation Type Transparent .Should Be Fda / Ce / Dcgi Approved , ( S ) Radial Compression Device Screw Type .Should Be Fda / Ce / Dcgi Approved , ( S ) Polymer Reinforced Adhesive Skin Closure Strips 6Mm X 100Mm , ( S ) Semipermeable Waterproof Plastic Wound Dressing With Pad ( Dressing Size Of 9 X 15Cm And Pad Size 5 X 10Cm ) , Diagnostic Catheters , ( S ) Cournand Catheter 5F, 6F 110 Cm Woven Dacron.Should Be Fda / Ce / Dcgi Approved , ( S ) Goodale-Lubin Catheter 6F, 7F 100 / 125 Cm Woven Dacron.Should Be Fda / Ce / Dcgi Approved , ( S ) Judkins Left Catheter 4F 90 / 110 Cm All Curves.Should Be Fda / Ce / Dcgi Approved , ( S ) Judkins Left Catheter 5F, 6F 110 Cm All Curves.Should Be Fda / Ce / Dcgi Approved , ( S ) Judkins Right Catheter 4F, 90 / 110Cm All Curves.Should Be Fda / Ce / Dcgi Approved , ( S ) Judkins Right Catheter 5F, 6F 110Cm All Curves.Should Be Fda / Ce / Dcgi Approved , ( S ) Amplatz Left Catheter 4F 90 / 110Cmall Curves.Should Be Fda / Ce / Dcgi Approved , ( S ) Amplatz Left Catheter5f, 6F 110Cm All Curves.Should Be Fda / Ce / Dcgi Approved , ( S ) Amplatz Right Catheter 4F 90 / 110 Cmall Curves.Should Be Fda / Ce / Dcgi Approved , ( S ) Amplatz Right Catheter 5F, 6F 110Cm All Curves.Should Be Fda / Ce / Dcgi Approved , ( S ) Left Coronary By Pass Catheter 4F, 5F, 6F 110Cm All Curves.Should Be Fda / Ce / Dcgi Approved , ( S ) Right Coronary By Pass Catheter 4F, 5F, 6F 110Cm All Curves.Should Be Fda / Ce / Dcgi Approved , ( S ) Internal Mammary Artery Catheter 4F, 5F, 6F 110Cm All Curves.Should Be Fda / Ce / Dcgi Approved , ( S ) Multipurpose Catheter 4F 90 / 110Cm A1, A2, B1, B2.Should Be Fda / Ce / Dcgi Approved , ( S ) Multipurpose Catheter 5F110cm A1, A2, B1, B2. Should Be Fda / Ce / Dcgi Approved , ( S ) Multipurpose Catheter 6F 110Cm A1, A2, B1, B2.Should Be Fda / Ce / Dcgi Approved , ( S ) Radial Cag Tig Catheters With Hydrophilic Coating Single Side-Hole 5F 100Cmsmall Curves.Should Be Fda / Ce / Dcgi Approved , ( S ) Radial Cag Tig Catheters With Hydrophilic Coating Single Side-Hole5f 110Cmsmall Curves.Should Be Fda / Ce / Dcgi Approved , ( S ) Radial Cag Tig Catheterswith Hydrophilic Coating Single Side-Hole 5F 100Cmintermediate Curves.Should Be Fda / Ce / Dcgi Approved , ( S ) Radial Cag Tig Catheters With Hydrophilic Coating Single Side-Hole5f 110Cmintermediate Curves.Should Be Fda / Ce / Dcgi Approved , ( S ) Radial Cag Tig Catheterswith Hydrophilic Coating Single Side-Hole 5F 100Cmlarge Curves.Should Be Fda / Ce / Dcgi Approved , ( S ) Radial Cag Tig Catheters With Hydrophilic Coating Single Side-Hole5f 110Cmlarge Curves.Should Be Fda / Ce / Dcgi Approved , ( S ) Radial Cag Tig Catheters With Hydrophilic Coating Single Side-Hole5f 100Cmextralarge Curves.Should Be Fda / Ce / Dcgi Approved , ( S ) Radial Cag Tig Catheterswith Hydrophilic Coating Single Side-Hole 5F 110Cmextralarge Curves.Should Be Fda / Ce / Dcgi Approved , ( S ) Radial Cag Tig Catheters With Hydrophilic Coating Two Side-Hole 5F 100Cmsmall Curves.Should Be Fda / Ce / Dcgi Approved , ( S ) Radial Cag Tig Catheters With Hydrophilic Coating Two Side-Hole5f 110Cmsmall Curves.Should Be Fda / Ce / Dcgi Approved , ( S ) Radial Cag Tig Catheterswith Hydrophilic Coating Two Side-Hole 5F 100Cmintermediate Curves.Should Be Fda / Ce / Dcgi Approved , ( S ) Radial Cag Tig Catheters With Hydrophilic Coating Two Side-Hole5f 110Cmintermediate Curves.Should Be Fda / Ce / Dcgi Approved , ( S ) Radial Cag Tig Catheterswith Hydrophilic Coating Two Side-Hole 5F 100Cmlarge Curves.Should Be Fda / Ce / Dcgi Approved , ( S ) Radial Cag Tig Catheters With Hydrophilic Coating Two Side-Hole5f 110Cmlarge Curves.Should Be Fda / Ce / Dcgi Approved , ( S ) Radial Cag Tig Catheters With Hydrophilic Coating Two Side-Hole5f 100Cmextralarge Curves.Should Be Fda / Ce / Dcgi Approved , ( S ) Radial Cag Tig Catheterswith Hydrophilic Coating Two Side-Hole 5F 110Cmextralarge Curves.Should Be Fda / Ce / Dcgi Approved , ( S ) Pig Tail Catheters4f 90Cm.Should Be Fda / Ce / Dcgi Approved , ( S ) Pig Tail Catheters4f 110Cm.Should Be Fda / Ce / Dcgi Approved , ( S ) Pig Tail Catheters4f 150Cm.Should Be Fda / Ce / Dcgi Approved , ( S ) Pig Tail Catheters 5F 90Cm.Should Be Fda / Ce / Dcgi Approved , ( S ) Pig Tail Catheters5f 110Cm.Should Be Fda / Ce / Dcgi Approved , ( S ) Pig Tail Catheters5f 150Cm.Should Be Fda / Ce / Dcgi Approved , ( S ) Pig Tail Catheters6f 90Cm.Should Be Fda / Ce / Dcgi Approved , ( S ) Pig Tail Catheters6f 110Cm.Should Be Fda / Ce / Dcgi Approved , ( S ) Pig Tail Catheters6f 150Cm.Should Be Fda / Ce / Dcgi Approved , ( S ) Angled Pig Tail Catheters4f 90Cm.Should Be Fda / Ce / Dcgi Approved , ( S ) Angled Pig Tail Catheters4f 110Cm.Should Be Fda / Ce / Dcgi Approved , ( S ) Angled Pig Tail Catheters4f 150Cm.Should Be Fda / Ce / Dcgi Approved , ( S ) Angled Pig Tail Catheters5f 90Cm.Should Be Fda / Ce / Dcgi Approved , ( S ) Angled Pig Tail Catheters5f 110Cm.Should Be Fda / Ce / Dcgi Approved , ( S ) Angled Pig Tail Catheters5f 150Cm.Should Be Fda / Ce / Dcgi Approved , ( S ) Angled Pig Tail Catheters6f 90Cm.Should Be Fda / Ce / Dcgi Approved , ( S ) Angled Pig Tail Catheters6f 110Cm.Should Be Fda / Ce / Dcgi Approved , ( S ) Angled Pig Tail Catheters6f 150Cm.Should Be Fda / Ce / Dcgi Approved , ( S ) Markerpigtail Catheter 4F 90Cm. Should Be Fda / Ce / Dcgi Approved , ( S ) Markerpigtail Catheter 4F 110Cm .Should Be Fda / Ce / Dcgi Approved , ( S ) Markerpigtail Catheter 4F 150Cm .Should Be Fda / Ce / Dcgi Approved , ( S ) Markerpigtail Catheter 5F 90Cm .Should Be Fda / Ce / Dcgi Approved , ( S ) Markerpigtail Catheter 5F 110Cm .Should Be Fda / Ce / Dcgi Approved , ( S ) Markerpigtail Catheter 5F 150Cm .Should Be Fda / Ce / Dcgi Approved , ( S ) Markerpigtail Catheter 6F 90Cm .Should Be Fda / Ce / Dcgi Approved , ( S ) Markerpigtail Catheter 6F 110Cm .Should Be Fda / Ce / Dcgi Approved , ( S ) Markerpigtail Catheter 6F 150Cm .Should Be Fda / Ce / Dcgi Approved , Nih Angiography Catheter 4Fshould Be Fda / Ce / Dcgi Approved , Nih Angiography Catheter 5F / 6F Should Be Fda / Ce / Dcgi Approved , Berman Angiography Catheter 4F 60 / 90 / 110 Cm Should Be Fda / Ce / Dcgi Approved , Berman Angiography Catheter 5F And 6F60 / 90 / 110 Cm Should Be Fda / Ce / Dcgi Approved , Reverse Berman Angiography Catheter 4F 60 / 90 / 110 Cm Should Be Fda / Ce / Dcgi Approved , Reverse Berman Angiography Catheter 4F 60 / 90 / 110 Cm Should Be Fda / Ce / Dcgi Approved , Multitrack Angiography Cathetercapable Of Doing Angiography With Guidewire Insitu4f 80 / 100Cmshould Be Fda / Ce / Dcgi Approved , Multitrack Angiography Catheter Capable Of Doing Angiography With Guidewire Insitu 5F 80 / 100Cm Should Be Fda / Ce / Dcgi Approved , Multitrack Angiography Catheter Capable Of Doing Angiography With Guidewire Insitu 6F 80 / 100Cm Should Be Fda / Ce / Dcgi Approved , Accessories , ( S ) Initial Puncture Needles18g Should Be Fda / Ce / Dcgi Approved , ( S ) Micropuncture Neonatal Introducer Sets And Sheath Systems 4F Should Be Fda / Ce / Dcgi Approved , ( S ) Micropuncture Neonatal Introducer Sets And Sheath Systems 5F.Should Be Fda / Ce / Dcgi Approved , ( S ) Micropuncture Introducer Set Suitable For Ultrasound Guided Vascular Access.Should Include One 21G 7Cm Micropuncture Needle, One 0.18 Guide Wire And One 5F Introducer Sheath As One Set , ( S ) 3 / 3 Rotating Manifold For Cag.Should Be Fda / Ce / Dcgi Approved , ( S ) 3 / 3 Rotating Manifold For Ptca.Should Be Fda / Ce / Dcgi Approved , ( S ) Touhey Borst Y Connector- Push Pull Type And Introducer Needle For Ptca.Should Be Fda / Ce / Dcgi Approved , ( S ) Touhey Borst Y Connector- Screw Type And Introducer Needle For Ptca.Should Be Fda / Ce / Dcgi Approved , ( S ) Y Connector 10F Diameter Having A Larger Inner Lumen For Peripheral Interventions.Should Be Fda / Ce / Dcgi Approved , ( S ) Torquer Device For 014 Guide Wire , ( S ) Torquer Device For 018 Guide Wire , ( S ) Torquer Device For 021 Guide Wire , ( S ) Torquer Device For 025 Guide Wire , ( S ) Torquer Device For 035 Guide Wire , ( S ) Torquer Device For 038 Guide Wire , ( S ) Pressure Manometer Lines Male / Female 150 Cm.Should Be Fda / Ce / Dcgi Approved , ( S ) Pressure Manometer Lines Male / Male 150 Cm.Should Be Fda / Ce / Dcgi Approved , ( S ) Three Way Stopcocks.Should Be Fda / Ce / Dcgi Approved , ( S ) High Pressure Contrast Injection Tube.Should Be Fda / Ce / Dcgi Approved , ( S ) High Flow Angio Flush Caths.Should Be Fda / Ce / Dcgi Approved , ( S ) 3 Ring Control Syringes 20Cc.Should Be Fda / Ce / Dcgi Approved , ( S ) 3 Ring Control Syringes Transparent With Markers 20Cc.Should Be Dcgi Approved , ( S ) Femoralangiography Kits Comprising The Following Items A.Femoral Sheath Insertion System 6F 11Cm B. Femoral Angiography 6F Jl4 And Jr3.5Catheters ( One Each ) C. 0.035 J Hydrophilic Teflon Wire, D.Disposable Sterile Drape For Radial / Femoral Angiography E.Disposable Sterile Gowns -2, F.Disposable Gloves-2, G.Finger Control Syringe 20Cc H.3 / 3 Rotating Manifold I.Pressure Line J.100 Ml Non-Ionic Contrast Media With320 Mg Iodine / Ml.Should Be Fda / Ce / Dcgi Approved , ( S ) Radial Angio Set With Puncture Needle, Sheath 6F 7Cm, Straight Guidewire 025 / 021And Tig Coronary Diagnosticcatheter 5F, And Hydrophilic Polymer J Tipped 035 145 Cm Wires.Should Be Fda / Ce / Dcgi Approved , ( S ) Radial Angiography Kits Comprising The Following Items A.Radial Sheath Insertion System 6F 7Cmb. Radial Angiography 5F Tig Catheter C. 0.035 J Hydrophilic Polymer Wire, D.Disposable Sterile Drape For Radial / Femoral Angiography E.Disposable Sterile Gowns -2, F.Disposable Gloves-2, G.Finger Control Syringe 20Cc H.3 / 3 Rotating Manifold I.Pressure Line J.100 Ml Non-Ionic Contrast Media 320Mg Iodine / Ml.Should Be Fda / Ce / Dcgi Approved , ( S ) Femoral Angioplasty Kit ( 1Stent ) 1. Disposable Cath-Lab Gowns Light Blue Colour Full Size And Elastic Wrist Bands With Water / Blood Impenetrable Front And Hand Shielding - 3 Nos 2.Disposable Sterile Drapes For Coronary Angiography / Angioplasty Compatible With Bilateral Femoral And Radial Approaches - 1No 3.Disposablegauze Pieces In ( Eto Sterilizable ) Packs Of 10 For Use With Cath Lab Procedures - 10Nos 4.Teflon Coated Guide Wires 145 Cms 0.035St & J - 1No 5.Arterial Pressure Monitoring Transducers ( Disposable ) - 1No 6.Initial Puncture Needles18g - 1No 7.Femoral Pci Sheath Systems Size 5F To 9Fwith Accessories For Insertion - 2Nos 8. Ptca Wire - 1 No 9.3 Ring Control Syringes For Cag / Ptca 20Cc - 1No 10. 3 / 3 Rotating Manifold For Cag / Ptca-1No 11. Touhey Borst Y Connector- Push Pull Type And Introducer Needle For Ptca - 1No 12.Ptca Guiding Catheter - 1No 13.3 Ring Finger Control Syringe 12 Cc - 1No 14.Infusion Accelerator ( Pressure Bag ) -1No 15.Rapid Exchange Balloonsystems With Semi-Compliant / Compliant Design With Excellent Trackability And High Inflation Pressures - 1No 16.Non-Compliant Balloons For Ptca - 1No 17.Drug Eluting Stents Fda / Dcgi / Ce Approved-1 No .Should Be Fda / Ce / Dcgi Approved , ( S ) Femoral Angioplasty Kit ( 2 Stent ) 1. Disposable Cath-Lab Gowns Light Blue Colour Full Size And Elastic Wrist Bands With Water / Blood Impenetrable Front And Hand Shielding - 3 Nos 2.Disposable Sterile Drapes For Coronary Angiography / Angioplasty Compatible With Bilateral Femoral And Radial Approaches - 1No 3.Disposablegauze Pieces In ( Eto Sterilizable ) Packs Of 10 For Use With Cath Lab Procedures - 10Nos 4.Teflon Coated Guide Wires 145 Cms 0.035St & J - 1No 5.Arterial Pressure Monitoring Transducers ( Disposable ) - 1No 6.Initial Puncture Needles18g - 1No 7.Femoral Pci Sheath Systems Size 5F To 9Fwith Accessories For Insertion - 2Nos 8. Ptca Wire- 1 No 9.3 Ring Control Syringes For Cag / Ptca 20Cc - 1No 10. 3 / 3 Rotating Manifold For Cag / Ptca-1No 11. Touhey Borst Y Connector- Push Pull Type And Introducer Needle For Ptca - 1No 12.Ptca Guiding Catheter - 1No 13.3 Ring Finger Control Syringe 12 Cc - 1No 14.Infusion Accelerator ( Pressure Bag ) -1No 15.Rapid Exchange Balloonsystems With Semi-Compliant / Compliant Design With Excellent Trackability And High Inflation Pressures - 1No 16.Non-Compliant Balloons For Ptca - 1No 17.Drug Eluting Stents Fda / Dcgi / Ce -2 Nos .Should Be Fda / Ce / Dcgi Approved , ( S ) Radial Angioplasty Kit ( 1 Stent ) 1. Disposable Cath-Lab Gowns Light Blue Colour Full Size And Elastic Wrist Bands With Water / Blood Impenetrable Front And Hand Shielding - 3 Nos 2.Disposable Sterile Drapes For Coronary Angiography / Angioplasty Compatible With Bilateral Femoral And Radial Approaches - 1No 3.Disposablegauze Pieces In ( Eto Sterilizable ) Packs Of 10 For Use With Cath Lab Procedures - 10Nos 4.Teflon Coated Guide Wires 145 Cms 0.035St & J - 1No 5.Arterial Pressure Monitoring Transducers ( Disposable ) - 1No 6.Initial Puncture Needles18g - 1No 7.Transradial Sheath Systems Size 6F With Accessories For Insertion - 1Nos 8. Ptca Wire - 1 No 9.3 Ring Control Syringes For Cag / Ptca 20Cc - 1No 10. 3 / 3 Rotating Manifold For Cag / Ptca-1No 11. Touhey Borst Y Connector- Push Pull Type And Introducer Needle For Ptca - 1No 12.Ptca Guiding Catheter - 1No 13.3 Ring Finger Control Syringe 12 Cc - 1No 14.Infusion Accelerator ( Pressure Bag ) -1No 15.Rapid Exchange Balloonsystems With Semi-Compliant / Compliant Design With Excellent Trackability And High Inflation Pressures - 1No 16.Non-Compliant Balloons For Ptca - 1No 17.Drug Eluting Stents Fda / Dcgi / Ce Approved -1 No .Should Be Fda / Ce / Dcgi Approved , ( S ) Radial Angioplasty Kit ( 2 Stent ) 1. Disposable Cath-Lab Gowns Light Blue Colour Full Size And Elastic Wrist Bands With Water / Blood Impenetrable Front And Hand Shielding - 3 Nos 2.Disposable Sterile Drapes For Coronary Angiography / Angioplasty Compatible With Bilateral Femoral And Radial Approaches - 1No 3.Disposablegauze Pieces In ( Eto Sterilizable ) Packs Of 10 For Use With Cath Lab Procedures - 10Nos 4.Teflon Coated Guide Wires 145 Cms 0.035St & J - 1No 5.Arterial Pressure Monitoring Transducers ( Disposable ) - 1No 6.Initial Puncture Needles18g - 1No 7.Transradial Sheath Systems Size 6F With Accessories For Insertion - 1Nos 8. Ptca Wire - 1 No 9.3 Ring Control Syringes For Cag / Ptca 20Cc - 1No 10. 3 / 3 Rotating Manifold For Cag / Ptca-1No 11. Touhey Borst Y Connector- Push Pull Type And Introducer Needle For Ptca - 1No 12.Ptca Guiding Catheter - 1No 13.3 Ring Finger Control Syringe 12 Cc - 1No 14.Infusion Accelerator ( Pressure Bag ) -1No 15.Rapid Exchange Balloonsystems With Semi-Compliant / Compliant Design With Excellent Trackability And High Inflation Pressures - 1No 16.Non-Compliant Balloons For Ptca - 1No 17.Drug Eluting Stent Fda / Dcgi / Ce Approved -2 No .Should Be Fda / Ce / Dcgi Approved , ( S ) 20Cc Inflation Deviceas One Set Capable Of Inflation Pressures Upto 30 Bar.Should Be Fda / Ce / Dcgi Approved , ( S ) 20Cc Inflation Deviceas One Set Capable Of Inflation Pressures Upto 25 Bar.Should Be Fda / Ce / Dcgi Approved , ( S ) Inflation Device To Inflate High Pressure Upto 50 Atm.Should Be Fda / Ce / Dcgi Approved , ( S ) Ptca Manifold With Flush Device.Should Be Fda / Ce / Dcgi Approved , ( S ) Infusion Accelerator ( Pressure Bag ) .Should Be Fda / Ce / Dcgi Approved , ( S ) 3 Ring Control Syringes For Cag / Ptca 12Cc.Should Be Fda / Ce / Dcgi Approved , ( S ) 3 Ring Control Syringes For Cag / Ptca 20Cc.Should Be Fda / Ce / Dcgi Approved , Guidewires , ( S ) Teflon Coated Guide Wire 145 Cm 0.021 St. Should Be Fda / Ce / Dcgi Approved , ( S ) Teflon Coated Guide Wire 145 Cm 0.021 J. Should Be Fda / Ce / Dcgi Approved , ( S ) Teflon Coated Guide Wire 145 Cm 0.025 St. Should Be Fda / Ce / Dcgi Approved , ( S ) Teflon Coated Guide Wire 145 Cm 0.025 J. Should Be Fda / Ce / Dcgi Approved , ( S ) Teflon Coated Guide Wires 145 Cm0.032St. Should Be Fda / Ce / Dcgi Approved , ( S ) Teflon Coated Guide Wires 145 Cm0.032J. Should Be Fda / Ce / Dcgi Approved , ( S ) Teflon Coated Guide Wires 145 Cms 0.035 St. Should Be Fda / Ce / Dcgi Approved , ( S ) Teflon Coated Guide Wires 145 Cms 0.035 J. Should Be Fda / Ce / Dcgi Approved , ( S ) Teflon Coated Guide Wires 145 Cms 0.038 St. Should Be Fda / Ce / Dcgi Approved , ( S ) Teflon Coated Guide Wires 145 Cms 0.038 J. Should Be Fda / Ce / Dcgi Approved , ( S ) Teflon Coated Exchange ( 260Cm And Above ) 0.018 St Peripheral Guide Wire .Should Be Fda / Ce / Dcgi Approved , ( S ) Teflon Coated Exchange ( 260Cm And Above ) 0.018 J Peripheral Guide Wire .Should Be Fda / Ce / Dcgi Approved , ( S ) Teflon Coated Exchange ( 260Cm And Above ) 0.021 St Peripheral Guide Wire .Should Be Fda / Ce / Dcgi Approved , ( S ) Teflon Coated Exchange ( 260Cm And Above ) 0.021 J Peripheral Guide Wire .Should Be Fda / Ce / Dcgi Approved , ( S ) Teflon Coated Exchange Guide Wire ( 260Cm And Above ) 0.032St.Should Be Fda / Ce / Dcgi Approved , ( S ) Teflon Coated Exchange Guide Wire ( 260Cm And Above ) 0.032 J.Should Be Fda / Ce / Dcgi Approved , ( S ) Teflon Coated Exchange Guide Wire ( 260Cm And Above ) 0.035St.Should Be Fda / Ce / Dcgi Approved , ( S ) Teflon Coated Exchange Guide Wire ( 260Cm And Above ) 0.035 J.Should Be Fda / Ce / Dcgi Approved , ( S ) Teflon Coated Exchangeguide Wire ( 260Cm And Above ) 0.038St.Should Be Fda / Ce / Dcgi Approved , ( S ) Teflon Coated Exchange Guide Wire ( 260Cm And Above ) 0.038J.Should Be Fda / Ce / Dcgi Approved , ( S ) Lunderquist Type High Support Exchange Length 0.035 ( 260Cm And Above ) Short And Long Floppy Tip Guide Wire. Should Be Fda / Ce / Dcgi Approved , ( S ) Safari Type High Support Exchange Length 0.035 ( 260Cm And Above ) Curvedtip Guide Wire. Should Be Fda / Ce / Dcgi Approved , ( S ) Confida Type Intermediatesupport Exchange Length 0.035 ( 260Cm And Above ) J Tip Guide Wire. Should Be Fda / Ce / Dcgi Approved , ( S ) Roadrunner Type Extrasupportexchange Length 0.035 ( 260Cm And Above ) Straight Tip Guide Wire With Hydrophilic Coating . Should Be Fda / Ce / Dcgi Approved , ( S ) Roadrunner Type Extrasupportexchange Length 0.035 ( 260Cm And Above ) J Tip Guide Wire With Hydrophilic Coating . Should Be Fda / Ce / Dcgi Approved , ( S ) Amplatz Superstiff Exchange Guide Wires 0.035. 260 Cm And Above- Short Floppy Tip.Should Be Fda / Ce / Dcgi Approved , ( S ) Amplatz Superstiff Exchange Guide Wires .038. 260 Cm And Above- Short Floppy Tip.Should Be Fda / Ce / Dcgi Approved , ( S ) Amplatz Ultra Stiff Exchange Guide Wires 0.035 J. 260 Cm And Above- Long Floppy Tip.Should Be Fda / Ce / Dcgi Approved , ( S ) Amplatz Ultra Stiff Exchange Guide Wires0.038J. 260 Cm And Above- Long Floppy Tip.Should Be Fda / Ce / Dcgi Approved , ( S ) Amplatz Noodle Type Exchange Guidewire Ptfe Coated Stainless Steel Wire 0.035 J. 260 Cm And Above , ( S ) Terumo Hydrophilic Guide Wires 145 Cm 018 St.Should Be Fda / Ce / Dcgi Approved , ( S ) Terumo Hydrophilic Guide Wires 145 Cm 018 J.Should Be Fda / Ce / Dcgi Approved , ( S ) Terumo Hydrophilic Guide Wires 145 Cm 021 St.Should Be Fda / Ce / Dcgi Approved , ( S ) Terumo Hydrophilic Guide Wires 145 Cm 021 J.Should Be Fda / Ce / Dcgi Approved , ( S ) Terumo Hydrophilic Guide Wires 145 Cm 025 St.Should Be Fda / Ce / Dcgi Approved , ( S ) Terumo Hydrophilic Guide Wires 145 Cm 025 J.Should Be Fda / Ce / Dcgi Approved , ( S ) Terumo Hydrophilic Guide Wires 145 Cm 032 St.Should Be Fda / Ce / Dcgi Approved , ( S ) Terumo Hydrophilic Guide Wires 145 Cm 032 J.Should Be Fda / Ce / Dcgi Approved , ( S ) Terumo Hydrophilic Guide Wires 145 Cm 035 St.Should Be Fda / Ce / Dcgi Approved , ( S ) Terumo Hydrophilic Guide Wires 145 Cm 035 J.Should Be Fda / Ce / Dcgi Approved , ( S ) Terumo Exchange Length Guide Wires 260Cm 018 St.Should Be Fda / Ce / Dcgi Approved , ( S ) Terumo Exchange Length Guide Wires 260Cm 018 J.Should Be Fda / Ce / Dcgi Approved , ( S ) Terumo Exchange Length Guide Wires 260Cm 021 St.Should Be Fda / Ce / Dcgi Approved , ( S ) Terumo Exchange Length Guide Wires 260Cm 021 J.Should Be Fda / Ce / Dcgi Approved , ( S ) Terumo Exchange Length Guide Wires 260Cm 025 St.Should Be Fda / Ce / Dcgi Approved , ( S ) Terumo Exchange Length Guide Wires 260Cm 025 J.Should Be Fda / Ce / Dcgi Approved , ( S ) Terumo Exchange Length Guide Wires 260Cm 032 St.Should Be Fda / Ce / Dcgi Approved , ( S ) Terumo Exchange Length Guide Wires 260Cm 032 J.Should Be Fda / Ce / Dcgi Approved , ( S ) Terumo Exchange Length Guide Wires 260Cm 035 St.Should Be Fda / Ce / Dcgi Approved , ( S ) Terumo Exchange Length Guide Wires 260Cm 035 J.Should Be Fda / Ce / Dcgi Approved , Guiding Catheters , ( S ) ( Ex ) Ptca Guiding Catheter 4F Jr 3.0 Curve.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 5F Jr 3.0 Curve.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 6F Jr 3.0 Curve.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 7F Jr 3.0 Curve.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 8F Jr 3.0 Curve.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 4F Jl 2.0 Curve. Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 5F Jl 2.0 Curve. Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 6F Jl 2.0 Curve. Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 7F Jl 2.0 Curve. Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 8F Jl 2.0 Curve. Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 4F Jl 3.0 Curve.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 5F Jl 3.0 Curve.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 6F Jl 3.0 Curve.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 7F Jl 3.0 Curve.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 8F Jl 3.0 Curve.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 4F Jr 3.5 Curve.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 5F Jr 3.5 Curve.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 6F Jr 3.5 Curve.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 7F Jr 3.5 Curve.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 8F Jr 3.5 Curve.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 4F Jl 3.5 Curve.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 5F Jl 3.5 Curve.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 6F Jl 3.5 Curve.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 7F Jl 3.5 Curve.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 8F Jl 3.5 Curve.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 4F Jr 4.0 Curve.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 5F Jr 4.0 Curve.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 6F Jr 4.0 Curve.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 7F Jr 4.0 Curve.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 8F Jr 4.0 Curve.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 4F Jl 4.0 Curve.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 5F Jl 4.0 Curve.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 6F Jl 4.0 Curve.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 7F Jl 4.0 Curve.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 8F Jl 4.0 Curve.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 4F Jr 4.5 Curve.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 5F Jr 4.5 Curve.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 6F Jr 4.5 Curve.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 7F Jr 4.5 Curve.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 8F Jr 4.5 Curve.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 4F Jl 4.5 Curve.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 5F Jl 4.5 Curve.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 6F Jl 4.5 Curve.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 7F Jl 4.5 Curve.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 8F Jl 4.5 Curve.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 4F Jr 5.0 Curve.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 5F Jr 5.0 Curve.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 6F Jr 5.0 Curve.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 7F Jr 5.0 Curve.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 8F Jr 5.0 Curve.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 4F Jl 5.0 Curve.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 5F Jl 5.0 Curve.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 6F Jl 5.0 Curve.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 7F Jl 5.0 Curve.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 8F Jl 5.0 Curve.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 4F Ebu 3.0 Curve.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 5F Ebu 3.0 Curve.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 5F Ebu 2.0 Curve.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 6F Ebu 2.0 Curve.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 6F Ebu 3.0 Curve.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 7F Ebu 3.0 Curve.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 8F Ebu 3.0 Curve.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 4F Ebu 3.5 Curve.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 5F Ebu 3.5 Curve.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 6F Ebu 3.5 Curve.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 7F Ebu 3.5 Curve.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 8F Ebu 3.5 Curve.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 4F Ebu 3.75 Curve.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 5F Ebu 3.75 Curve.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 6F Ebu 3.75 Curve.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 7F Ebu 3.75 Curve.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 8F Ebu 3.75 Curve.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 4F Ebu 4.0 Curve.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 5F Ebu 4.0 Curve.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 6F Ebu 4.0 Curve.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 7F Ebu 4.0 Curve.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 8F Ebu 4.0 Curve.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 4F Xb 3.0 Curve.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 5F Xb 2.5 Curve.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 5F Xb 3.0 Curve.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 6F Xb 2.5 Curve. Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 6F Xb 3.0 Curve.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 7F Xb 3.0 Curve.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 8F Xb 3.0 Curve.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 4F Xb 3.5 Curve.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 5F Xb 3.5 Curve.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 6F Xb 3.5 Curve.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 7F Xb 3.5 Curve.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 8F Xb 3.5 Curve.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Ptca Guiding Catheter 4F Xb 4.0 Curve.Should Be Fda / Ce / Dcgi Approved , ( Ex ) Ptca Guiding Catheter 5F Xb 4.0 Curve.Should Be Fda / Ce / Dcgi Approved , ( Ex ) Ptca Guiding Catheter 6F Xb 4.0 Curve.Should Be Fda / Ce / Dcgi Approved , ( Ex ) Ptca Guiding Catheter 7F Xb 4.0 Curve.Should Be Fda / Ce / Dcgi Approved , ( Ex ) Ptca Guiding Catheter 8F Xb 4.0 Curve.Should Be Fda / Ce / Dcgi Approved , ( Ex ) Ptca Guiding Catheter 4F Mp All Curves.Should Be Fda / Ce / Dcgi Approved , ( Ex ) Ptca Guiding Catheter 5F Mp All Curves.Should Be Fda / Ce / Dcgi Approved , ( Ex ) Ptca Guiding Catheter 6F Mp All Curves.Should Be Fda / Ce / Dcgi Approved , ( Ex ) Ptca Guiding Catheter 7F Mp All Curves.Should Be Fda / Ce / Dcgi Approved , ( Ex ) Ptca Guiding Catheter 8F Mp All Curves.Should Be Fda / Ce / Dcgi Approved , ( Ex ) Ptca Guiding Catheter 4F Cls 3.0.Should Be Fda / Ce / Dcgi Approved , ( Ex ) Ptca Guiding Catheter 5F Cls 3.0Should Be Fda / Ce / Dcgi Approved , ( Ex ) Ptca Guiding Catheter 6F Cls 3.0.Should Be Fda / Ce / Dcgi Approved , ( Ex ) Ptca Guiding Catheter 7F Cls 3.0.Should Be Fda / Ce / Dcgi Approved , ( Ex ) Ptca Guiding Catheter 8F Cls 3.0.Should Be Fda / Ce / Dcgi Approved , ( Ex ) Ptca Guiding Catheter 4F Cls 3.5.Should Be Fda / Ce / Dcgi Approved , ( Ex ) Ptca Guiding Catheter 5F Cls 3.5Should Be Fda / Ce / Dcgi Approved , ( Ex ) Ptca Guiding Catheter 6F Cls 3.5.Should Be Fda / Ce / Dcgi Approved , ( Ex ) Ptca Guiding Catheter 7F Cls 3.5.Should Be Fda / Ce / Dcgi Approved , ( Ex ) Ptca Guiding Catheter 8F Cls 3.5.Should Be Fda / Ce / Dcgi Approved , ( Ex ) Ptca Guiding Catheter 4F Al 0.75.Should Be Fda / Ce / Dcgi Approved , ( Ex ) Ptca Guiding Catheter 5F Al 0.75Should Be Fda / Ce / Dcgi Approved , ( Ex ) Ptca Guiding Catheter 6F Al 0.75.Should Be Fda / Ce / Dcgi Approved , ( Ex ) Ptca Guiding Catheter 7F Al 0.75.Should Be Fda / Ce / Dcgi Approved , ( Ex ) Ptca Guiding Catheter 8F Al 0.75.Should Be Fda / Ce / Dcgi Approved , ( Ex ) Ptca Guiding Catheter 4F Al 1.0.Should Be Fda / Ce / Dcgi Approved , ( Ex ) Ptca Guiding Catheter 5F Al 1.0Should Be Fda / Ce / Dcgi Approved , ( Ex ) Ptca Guiding Catheter 6F Al 1.0.Should Be Fda / Ce / Dcgi Approved , ( Ex ) Ptca Guiding Catheter 7F Al 1.0.Should Be Fda / Ce / Dcgi Approved , ( Ex ) Ptca Guiding Catheter 8F Al 1.0.Should Be Fda / Ce / Dcgi Approved , ( Ex ) Ptca Guiding Catheter 4F Al 1.5.Should Be Fda / Ce / Dcgi Approved , ( Ex ) Ptca Guiding Catheter 5F Al 1.5.Should Be Fda / Ce / Dcgi Approved , ( Ex ) Ptca Guiding Catheter 6F Al 1.5.Should Be Fda / Ce / Dcgi Approved , ( Ex ) Ptca Guiding Catheter 7F Al 1.5.Should Be Fda / Ce / Dcgi Approved , ( Ex ) Ptca Guiding Catheter 8F Al 1.5.Should Be Fda / Ce / Dcgi Approved , ( Ex ) Ptca Guiding Catheter 4F Al 2.0.Should Be Fda / Ce / Dcgi Approved , ( Ex ) Ptca Guiding Catheter 5F Al 2.0.Should Be Fda / Ce / Dcgi Approved , ( Ex ) Ptca Guiding Catheter 6F Al 2.0.Should Be Fda / Ce / Dcgi Approved , ( Ex ) Ptca Guiding Catheter 7F Al 2.0.Should Be Fda / Ce / Dcgi Approved , ( Ex ) Ptca Guiding Catheter 8F Al 2.0.Should Be Fda / Ce / Dcgi Approved , ( Ex ) Ptca Guiding Catheter 4F Ar 1.0.Should Be Fda / Ce / Dcgi Approved , ( Ex ) Ptca Guiding Catheter 5F Ar 1.0.Should Be Fda / Ce / Dcgi Approved , ( Ex ) Ptca Guiding Catheter 6F Ar 1.0.Should Be Fda / Ce / Dcgi Approved , ( Ex ) Ptca Guiding Catheter 7F Ar 1.0.Should Be Fda / Ce / Dcgi Approved , ( Ex ) Ptca Guiding Catheter 8F Ar 1.0.Should Be Fda / Ce / Dcgi Approved , ( Ex ) Ptca Guiding Catheter 4F Ar 2.0.Should Be Fda / Ce / Dcgi Approved , ( Ex ) Ptca Guiding Catheter 5F Ar 2.0.Should Be Fda / Ce / Dcgi Approved , ( Ex ) Ptca Guiding Catheter 6F Ar 2.0.Should Be Fda / Ce / Dcgi Approved , ( Ex ) Ptca Guiding Catheter 7F Ar 2.0.Should Be Fda / Ce / Dcgi Approved , ( Ex ) Ptca Guiding Catheter 8F Ar 2.0.Should Be Fda / Ce / Dcgi Approved , ( Ex ) 6F 3D Rdc Guiding Catheter .Should Be Fda / Ce / Dcgi Approved , ( Ex ) 7F 3D Rdc Guiding Catheter .Should Be Fda / Ce / Dcgi Approved , ( Ex ) 4F Radial Tig 4.0 Ptca Guiding Catheter.Should Be Fda / Ce / Dcgi Approved , ( Ex ) 5F Radial Tig 4.0 Ptca Guiding Catheter.Should Be Fda / Ce / Dcgi Approved , ( Ex ) 6F Radial Tig 4.0 Ptca Guiding Catheter.Should Be Fda / Ce / Dcgi Approved , ( Ex ) 7F Radial Tig 4.0 Ptca Guiding Catheter.Should Be Fda / Ce / Dcgi Approved , ( Ex ) 4F Radial Tig 4.5 Ptca Guiding Catheter.Should Be Fda / Ce / Dcgi Approved , ( Ex ) 5F Radial Tig 4.5 Ptca Guiding Catheter.Should Be Fda / Ce / Dcgi Approved , ( Ex ) 6F Radial Tig 4.5 Ptca Guiding Catheter.Should Be Fda / Ce / Dcgi Approved , ( Ex ) 7F Radial Tig 4.5 Ptca Guiding Catheter.Should Be Fda / Ce / Dcgi Approved , ( Ex ) 4F Ikari Left 3.5 Ptca Guiding Catheter.Should Be Fda / Ce / Dcgi Approved , ( Ex ) 5F Ikari Left 3.5 Ptca Guiding Catheter.Should Be Fda / Ce / Dcgi Approved , ( Ex ) 6F Ikari Left 3.5 Ptca Guiding Catheter.Should Be Fda / Ce / Dcgi Approved , ( Ex ) 7F Ikari Left 3.5 Ptca Guiding Catheter.Should Be Fda / Ce / Dcgi Approved , ( Ex ) 4F Ikari Left 3.75 Ptca Guiding Catheter.Should Be Fda / Ce / Dcgi Approved , ( Ex ) 5F Ikari Left 3.75 Ptca Guiding Catheter.Should Be Fda / Ce / Dcgi Approved , ( Ex ) 6F Ikari Left 3.75 Ptca Guiding Catheter.Should Be Fda / Ce / Dcgi Approved , ( Ex ) 7F Ikari Left 3.75 Ptca Guiding Catheter.Should Be Fda / Ce / Dcgi Approved , ( Ex ) 4F Ikari Left 4.0 Ptca Guiding Catheter.Should Be Fda / Ce / Dcgi Approved , ( Ex ) 5F Ikari Left 4.0 Ptca Guiding Catheter.Should Be Fda / Ce / Dcgi Approved , ( Ex ) 6F Ikari Left 4.0 Ptca Guiding Catheter.Should Be Fda / Ce / Dcgi Approved , ( Ex ) 7F Ikari Left 4.0 Ptca Guiding Catheter.Should Be Fda / Ce / Dcgi Approved , ( Ex ) 4F Ikari Left 4.5 Ptca Guiding Catheter.Should Be Fda / Ce / Dcgi Approved , ( Ex ) 5F Ikari Left 4.5 Ptca Guiding Catheter.Should Be Fda / Ce / Dcgi Approved , ( Ex ) 6F Ikari Left 4.5 Ptca Guiding Catheter.Should Be Fda / Ce / Dcgi Approved , ( Ex ) 7F Ikari Left 4.5 Ptca Guiding Catheter.Should Be Fda / Ce / Dcgi Approved , ( Ex ) 4F Ikari Right 1.0 Ptca Guiding Catheter.Should Be Fda / Ce / Dcgi Approved , ( Ex ) 5F Ikari Right 1.0 Ptca Guiding Catheter.Should Be Fda / Ce / Dcgi Approved , ( Ex ) 6F Ikari Right 1.0 Ptca Guiding Catheter.Should Be Fda / Ce / Dcgi Approved , ( Ex ) 7F Ikari Right 1.0 Ptca Guiding Catheter.Should Be Fda / Ce / Dcgi Approved , ( Ex ) 4F Ikari Right 1.5 Ptca Guiding Catheter.Should Be Fda / Ce / Dcgi Approved , ( Ex ) 5F Ikari Right 1.5 Ptca Guiding Catheter.Should Be Fda / Ce / Dcgi Approved , ( Ex ) 6F Ikari Right 1.5 Ptca Guiding Catheter.Should Be Fda / Ce / Dcgi Approved , ( Ex ) 7F Ikari Right 1.5 Ptca Guiding Catheter.Should Be Fda / Ce / Dcgi Approved , ( Ex ) 4F Ikari Right 2.0 Ptca Guiding Catheter.Should Be Fda / Ce / Dcgi Approved , ( Ex ) 5F Ikari Right 2.0 Ptca Guiding Catheter.Should Be Fda / Ce / Dcgi Approved , ( Ex ) 6F Ikari Right 2.0 Ptca Guiding Catheter.Should Be Fda / Ce / Dcgi Approved , ( Ex ) 7F Ikari Right 2.0 Ptca Guiding Catheter.Should Be Fda / Ce / Dcgi Approved , ( Ex ) 5F Kimmy Ptca Guiding Catheter.Should Be Fda / Ce / Dcgi Approved , ( Ex ) 6F Kimmyptca Guiding Catheter.Should Be Fda / Ce / Dcgi Approved , ( Ex ) 5F Kimmy Minor Ptca Guiding Catheter.Should Be Fda / Ce / Dcgi Approved , ( Ex ) 6F Kimmy Minor Ptca Guiding Catheter.Should Be Fda / Ce / Dcgi Approved , ( S ) Sheathless Ptca Guiding Catheter For Coronary Interventions From Radial Access 5F. Should Be Fda / Ce / Dgci Approved , ( S ) Sheathless Ptca Guiding Catheter For Coronary Interventions From Radial Access 6F. Should Be Fda / Ce / Dgci Approved , ( S ) Sheathless Ptca Guiding Catheter For Coronary Interventions From Radial Access 7F. Should Be Fda / Ce / Dgci Approved , ( S ) Sheathless Ptca Guiding Catheter For Coronary Interventions From Radial Access 8F. Should Be Fda / Ce / Dgci Approved , ( S ) Coronary Guide Extension Catheter 8 Fr .Should Be Fda / Ce / Dcgi Approved , ( S ) Coronary Guide Extension Catheter With Distal 2 Mm Radioluscent Tip Capable Of Doing Oct In Coronary Ostial Lesion.Should Be Fda / Ce / Dcgi Approved , ( S ) Superselective Cathether For Mother And Child Technique.Should Be Fda Or Ce And Dcgi Approved , ( S ) Coronary Guide Extension Catheter 6Fr. Should Be Fda / Ce / Dcgi Approved , ( S ) Coronary Guide Extension Catheter 7Fr. Should Be Fda / Ce / Dcgi Approved , ( S ) Soft Guideliner System For Mother And Child Technique. Should Be Fda Or Ce And Dcgi Approved , Coronary Wires , ( S ) Ptca Wires Floppy Standard Length .Should Be Fda / Ce / Dcgi Approved , ( S ) Ptca Wires Floppy Extra Supportexchange Length.Should Be Fda / Ce / Dcgi Approved , ( S ) Ptca Wires Floppy Extra Supportintermediate Standard Length.Should Be Fda / Ce / Dcgi Approved , ( S ) Ptca Wires Floppy Extra Support Standard Length.Should Be Fda / Ce / Dcgi Approved , ( S ) Ptca Doc Link Extension Floppy Extra Supportwires.Should Be Fda / Ce / Dcgi Approved , ( S ) Floppy Extra Support Exchange Wires For Ptca .Should Be Fda / Ce / Dcgi Approved , ( S ) Double Core Spring Tip Core To Tip Floppy Extra Support Type Wires For Ptca.Should Be Fda / Ce / Dcgi Approved , ( S ) Ptca Wires Floppy Extra Supporttapering Tip Hydrophilic.Should Be Fda / Ce / Dcgi Approved , ( S ) Ptca Wire - Floppy Extra Support Cto Wires-Platinum.Should Be Fda / Ce / Dcgi Approved , ( S ) Ptca Wires Cto- Hydrophobicfloppy Extra Support.Should Be Fda / Ce / Dcgi Approved , ( S ) Ptca Wires For Cto-Hydrophlic Without Polymer Coatingfloppy Extra Supportextra Support.Should Be Fda / Ce / Dcgi Approved , ( S ) Ptca Wires Polymer Coated Hydrophilic Floppy Extra Support .Should Be Fda / Ce / Dcgi Approved , ( S ) Ptca Wires Polymer Coated Hydrophilic Floppy Extra Support.Should Be Fda / Ce / Dcgi Approved , ( S ) Ptca Wires- Polymer Coated Floppy Extra Support Tapering Tip.Should Be Fda / Ce / Dcgi Approved , ( S ) Ptca Wires - Specially Designed Floppy Extra Supportfor Tortuous Vessels.Should Be Fda / Ce / Dcgi Approved , ( S ) Ptca Wires Floppy Extra Support Hybrid Coated.Should Be Fda / Ce / Dcgi Approved , ( S ) Ptca Wires Floppy Extra Support Extrasupport Polymer Coated.Should Be Fda / Ce / Dcgi Approved , ( S ) Link Extension Floppy Extra Support Ptca Wire Type 300 Cm Wires.Should Be Fda / Ce / Dcgi Approved , ( S ) Ptca 009 Exchange Length Floppy Wires For Retrograde Approach Exchange Length.Should Be Fda / Ce / Dcgi Approved , ( S ) Ptca Wire For Cto Hydrophobic Straight With Tip Loads Available Upto 12 Gm.Should Be Fda / Ce / Dcgi Approved , ( S ) Ptca Wire For Collateral Crossing With Tip Load Of 0.3 Gm.Should Be Fda / Ce / Dcgi Approved , ( S ) Ptca Wire For Cto Hydrophilic With A Uncoated Distal Tip, Preshaped.Should Be Fda / Ce / Dcgi Approved , ( S ) Ptca 009 Exchange Length Floppy Extra Support Wires For Retrograde Approach Exchange Length.Should Be Fda / Ce / Dcgi Approved , Coronary Balloons , ( S ) ( Ex ) Rapid Exchange Balloonsystems With Semi-Compliant Design With Excellent Trackability And High Inflation Pressures All Sizes.Should Be Fda Anddcgi Approved , ( S ) ( Ex ) Rapid Exchange Balloonsystems With Compliant Design With Excellent Trackability And High Inflation Pressures All Sizes .Should Be Fda Anddcgi Approved , ( S ) ( Ex ) Rapid Exchange Balloonsystems With Short Overhang And Semi-Compliant Design With Excellent Trackability And High Inflation Pressures All Sizes .Should Be Ce Anddcgi Approved , ( S ) ( Ex ) Rapid Exchange Balloonsystems With Short Overhang Compliant Design With Excellent Trackability And High Inflation Pressures All Sizes .Should Be Ce Anddcgi Approved , ( S ) ( Ex ) Rapid Exchange Balloonsystems Low Profile With Semi-Compliant Design With Excellent Trackability And High Inflation Pressures All Sizes.Should Be Fda Anddcgi Approved , ( S ) ( Ex ) Rapid Exchange Balloonsystems With Low Profile Compliant Design With Excellent Trackability And High Inflation Pressures All Sizes .Should Be Fda Anddcgi Approved , ( S ) ( Ex ) Rapid Exchange Non-Compliant Balloons For Ptca Of Fibroticlesions All Sizes.Should Be Fda And Dcgi Approved , ( S ) ( Ex ) Rapid Exchange Non-Compliant Balloons For Ptca Of Calcific Lesions All Sizes.Should Be Fda And Dcgi Approved , ( S ) ( Ex ) Rapid Exchange Non-Compliant Balloons For Ptca Of Fibrotic Lesions With Short Overhang All Sizes.Should Be Fda And Dcgi Approved , ( S ) ( Ex ) Rapid Exchange Non-Compliant Balloons For Ptca Of Calcific Lesions With Short Overhangall Sizes.Should Be Fda And Dcgi Approved , ( S ) ( Ex ) Rapid Exchange Non-Compliant Balloons Low Profile For Ptca Of Fibroticlesions All Sizes.Should Be Fda And Dcgi Approved , ( S ) ( Ex ) Rapid Exchange Non-Compliant Balloons Low Profile For Ptca Of Calcific Lesions All Sizes.Should Be Fda And Dcgi Approved , ( S ) ( Ex ) Rapid Exchange Non-Compliant High-Pressure Balloons For Ptca All Sizes.Should Be Fda And Dcgi Approved , ( S ) ( Ex ) Rapid Exchange Non-Compliant Ultrahigh Pressure Balloon For Calcific Lesions ( 30 Atm And Above For Ptca ) All Sizes .Should Be Fda And Dcgi Approved , ( S ) ( Ex ) Rapid Exchange Non-Compliant Nominal Pressure Balloon For Cto Intervention Of All Sizes.Should Be Fda And Dcgi Approved , ( S ) ( Ex ) Rapid Exchange Non-Compliant High Pressure Balloon For Cto Intervention All Sizes.Should Be Fda And Dcgi Approved , ( S ) ( Ex ) Rapid Exchange Non-Compliant Ultrahigh Pressure Balloon For Cto Intervention All Sizes.Should Be Fda And Dcgi Approved , ( S ) ( Ex ) Rapid Exchange Non-Compliant Balloons For Ptca All Sizes.Should Be Ce Anddcgi Approved , ( S ) ( Ex ) Rapid Exchange Ultra High Pressure ( Upto 35Atm ) Non-Compliant Balloons For Ptca.Should Be Fda And Dcgi Approved , ( S ) ( Ex ) Rapid Exchange Ultra High Pressure ( Upto 45Atm ) Non-Compliant Balloons For Ptca.Should Be Ce Anddcgi Approved , ( S ) ( Ex ) Ultra Low Profile Non Compliant Balloons For Pci.Should Be Ce And Dcgi Approved , ( S ) ( Ex ) Ultra Low Profile Compliant Balloons For Pci.Should Be Ce And Dcgi Approved , ( S ) ( Ex ) Ultra Low Profile Semi Complaint Baloons For Pci.Should Be Ce And Dcgi Approved , ( S ) ( Ex ) Low Profile Cto Baloons For Pci0.65Mm In Diameter.Should Be Ce And Dcgi Approved , ( S ) ( Ex ) Low Profile Cto Baloons For Pci0.75Mm In Diameter.Should Be Ce And Dcgi Approved , ( S ) ( Ex ) Over The Wire Balloons For Ptca Compliant .Should Be Fda Or Ce And Dcgi Approved , ( S ) ( Ex ) Over The Wire Balloons For Ptca Semicompliant .Should Be Fda Or Ce And Dcgi Approved , ( S ) ( Ex ) Over The Wire Balloons For Ptca Semicompliant For Cto .Should Be Fda Or Ce And Dcgi Approved , ( S ) ( Ex ) Over The Wire Balloons For Ptca Non-Compliant .Should Be Fda Or Ce And Dcgi Approved , ( S ) ( Ex ) Over The Wire Balloons For Ptca Noncompliant For Cto .Should Be Fda Or Ce And Dcgi Approved , ( S ) ( Ex ) Over The Wire Balloons For Ptsma.Should Be Fda Or Ce And Dcgi Approved , ( S ) ( Ex ) Cutting Balloons Coronary.Should Be Fda Or Ce And Dcgi Approved , ( S ) ( Ex ) Scoring Coronary Balloonsfor Severely Calcified Lesions.Should Be Fda Or Ce And Dcgi Approved , ( S ) ( Ex ) Drug Elutingcoronary Balloons For In Stent Restenosis Coronary Paclitaxel Eluting Should Be Fda Or Ce And Dcgi Approved , ( S ) ( Ex ) Dedicated Non Compliant Coronary Balloon For Proximal Optimisation Technique ( Pot Balloon ) With Shoulder Length Of 0.6 Mm Or Less. Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Coronary Perfusion Balloon Catheter.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Drug Elutingcoronary Balloons For In Stent Restenosis Coronary Sirolimuseluting Should Be Fda Or Ce And Dcgi Approved , Coronary Stents , ( S ) ( Ex ) Balloon Expandablebare Metalcobalt Chromium Alloy Coronary Stents .Should Be Fda Or Ce And Dcgi Approved , ( S ) ( Ex ) Balloon Expandable Sirolimus Eluting Second Generation Coronary Stents.Should Be Fda Or Ce And Dcgi Approved , ( S ) ( Ex ) Balloon Expadable Everolimus Eluting Second Generation Coronary Stents.Should Be Fda Or Ce And Dcgi Approved , ( S ) ( Ex ) Balloon Expadable Zoratolimus Eluting Second Generation Coronary Stents.Should Be Fda Or Ce And Dcgi Approved , ( S ) ( Ex ) Balloon Expadable Sirolimus Eluting Third Generation Coronary Stents.Should Be Fda Or Ce And Dcgi Approved , ( S ) ( Ex ) Balloon Expadable Everolimus Eluting Third Generation Coronary Stents.Should Be Fda Or Ce And Dcgi Approved , ( S ) ( Ex ) Balloon Expadable Zotarolimus Eluting Third Generation Coronary Stents.Should Be Fda Or Ce And Dcgi Approved , ( S ) ( Ex ) Balloon Expandablesirolimuscoatedcobalt Chromium Alloy Less Than 70Micrometer Strutcoronary Stents .Should Be Fda Or Ce And Dcgi Approved , ( S ) ( Ex ) Balloon Expandablesirolimuscoatedcobalt Chromium Alloy More Than 70Micrometer Strut Coronary Stents .Should Be Fda Or Ce And Dcgi Approved , ( S ) ( Ex ) Balloon Expandableeverolimuscoatedcobalt Chromium Alloy Less Than 70Micrometer Strutcoronary Stents .Should Be Fda Or Ce And Dcgi Approved , ( S ) ( Ex ) Balloon Expandableeverolimuscoatedcobalt Chromium Alloy Morethan 70Micrometer Strutcoronary Stents .Should Be Fda Or Ce And Dcgi Approved , ( S ) ( Ex ) Balloon Expandablezotarolimuscoatedcobalt Chromium Alloy Less Than 70Micrometer Strutcoronary Stents .Should Be Fda Or Ce And Dcgi Approved , ( S ) ( Ex ) Balloon Expandablezotarolimuscoatedcobalt Chromium Alloy More Than 70Micrometer Strutcoronary Stents .Should Be Fda Or Ce And Dcgi Approved , ( S ) ( Ex ) Balloon Expandablebiolimuscoatedcobalt Chromium Alloy Less Than 70Micrometer Strutcoronary Stents .Should Be Fda Or Ce And Dcgi Approved , ( S ) ( Ex ) Balloon Expandablebiolimuscoatedcobalt Chromium Alloy Morethan 70Micrometer Strutcoronary Stents .Should Be Fda Or Ce And Dcgi Approved , ( S ) ( Ex ) Balloon Expandablesirolimuscoatedplatinum Chromium Alloy Coronary Stents .Should Be Fda Or Ce And Dcgi Approved , ( S ) ( Ex ) Balloon Expandableeverolimuscoatedplatinum Chromium Alloy Coronary Stents .Should Be Fda Or Ce And Dcgi Approved , ( S ) ( Ex ) Balloon Expandablezotarolimuscoatedplatinum Chromium Alloy Coronary Stents .Should Be Fda Or Ce And Dcgi Approved , ( S ) ( Ex ) Balloon Expandablebiolimuscoatedplatinum Chromium Alloy Coronary Stents .Should Be Fda Or Ce And Dcgi Approved , ( S ) ( Ex ) Balloon Expandablesirolimuscoatedplatinum Iridium Alloy Coronary Stents .Should Be Fda Or Ce And Dcgi Approved , ( S ) ( Ex ) Balloon Expandableeverolimuscoatedplatinum Iridium Alloy Coronary Stents .Should Be Fda Or Ce And Dcgi Approved , ( S ) ( Ex ) Balloon Expandablezotarolimuscoatedplatinum Iridium Alloy Coronary Stents .Should Be Fda Or Ce And Dcgi Approved , ( S ) ( Ex ) Balloon Expandablebiolimuscoatedplatinum Iridium Alloy Coronary Stents .Should Be Fda Or Ce And Dcgi Approved , ( S ) ( Ex ) Balloon Expandablesirolimuscoatedpolymer Free Coronary Stents .Should Be Fda Or Ce And Dcgi Approved , ( S ) ( Ex ) Balloon Expandableeverolimuscoatedpolymer Freecoronary Stents .Should Be Fda Or Ce And Dcgi Approved , ( S ) ( Ex ) Balloon Expandablezotarolimuscoatedpolymer Freecoronary Stents .Should Be Fda Or Ce And Dcgi Approved , ( S ) ( Ex ) Balloon Expandablebiolimuscoatedpolymer Free Coronary Stents .Should Be Fda Or Ce And Dcgi Approved , ( S ) ( Ex ) Balloon Expandablesirolimuscoatedbiodegradable Polymer Coronary Stents .Should Be Fda Or Ce And Dcgi Approved , ( S ) ( Ex ) Balloon Expandableeverolimuscoatedbiodegradable Polymer Coronary Stents .Should Be Fda Or Ce And Dcgi Approved , ( S ) ( Ex ) Balloon Expandablezotarolimuscoatedbiodegradable Polymer Coronary Stents .Should Be Fda Or Ce And Dcgi Approved , ( S ) ( Ex ) Balloon Expandablebiolimuscoatedbiodegradable Polymer Coronary Stents .Should Be Fda Or Ce And Dcgi Approved , ( S ) ( Ex ) Drug Eluting Stents Ceand Dcgi Approved.Should Be Ce And Dcgi Approved , ( S ) ( Ex ) Drug Eluting Stents Dcgi Approved.Should Be Dcgi Approved , ( S ) ( Ex ) Drug Eluting Coronary Stents Tapering.Should Be Fda Or Ce And Dcgi Approved , ( S ) ( Ex ) Drug Eluting Coronary Stents Extra Length ( Beyond 38Mm ) .Should Be Fda Or Ce And Dcgi Approved , ( S ) ( Ex ) Drug Eluting Stents- Polymer Free.Should Be Fda Or Ce And Dcgi Approved , ( S ) ( Ex ) Drug Eluting Stents- Sizes Above 48Mm For Diffuse Lesions.Should Be Fda Or Ce And Dcgi Approved , ( S ) ( Ex ) Drug Eluting Coronary Stents 4 And 4.5Mm Diamater Expandable At Least To5.75 All Lengths.Should Be Fda Or Ce And Dcgi Approved , ( S ) ( Ex ) Drug Eluting Stent Mounted On Drug Coated Balloon.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Drug Eluting Bioresorbable Vascular Scaffold System For Coronaries.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Covered Stents-Coronary Cobalt Chromium 5F Guiding Compatible Low Profile All Sizes.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Covered Stents-Coronary Cobalt Chromium6f Guiding Compatible Low Profile All Sizes.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Covered Stents-Coronary Stainless Steel6f Guiding Compatible Low Profile All Sizes.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Covered Stents-Coronary Stainless Steel7f Guiding Compatible Low Profile All Sizes.Should Be Fda / Ce / Dcgi Approved , Thrombus Extraction , ( S ) ( Ex ) Thrombus Extraction Catheters For Primary Ptca Without Stillette.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Thrombus Extraction Catheters For Coronary Thrombus Extraction Floppy Soft Tip Without Stillette.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Thrombus Extraction Catheters For Primary Ptca With Stillette .Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Thrombus Extraction Catheters For Primary Ptca Without Stillette.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Thrombus Extraction Catheters For Peripheral Venous / Pulmonary Thrombi 8F With A Suction Device Provided By The Company On Demand .Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Thrombus Extraction Catheters For Peripheral Arterial-Venous Thrombi 6F With A Suction Device Provided By The Company On Demand .Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Thrombus Extraction Catheters For Peripheral Arterial Thrombi4f With A Suction Device Provided By The Company On Demand .Should Be Fda / Ce / Dcgi Approved , Microcatheter , ( D ) Coronary Microcatheters ( 0.014 Compatable ) With Distal Entry Profile 1.8F.Should Be Fda Or Ce Anddcgi Approved , ( D ) Coronary Microcatheters ( 0.014 Compatable ) With Distal Entry Profile 1.8F Floppy Tip .Should Be Fda Or Ce Anddcgi Approved , ( D ) Coronary Microcatheters ( 0.014 Compatable ) With Distal Entry Profile 1.4F.Should Be Fda Or Ce Anddcgi Approved , ( D ) Coronary Microcatheters ( 0.014 Compatable ) With Distal Entry Profile 1.4F Floppy Tip.Should Be Fda Or Ce Anddcgi Approved , ( D ) Coronary Microcatheters For Cto Entry- Braided With Cutting Tip.Should Be Fda Or Ce Anddcgi Approved , ( D ) Coronary Microcatheters Torquable ( 0.014 Compatable ) .Should Be Fda Or Ce Anddcgi Approved , ( D ) Dual Lumen Coronarymicroguide Catheters For Sidebranch Entry ( Over The Wire And Monorail ) .Should Be Fda Or Ce And Dcgi Approved , ( D ) Angled Tip Coronary Microcatheter For Side Branch Access.Should Be Fda Or Ce Anddcgi Approved , ( D ) Retrograde Coronary Collateral Channel Dilator .Should Be Fda Or Ce And Dcgi Approved , ( D ) Peripheral Micro Catheters For Visceral Angio Embolisation-Should Be Hydrophilic And 0.021 Compatable.Should Be Fda Or Ce And Dcgi Approved , ( D ) Peripheral Micro Catheters For Visceral Angio Embolisation-Should Be Hydrophilic With Attached 0.018 Hydrophilic Wire.Should Be Fda Or Ce And Dcgi Approved , Imaging & Physiology , ( D ) Intravascular Ultrasound Catheters Compatiblewith Volcano Ivus System .Should Be Fda / Ce / Dcgi Approved , ( D ) Intravascular Ultrasound Catheters Compatiblewith Ilab Ivus System With Pull Back Sled.Should Be Fda / Ce / Dcgi Approved , ( D ) Intravascular Ultrasound Catheters Compatible With Ilab Ivus System.Should Be Fda / Ce / Dcgi Approved , ( D ) Oct Catheters .Should Be Fda / Ce / Dcgi Approved , ( D ) Ffr Wires Compatible With Abbott Ffr Systems.Should Be Fda / Ce / Dcgi Approved , ( D ) Ffr Wires Wireless, Compatible With Abbott Ffr Systems.Should Be Fda / Ce / Dcgi Approved , ( D ) Ffr Wires Compatible With Volcano Ffr System .Should Be Fda / Ce / Dcgi Approved , ( D ) Ffr Wire Compatible With Boston Ffr System.Should Be Fda / Ce / Dcgi Approved , Cto Pci , ( Ex ) Ultra Low Profile Semi Compliant Coronary Balloons For Chronic Total Occlusions.Should Be Fda / Ce / Dcgi Approved , ( Ex ) Dissection Re Entry Balloon For Coronary Cto.Should Be Fda / Ce / Dcgi Approved , ( Ex ) Sub Intimal Tracking Device For Cto.Should Be Fda / Ce / Dcgi Approved , Debulking Systems Coronary , ( D ) Rotablator Wire 009 Floppy.Should Be Fda / Ce / Dcgi Approved , ( D ) Rotablator Wire 009 Extra Support .Should Be Fda / Ce / Dcgi Approved , ( D ) ( Ex ) Rotational Atherectomy Burrall Sizes , ( D ) Rotational Atherectomy Advancer , ( D ) ( Ex ) Rotational Atherectomy Burr And Advancer System Integrated All Sizes , ( D ) ( Ex ) Coronary Orbital Atherectomy System For Calcified Coronary Lesions All Sizes.Should Be Fda / Ce / Dcgi Approved , ( D ) ( Ex ) Coronary Laser Atherectomy Catheter For Intervention In Calcified Coronaries All Sizes.Should Be Ce And Dcgi Approved , ( D ) ( Ex ) Coronary Intravascular Lithrotripsy Balloons For Heavy Calcified Proximal Vessel Pci All Sizes.Should Be Ce And Dcgi Approved , Iabp , ( D ) ( Ex ) Intra Aortic Balloon Pump Balloons Small, Medium And Large Sizes Compatible With Datascope Iabp Systems.Should Be Fda / Ce / Dcgi Approved. , ( D ) Helium With Tank For Iabp Machine Datascope Model. , Baloon Valvuloplasty , ( S ) ( Ex ) All Sizes Of Ptmc Balloons- Reusable.Should Be Fda / Ce / Dcgi Approved , ( S ) Accessories For Ptmc Balloons.Should Bece And Dcgi Approved, The Accessories Will Be Procured From The Same Company Is Selected For Ptmc Balloons . Accessories Include A ) Coiled La Guide Wire For Tracking The Balloon Into La B ) 21F Black Dilatorc ) Lv Entry Wire D ) Metal Stretching Tube E ) Stylet F ) Syringe For Inflation G ) Ruler / Calliper For Measuring Balloon Size , ( D ) ( Ex ) All Sizes Of Ptmc Balloons With Accessories- Reusable.Should Be Fda / Ce / Dcgi Approved , ( D ) ( Ex ) All Sizes Of Mitral Valve Balloon Dilatation Systems With Reusable Latex Rubber Balloon Design And Accessories Are To Be Quoted. Should Be Fda / Ce / Dcgi Approved , ( D ) ( Ex ) All Sizes Of Mitral Valve Balloon Dilatation Systems With Reusable Latex Rubber Balloon Design. Should Be Fda, Ce / Dcgi Approved , ( D ) ( Ex ) Accessories For Mitral Valve Balloon Dilatation Systems With Reusable Latex Rubber Balloon Design . The Accessories Will Be Procured From The Same Company Is Selected For Mitral Valve Balloon Dilatation Systems With Reusable Latex Rubber Balloon Design.A ) Coiled La Guide Wire For Tracking The Balloon Into La B ) 21F Black Dilatorc ) Lv Entry Wire D ) Metal Stretching Tube E ) Stylet F ) Syringe For Inflation G ) Ruler / Calliper For Measuring Balloon Size Should Be Fda, Ce / Dcgi Approved , ( D ) ( Ex ) Aortic Valvuloplasty Balloon Systems With Accessories Of All Sizes And Lengths.Should Be Fda / Ce / Dcgi Approved , ( D ) ( Ex ) Pulmonary Valvuloplasty Balloon Systems With Accessories All Sizs And Lengths .Should Be Ce / Dcgi Approved , ( D ) ( Ex ) Stepped Diameter Balloons Cribier- Letac With Accessories All Sizes And Lengths.Should Be Fda / Ce / Dcgi Approved , ( D ) ( Ex ) Pediatric Valvuloplasty Tyshak Mini 014 Compatible Balloons With Accelerator, Bifoil Balloons, Trifoil Balloons With Accessories All Sizes.Should Be Fda / Ce / Dcgi Approved , ( D ) ( Ex ) Pediatric Valvuloplasty Tyshak-Ii Balloons With Accelerator, Bifoil Balloons With Accessories All Sizes.Should Be Fda / Ce / Dcgi Approved , ( D ) ( Ex ) Pediatric Valvuloplasty Tyshak-Ii Balloons With Accelerator, Trifoil Balloons With Accessories All Sizes.Should Be Fda / Ce / Dcgi Approved , ( D ) ( Ex ) Low Profile Non-Compliant Pediatric Valvuloplasty Balloons 4-10 Mm Diameter, With Introducer Size Starting At 4 Fr With Accessories.Should Be Fda / Ce / Dcgi Approved , Peripheral Intervention , ( S ) Balkan Contralateral Sheath 6F.Should Be Fda / Ce / Dcgi Approved , ( S ) Balkan Contralateral Sheath 7F.Should Be Fda / Ce / Dcgi Approved , ( S ) Balkan Contralateral Sheath 8F.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) High Pressure Non Compliant Peripheral Balloons- ( Sizes From 4Mm-10Mm ) 0.035 Compatable ( All Lengths ) .Should Be Ce And Dcgi Approved , ( S ) ( Ex ) Cutting Balloons Peripheral. 6Mm To 8Mm Diamter All Lengths Should Be Fda Or Ce And Dcgi Approved , ( S ) ( Ex ) Scoring Balloons - Peripheral- For Severely Calcified Lesions.Should Be Fda Or Ce And Dcgi Approved , ( S ) ( Ex ) Drug Eluting Balloons Peripheral.Should Be Fda Or Ce And Dcgi Approved , ( S ) ( Ex ) Drug Eluting Balloons Peripheral For Isr .Should Be Fda Or Ce And Dcgi Approved , ( S ) ( Ex ) Ultra High Pressure Mustang Type Balloons Peripheral- Sizes From 4Mm To 10Mm All Lengths..Should Be Fda Or Ce And Dcgi Approved , ( Ex ) Covered Self Expanding Covered Stent Grafts For Peripheral Anurysm And Leaks ( 4Mm To 12Mm ) .Should Be Fda Or Ce Anddcgi Approved , ( S ) Left Internal Mammary Guide Catheter5f, 6F And & 7F .Should Be Fda / Ce / Dcgi Approved , ( S ) Braided Multipurpose Guide Caths ( 5F And 6F ) .Should Be Fda / Ce / Dcgi Approved , ( S ) Soft Tipped Braided Guide Catheters For ( 4F, 5F ) For Coronary / Visceral Use.Should Be Fda Or Ce And Dcgi Approved , ( S ) Braided Simmons Shaped Cerebral Caths.Should Be Fda / Ce / Dcgi Approved , ( S ) Renal Double Curve Guide Catheter 4F, 5F80cm , 120 Cm, 140 Cm.Should Be Fda / Ce / Dcgi Approved , ( S ) Renal Double Curve Guide Catheter 4F, 5F80cm , 120 Cm, 140 Cm.Should Be Fda / Ce / Dcgi Approved , ( S ) Renal Double Curve Guide Catheter 6F80cm , 120 Cm, 140 Cm.Should Be Fda / Ce / Dcgi Approved , ( S ) Renal Double Curve Guide Catheter 7F80cm, 120 Cm, 140 Cm.Should Be Fda / Ce / Dcgi Approved , ( S ) Terumo Glide Catheter Head Hunter 4F.Should Be Fda / Ce / Dcgi Approved , ( S ) Terumo Glide Catheterhead Hunter 5F And 6 F.Should Be Fda / Ce / Dcgi Approved , ( S ) Terumo Glide Catheter Cobra 4F.Should Be Fda / Ce / Dcgi Approved , ( S ) Terumo Glide Catheter 4F.Should Be Fda / Ce / Dcgi Approved , ( S ) Yashiro Glide Catheter5f 6F80 Cm, 120 Cm, 140 Cm.Should Be Fda / Ce / Dcgi Approved , ( S ) Yashiro Glide Catheter 4F80 Cm, 120 Cm, 140Cm.Should Be Fda / Ce / Dcgi Approved , ( Ex ) Peripheral Balloons ( 0.035 Compatable ) For Femoro Popliteal And Iliac Lesions.Should Be Fda / Ce / Dcgi Approved , ( S ) Fogarty Arterial Embolectomy Catheter 4&5F.Should Be Fda / Ce / Dcgi Approved , ( Ex ) Renal Balloon ( 0.014 Compatable ) .Should Be Fda / Ce / Dcgi Approved , ( Ex ) Carotid And Btk Balloons ( 0.014 Compatable ) .Balloon Shaft Length Should Be160 Cmand Above.Should Be Fda / Ce / Dcgi Approved , ( Ex ) Small Vessel Balloon ( Diameters Should Be From 1Mm To 4Mm ) All Lengths.Should Be Fda / Ce / Dcgi Approved , ( Ex ) Periph / Renal / Carotid Guiding-100 Cm And Longer.Should Be Fda / Ce / Dcgi Approved , ( Ex ) Renal Stents -0.014 Compatable Balloon Mounted Shaft Length 80 Cm- All Sizes.Should Be Fda / Ce / Dcgi Approved , ( Ex ) Self Expanding Femoro Popliteal Stents - All Diameters.Should Be Fda / Ce / Dcgi Approved , ( Ex ) Dilators Of Coons Type For Serial Vascular Dilation For Large Access .Should Be Ce And Dcgi Approved , ( Ex ) Balloon Expandable Stents Peripheral- All Sizes.Should Be Fda / Ce / Dcgi Approved , ( Ex ) Self Expanding Iliac Stents - All Diameters.Should Be Fda Or Ce And Dcgi Approved , ( Ex ) Carotid Distal Protection Devices.Should Be Fda / Ce / Dcgi Approved , ( Ex ) Carotid Stents Taperingself Expanding.Should Be Fda / Ce / Dcgi Approved , ( Ex ) Carotid Stentsstraight Self Expanding.Should Be Fda / Ce / Dcgi Approved , ( Ex ) Stent Grafts For Visceral Vascular System ( Should Be Highy Trackable, 0.035 Compatable ) .Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Sizing Balloons For Asd / Pda.Should Be Fda / Ce / Dcgi Approved , ( S ) Peripheral Guide Wires& Speciality Wires Exchange Length ( 0.018 ) .Should Be Fda / Ce / Dcgi Approved , ( S ) Peripheral Guide Wires& Speciality Wires Exchange Length ( 0.035 ) .Should Be Fda / Ce / Dcgi Approved , ( S ) Road Runner Polymer Coated Wire 035 Staright And J.Should Be Fda / Ce / Dcgi Approved , Peripheral Intravascular Lithotripsy Catheter For Treating Calcified Lesions In Peripheral Arteries Like Illiac, Femoral And Popliteal Artery.Should Be Fda / Ce / Dcgi Approved , Highly Flexible Kink Resitant Peripheral Stents Suitable For Deploying In Superficial Femoral Artery And Poplliteal Artery.Should Be Fda / Ce / Dcgi Approved , ( S ) Peripheral Chronic Total Occlusion Wires 0.014, 0.0.35 Diameter.Should Be Fda / Ce / Dcgi Approved , Renal Denervation , Renal Artery Denervation Catheter System For Management Of Resistant Hypertension. Should Be Fda / Ce / Dgci Approved , Embolization , ( S ) ( Ex ) Cyanoacrylate Glue For Sealing Coronary Perforation.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Embolisation Particles Poly Vinyl Alcohol All Sizes.Should Be Fda / Ce / Dcgi Approved , ( S ) Lipoidol For Embolization Should Be Fda / Ce / Dcgi Approved , ( S ) Super Absorbant Polymer Microspheres For Drug ( Doxorubucin ) Adsorption For Tace.Should Be Fda / Ce / Dcgi Approved , ( S ) Gelfoam ( Powder Or Granule Form ) For Embolization.Should Be Fda / Ce / Dcgi Approved , ( S ) N-Butyl Cyanoacrylate Glue For Embolization .Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Microcatheters With Inbuilt Hydrophilic Wire For Peripheral Angiography And Particle / Coil Delivery.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Microcatheters - Steerable / Shapable With Inbuilt Hydrophilic Wire For Peripheral Angiography And Particle / Coil Delivery.Should Be Fda / Ce / Dcgi Approved , ( S ) Gel Foam Powder For Angio Embolisation.Should Be Fda Or Ce And Dcgi Approved , ( Ex ) Embolization Coils 035 All Sizes.Should Be Fda / Ce / Dcgi Approved , ( Ex ) Embolization Coils 0.038 To 052 All Sizes.Should Be Fda / Ce / Dcgi Approved , ( Ex ) Embolization Coils 052 All Sizes.Should Be Fda / Ce / Dcgi Approved , ( Ex ) Embolization Micro Coils 018 All Sizes - Non Detachable And Freely Deliverable.Should Be Fda / Ce / Dcgi Approved , ( Ex ) Embolization Micro Coils 018 All Sizes -Detachable 2D.Should Be Fda / Ce / Dcgi Approved , ( S ) Embolization Coils Highly Trackable 0.018 Embolisation Coils For Post Op- Visceral ( Gi And Renal Artery Pseudoaneurysm ) .Should Be Ce And Dcgi Approved , ( Ex ) Embolization Micro Coils 018 All Sizes -Detachable 3D.Should Be Fda / Ce / Dcgi Approved , ( Ex ) Nitinol Vascular Plugs For Embolisation.Should Be Fda / Ce / Dcgi Approved , Ex ) Bi Lobed Nitinol Vascular Plugs For Embolisation.Should Be Fda / Ce / Dcgi Approved , Ex ) Tri Lobed ( Should Have Retention Disk On Both Sides ) Nitinol Vascular Plugs For Embolisation.Should Be Fda / Ce / Dcgi Approved , Ex ) Nitinol Vascular Plugs For Embolisation Deliverable Through Smallest Fr Diagnostic Catheter Supporting 0.038 Guidewire .Should Be Fda / Ce / Dcgi Approved , Snares , ( Ex ) Endovascular Snares With Metal Tip.Should Be Fda / Ce / Dcgi Approved , ( Ex ) Endovascular Snares With Polymer Tip.Should Be Fda / Ce / Dcgi Approved , ( Ex ) Endovascular Snares Gooseneck. Should Be Fda / Ce / Dcgi Approved , ( Ex ) Endovascular Snares Needle Eye. Should Be Fda / Ce / Dcgi Approved , ( S ) Coronary Micro Snares.Should Be Ce And Dcgi Approved , ( Ex ) Endovascular Snares Basket. Should Be Fda / Ce / Dcgi Approved , Coarctation Stenting , ( D ) ( Ex ) Bare Aortic Stents For Coarctation ( Sizes Should Be Above 20Mm Up To 40Mm ) - Baloon Expandable Design.Should Be Fda / Ce / Dcgi Approved , ( D ) ( Ex ) Non Pre-Mounted Bare Aortic Stents With Semi-Open Cell Design Made Of Cobalt-Chromium With Specially Designed Links For Non-Foreshortening On Balloon-Dilatation With Low Crimping Profile Capable Ofbeing Deliverable Through Sheath Sizes Starting From 9F. , ( D ) ( Ex ) Non Pre-Mounted Eptfe Covered Aortic Stents With Semi-Open Cell Design Made Of Cobalt-Chromium With Specially Designed Links For Non-Foreshortening On Balloon-Dilatation With Low Crimping Profile Capable Ofbeing Deliverable Through Sheath Sizes Starting From 12F Or Smaller.Capable Of Being Expanded To Sizes Starting From 14 Mm To More Than Or Equal To 22 Mm , ( D ) ( Ex ) Non Pre-Mounted Bare Aortic Stents With Semi-Open Cell Design Made Of Cobalt-Chromium With Minimum Foreshortening On Balloon-Dilatation With Low Crimping Profile Capable , ( D ) ( Ex ) Non Pre-Mounted Bare Aortic Stents With Semi-Open Cell Design Made Of Cobalt-Chromium With Minimum Foreshortening On Balloon-Dilatation With Low Crimping Profile , ( D ) ( Ex ) Premounted Eptfe Covered Stents Made Of Cobalt-Chromium Made For Aortic Coarctation Stenting With Low Foreshortening On Dilatation Capable Of Being Expanded From 12 To 24 Mm Capable Of Being Delivered Through Sheath Sizes Starting From 9 F , ( D ) ( Ex ) Premounted Eptfe Covered Stents Made Of Cobalt-Chromium With Low Foreshortening On Dilatation Capable Of Being Expanded From 5Mm To 10 Mm Capable Of Being Delivered Through Sheath Sizes Starting From 6F Meant For Use In Peripheral Vessels, Renal Artery, Arteriovenous Fistulas For Dialysis Etc , ( D ) ( Ex ) Non-Premounted Bare Aortic Stents Made Of Platinum-Iridium Capable Of Being Expanded From 8Mm To 24 Mm Capable Of Being Delivered Through Sheath Sizes Starting From 9F Meant For Use In Aorta , ( D ) ( Ex ) Non-Premounted Ptfe Covered Aortic Stents Made Of Platinum-Iridium Capable Of Being Expanded From 8Mm To 24 Mm Capable Of Being Delivered Through Sheath Sizes Starting From 12F Meant For Use In Aorta , ( D ) ( Ex ) Bare Aortic Stents For Coarctation ( Sizes Should Be Above 12 To 20 Mm ) - Baloon Expandable Design.Should Be Fda / Ce / Dcgi Approved , ( D ) ( Ex ) Bare Aortic Stents For Coarctation ( Sizes Should Be Above 20Mm Up To 40Mm ) - Self-Expanding Design.Should Be Fda & Dcgi Approved , ( D ) ( Ex ) Bare Aortic Stents For Coarctation ( Sizes Should Be Above 12 To 20 Mm ) - Self Expanding Design.Should Be Fda & Dcgi Approved , ( D ) ( Ex ) Covered Aortic Stents ( Balloon Expandable Only ) For Aortic Coarctation ( Sizes From 12 To 30Mm ) . Should Bece And Dcgi Approved. , ( D ) ( Ex ) Balloon In Balloon Stent Placement Catheter For Aortic Coarcation ( Sizes From 12 To 30Mm ) . Should Bece And Dcgi Approved. , ( D ) ( Ex ) Covered Mounted Aortic Stents ( Balloon Expandable Only ) For Aortic Coarctation ( Sizes From 12 To 30Mn ) . Should Bece And Dcgi Approved , Device Closure Accessories , ( S ) Mullins Sheath With Matching Dilator Withsidearm 6Fall Sizes.Should Be Fda / Ce / Dcgi Approved ( Length To Be Specified ) , ( S ) Mullins Sheath With Matching Dilator Withsidearm 7Fall Sizes.Should Be Fda / Ce / Dcgi Approved ( Length To Be Specified ) , ( S ) Mullins Sheath With Matching Dilator Withsidearm 8Fall Sizes.Should Be Fda / Ce / Dcgi Approved ( Length To Be Specified ) , ( S ) Mullins Sheath With Matching Dilator Withsidearm 9Fall Sizes.Should Be Fda / Ce / Dcgi Approved ( Length To Be Specified ) , ( S ) Mullins Sheath With Matching Dilator Withsidearm 10Fall Sizes.Should Be Fda / Ce / Dcgi Approved ( Length To Be Specified ) , ( S ) Mullins Sheath With Matching Dilator Withsidearm 11Fall Sizes.Should Be Fda / Ce / Dcgi Approved ( Length To Be Specified ) , ( S ) Mullins Sheath With Matching Dilator Withsidearm 12Fall Sizes.Should Be Fda / Ce / Dcgi Approved ( Length To Be Specified ) , ( S ) Mullins Sheath With Matching Dilator Withsidearm 14Fall Sizes.Should Be Fda / Ce / Dcgi Approved ( Length To Be Specified ) , ( S ) Mullins Sheath With Matching Dilator Withsidearm 16Fall Sizes.Should Be Fda / Ce / Dcgi Approved ( Length To Be Specified ) , ( S ) 5F Flexible Delivery Sheaths With Steerable And Deflectable Introducer Systems For Asd / Vsd / Pda Device Closure .Should Be Fda / Ce And Dcgi Approved , ( S ) 6Fflexible Delivery Sheaths With Steerable And Deflectable Introducer Systems For Asd / Vsd / Pda Device Closure .Should Be Fda / Ce And Dcgi Approved , ( S ) 8F Flexible Delivery Sheaths With Steerable And Deflectable Introducer Systems For Asd / Vsd / Pda Device Closure .Should Be Fda / Ce And Dcgi Approved , ( S ) 10F Flexible Delivery Sheaths With Steerable And Deflectable Introducer Systems For Asd / Vsd / Pda Device Closure .Should Be Fda / Ce And Dcgi Approved , ( S ) 12F Flexible Delivery Sheaths With Steerable And Deflectable Introducer Systems For Asd / Vsd / Pda Device Closure .Should Be Fda / Ce And Dcgi Approved , ( S ) 14F Flexible Delivery Sheaths With Steerable And Deflectable Introducer Systems For Asd / Vsd / Pda Device Closure .Should Be Fda / Ce And Dcgi Approved , ( Ex ) Cook Sheaths ( All Sizes 6F-7F ) With Check Flo Valves ) With Angled Tips For Asd Device Delivery.Should Be Fda Or Ce And Dcgi Approved , ( Ex ) Cook Sheaths ( All Sizes 8F-9F ) With Check Flo Valves ) With Angled Tips For Asd Device Delivery.Should Be Fda Or Ce And Dcgi Approved , ( Ex ) Cook Sheaths ( All Sizes 10F-11F ) With Check Flo Valves ) With Angled Tips For Asd Device Delivery.Should Be Fda Or Ce And Dcgi Approved , ( Ex ) Cook Sheaths ( All Sizes 12F-13F ) With Check Flo Valves ) With Angled Tips For Asd Device Delivery.Should Be Fda Or Ce And Dcgi Approved , ( Ex ) Cook Sheaths ( All Sizes 14F-15F ) With Check Flo Valves ) With Angled Tips For Asd Device Delivery.Should Be Fda Or Ce And Dcgi Approved , ( Ex ) Cook Sheaths ( All Sizes 16F ) With Check Flo Valves ) With Angled Tips For Asd Device Delivery.Should Be Fda Or Ce And Dcgi Approved , ( Ex ) Ultra Compliant Linear Sizing Balloons With Markers For Asd Balloon Sizing ( 18Mm, 24Mm 34Mm ) .Should Be Ce / Dcgi Approved , ( Ex ) Haursdorf Delivery Sheaths For Asd Device Closure All Sizes. Should Be Fda / Ce / Dcgi Approved , Atrial Septal Devices , ( Ex ) Asd Devices: Allcustomised Sizes From 8Mm To 50 Mm.Should Befda / Ce And Dcgi Approved ( Device Only ) , ( Ex ) Delivery Cable For Asd Device 5F / 6F For Sizes 8Mm To 50Mm ( The Cable Will Be Procured From The Same Company Who Is Selected As L1 In The Category : Asd Devices: Allcustomised Sizes From 8Mm To 50 Mm Should Befda, Ce And Dcgi Approved As Indicated In The Row Above , ( ( Ex ) Asd Devices: Allcustomised Sizes From 8Mm To 50 Mm.Should Befda / Ce And Dcgi Approved ( Device Only ) , ( Ex ) Delivery Cable For Asd Devices: Allcustomised Sizes From 4 Mm Waist Diameter Onwards ( The Cable Will Be Procured From The Same Company Which Is Selected As L1 In The Category Asd Devices: Allcustomised Sizes From 8Mm To 50 Mm.Should Befda & Ce And Dcgi Approved As Indicated In The Row Above , ( Ex ) Asd Devices Allcustomised Sizes From 8Mm To 50 Mm With Delivery Cable And Delivery System ( Loading Sheath And Long Sheath For Device Delivery ) : All Customised Sizes From 8Mm To 50 Mm.Should Befda / Ce And Dcgi Approved , ( Ex ) Asd Devices Allcustomised Sizes From 8Mm To 50 Mm With Delivery Cable And Delivery System ( Loading Sheath And Long Sheath For Device Delivery ) : All Customised Sizes From 8Mm To 50 Mm.Should Befda &Ce And Dcgi Approved , ( Ex ) Fenestrated Asd Device For Mutiple Septal Defects With Cable And Accesories All Sizes.Should Be Fda / Ce / Dcgi Approved , ( Ex ) Asd Amplatzer Type Self Centre Devices With All Sizes From 8Mm And Above .Should Be Fda Approved , ( Ex ) Atrial Septal Occluder ( Self-Centering ) For Complex Morphology With Balloon-Assisted Delivery With Cable And Accesories.Should Be Fda Or Ce Anddcgi Approved , ( Ex ) Purple Recovery Sheaths For Embolised Asd Devices-16 F And Above Size.Should Be Fda Approved , ( Ex ) Large Sized Atrial Septal Occluders Above 40Mm Size With Delivery Sheath And Cables.Should Bece And Dcgi Approved , ( Ex ) Dual Disc Nitinol Biocompatable Layer Coated Secundum Type Atrial Occluders ( All Sizses ) With Pre Assembled Delivery System.Should Be Fda Or Ce Anddcgi Approved , ( Ex ) Cribriform Multifenestrated Septal Occluder With A Narrow Waist -Various Sizes; Disc Diameters Upto 40 Mm Meant For Occlusion Of Multifenestrated Asds. Should Be Fda / Ce / Dgci Approved , ( Ex ) Atrial Flow Regulator Device With Delivery Cable And Accesories.Should Be Fda / Ce / Dgci Approved , ( Ex ) Patent Foramen Ovale ( Pfo ) Closure Device With Delivery Cable And Accesories.Should Be Fda / Ce / Dgci Approved , Pda Devices , ( D ) ( Ex ) Pda Occusion Device --All Customisable Sizes From 3Mm To 20Mm Waist Size .Should Be Fda / Ce / Dcgi Approved ( Device Only ) , ( D ) ( Ex ) Delivery Cable For Pda Occlusion Device ( The Cable Will Be Procured From The Same Company Who Is Selected As L1 In The Category Pda Occusion Device --All Customisable Sizes From 3Mm To 20Mm Waist Size .Should Be Fda / Ce / Dcgi Approved , ( Ex ) Pda Occusion Device --All Customisable Sizes With From 4Mm To 20Mm Waist Size . 4X6 Device Should Be Deliverable By 5Fr Delivery System.Should Be Fda&Ce / Dcgi Approved ( Device Only ) , ( Ex ) Delivery Cable Set For Pda Occlusion Device ( The Cable Will Be Procured From The Same Company That Is Selected As L1 In The Category Pda Occlusion Device --All Customisable Sizes From 4Mm To 20Mm Waist Size. 4X6 Device Should Be Deliverable By 5Fr Delivery System. Should Be Fda&Ce / Dcgi Approved , ( Ex ) Pda Occusion Device --All Customisable Sizes With From 3Mm To 20Mm Waist Size With Delivery Cable.Should Be Fda / Ce / Dcgi Approved , ( Ex ) Pda Occusion Device --All Customisable Sizes With From 3Mm To 20Mm Waist Size With Delivery Cable.Should Be Fda&Ce / Dcgi Approved , ( Ex ) Ado-1 Device With Delivery Cable For All Morphology.Should Be Fda Or Ce Anddcgi Approved , ( Ex ) Duct Occlusion Device With Delivery System Nontaperingsheaths With Sidearm+Introducer Cable Set .Should Be Fda / Ce / Dcgi Approved , ( Ex ) Pda Occusion Device With Dual Discs Of Equal Size And Delivery Cable.Should Be Fda Or Ce Anddcgi Approved , ( Ex ) Pda Delivery Systems And Introducer Cable Systems .Should Be Fda / Ce / Dcgi Approved. , ( Ex ) Low Profile Duct Occluder Device For Neonates And Infantswith Delivery Cable And 4F Delivery Systems. Should Befda / Ce And Dcgi Approved , ( Ex ) Low Profile Duct Occluder Device For Neonates Compatible With 4F Delivery System.Should Be Fda Ce And Dcgi Approved ( Device Only ) , ( D ) Delivery Cable And 4F Sheath ( The Cable And Sheath Will Be Procured From The Same Company Who Is Selected As L1 In The CategoryLow Profile Duct Occluder Device For Neonates And Infants Compatible With 4F Delivery System , ( Ex ) Single Disc Duct Occluders With With Sizes From 3Mm Onwards Up To 20 Mm ..Should Be Fda Or Ce Anddcgi Approved ( Device Alone ) , ( D ) ( Ex ) Delivery Cable For Single Disk Duct Occluders ( The Cablewill Be Procured From The Same Company Who Is Selected As L1 In The CategorySingle Disc Duct Occluders With Sizes From 3Mm Onwards Up To 20 Mm ..Should Be Fda Or Ce And Dcgi Approved , Vsd Devices , ( Ex ) Ventricular Septal Defect Closure Devices All Sizes ( 4Mm To18 Mm ) .Should Be Fda / Ce / Dcgi Approved ( Device Only ) , ( Ex ) Delivery Cable Ventricular Septal Defect Closure ( The Cablewill Be Procured From The Same Company Who Is Selected As L1 In The Category- Ventricular Septal Defect Closure Devices All Sizes ( 4Mm To18 Mm ) .Should Be Fda / Ce / Dcgi Approved , ( Ex ) Muscular Vsd Closure Devices-All Sizes With Delivery Cable - Cost Of Cable And Device Should Be Mentioned Separately.Should Be Fda / Ce / Dcgi Approved , ( Ex ) Low Profile Delivery Sheathfor Vsd Closure Devices ( 5F To 14F ) .Should Be Ce And Dcgi Approved , ( Ex ) Ventricular Septal Defect Closure Devices All Sizes With Delivery System And Delivery Cable.Should Be Fda / Ce And Dcgi Approved , ( Ex ) Ventricular Septal Defect Closure Devices ( Only Device ) All Sizes .Should Be Fda / Ce And Dcgi Approved , ( Ex ) Delivery Cable For The Item Ventricular Septal Defect Closure Devices ( Only Device ) All Sizes.Should Be Fda / Ce And Dcgi Approved ( The Cable Will Be Procured From The Same Company Who Is Selected As L1 In The Item Mentioned Above , ( Ex ) Post Infarct Ventricular Septal Rupture Closure Devices- All Sizes And Types.Fda Approved , ( Ex ) Ventricular Septal Defect ( Device Alone ) For Antegrade Closure .Should Be Fda Or Ce And Dcgi Approved , ( Ex ) Extra Soft Nitinol Multi-Functional Closure Devices ( Only Device ) Compatible With Guide Catheter And Delivery Cables Attachable To Both Ends Of The Device.Deliverable With A Minimum Of Atleast 4Fr Delivery System .Should Be Ce / Dcgi Approved , ( S ) 4 F And 5 F Catheter Compatable Peri Membraneuous Vsd Device With Double Screw Design For Antegrade And Retrograde Closure ( Device Only ) .Should Bece And Dcgi Approved , ( S ) ( Ex ) Braided Kink Resistant Long ( 100-120Cm ) Delivery Sheaths For Vsd Closure All Sizes.Should Be Fda / Ce / Dcgi Approved , ( S ) ( Ex ) Cook Long Sheaths Capable Of Asd / Vsd / Pda Device Delivery Sizes 6Fto 16F.Should Be Fda / Ce / Dcgi Approved , La Appendage Exclusion , ( D ) ( Ex ) Left Atrial Appendage Closure Device With Delivery System All Sizes.Should Be Fda / Ce / Dcgi Approved , Transcatheter Valve Replacement & Repair , ( Ex ) Trans Catheter Aortic Valve ( Self-Expanding ) With Delivery Systems And All Accessories .Should Be Fda / Ce / Dcgi Approved , ( Ex ) Trans Catheter Aortic Valve ( Balloon Expanding ) With Delivery Systems And All Accessories.Should Be Fda / Ce / Dcgi Approved , ( Ex ) Trans Catheter Aortic Valve Delivery Sheath ( For Self Expanding ) .Should Be Fda / Ce / Dcgi Approved , ( Ex ) Trans Catheter Aortic Valve Delivery Sheath ( Balloon Expanding ) .Should Be Fda / Ce / Dcgi Approved , ( Ex ) Transcatheter Mitral Valve Repair System With Accessories.Should Be Fda / Ce / Dcgi Approved , ( Ex ) Transcatheter Tricuspid Valve Repair System With Accessories.Should Be Fda / Ce / Dcgi Approved , ( Ex ) Percutaneous Bicaval Self Expanding Valve System For Severe Tricuspid Regurgitation With Accessories. Should Be Fda / Ce / Dcgi Approved , ( Ex ) Transcatheter Balloon Expandable Pulmonary Valve With Delivery System. Should Be Fda / Ce / Dgci Approved , ( Ex ) Transcatheter Self Expanding Pulmonary Valve With Delivery System. Should Be Fda / Ce / Dgci Approved , ( Ex ) Large Bore Long Femoral Sheaths 12-18 F For Aortic / Tavi Interventions.Should Be Fda / Ce / Dcgi Approved , Tevar / Evar , ( Ex ) Large Diameter ( 14-20Mm ) Balloon Expanding Aortic / Vena Caval Stents.Should Be Fda / Ce / Dcgi Approved , ( Ex ) Coda Balloon For Optimalaortic Stent Expansion .Should Be Fda Or Ce And Dcgi Approved , ( Ex ) Anzel Sheaths For Fenestarted Evar .Should Be Fda / Ce / Dcgi Approved , ( Ex ) Balloon Expandable Covered Stents ( Sizes 5-20Mm ) For Fenestrated Tevar / Evar.Should Be Fda / Ce / Dcgi Approved , ( Ex ) Expandable Femoral Sheaths For Balloon Expandable Valves .Should Be Fda / Ce / Dcgi Approved , ( Ex ) Braided Kink Resistant Flexible Sheaths ( 60-100Cm ) For Fenestarted Tevar And Carotid Interventions-Straight And Curved.Should Be Fda / Ce / Dcgi Approved , ( Ex ) Large Diametercovered Aorta-Arch And Zone 2Stent Grafts Taa All Sizes.Should Be Fda / Ce / Dcgi Approved , ( Ex ) Aorto Uni Iliac Stent Coveredgrafts All Sizes.Should Bece And Dcgi Approved , ( Ex ) Aortic Stent Covered Graftsfor Dta Aneurysm Stenting .Should Be Fda / Ce / Dcgi Approved , ( Ex ) Low Profile Dacron / Ptfe Covered Stent Grafts ( 20-45Mm ) For Sealing Extensive Aortic Dissection .Should Bece And Dcgi Approved , ( Ex ) Low Profile Hydrophilic Sheaths For Aortic Procedures ( 12 F And Above ) .Should Be Fda / Ce / Dcgi Approved , ( Ex ) Covered Stent Grafts For Aortic Arch Aneurysm Withonsite Fenestraion Capability.Should Be Fda / Ce / Dcgi Approved , ( Ex ) Aortic Covered Stent Grafts ( Straight ) Capable For Fenestration For Justa Renal And Juxta Subclavain Aneurysms And Traumatic Aortic Injury.Should Be Fda / Ce / Dcgi Approved , ( Ex ) Abdominal Aortic Aneurysm Stent Grafts With Iliac Limbs For Abd Aorta Aneurysm.Should Be Fda / Ce / Dcgi Approved , Special Catheters & Implants , Impella Catheter For Percutaneous Cardiopulmonary Support 2.5 Lpm , Impella Catheter For Percutaneous Cardiopulmonary Support 5 Lpm , ( Ex ) Large Bore Low Profile Manual Aspiration System For High Thrombus Load From Peripheral Arteries / Veins .Should Be Fda / Ce / Dcgi Approved , ( S ) Bioptomes For Endomyocardial Biopsy :Bioptomes ; 5.2F .Should Be Fda / Ce / Dcgi Approved , ( Ex ) Bioptome For Endomyocardial Biopsy 6F.Should Be Fda / Ce / Dcgi Approved , ( S ) Swan Ganz Capable Of Accommodating 0.038 Guide Wire Large Lumen Size7f .Should Be Fda / Ce / Dcgi Approved , ( S ) Swan Ganz Capable Of Accommodating 0.032 / 035 Guide Wire Large Lumen Size6f .Should Be Fda / Ce / Dcgi Approved , ( S Balloon Atrial Septostomy Catheter.Should Be Fda / Ce / Dcgi Approved , ( D ) Vena Cava Filter- Retrivable, Jugular Deployement.Should Be Fda / Ce / Dcgi Approved , ( D ) Vena Cava Filter- Retrivable, Femoral Deployement.Should Be Fda / Ce / Dcgi Approved , ( D ) Vena Cava Filter- Retrival System .Should Be Fda / Ce / Dcgi Approved , Intracardiac Echocardiography Catheter Is Compatible With Ilab Echo System. , Intracardiac Echocardiography Catheter Compatible With Philips Echo System. , Trans Septal Puncture , Ssir - Single Chamber Rate Responsive Implantable Multiprogrammable Pacemakerwith Maximum Programmable Sensitivity Of 0.5 Mv Or More With Matching Leads And Subclavian Introducer Set To Be Quoted As One Set. Active Fixation Leads Should Be Supplied As Atrial ( 50% ) / Ventricular ( 50% ) .Should Be Fda / Ce / Dcgi Approved , Vdd Implantable Multiprogrammable Pacemaker With Shortest Programmable Av Delay Of 50 Ms, With Matching Single Pass Steroid Eluting Vdd Lead And Matching Sublavian Introducer. .Should Be Fda / Ce / Dcgi Approved , Ddd - Dual Chamber Implantable Multiprogrammable Pacemaker With Shortest Programmable Av Delay Of 50 Ms, With Matching Set Of Steroid Eluting Active Fixation Atrial And Ventricular Leads And Two Matching Subclavian Introducers..Should Be Fda / Ce / Dcgi Approved , Dddr - Dual Chamber Rate-Responsive Implantable Multiprogrammable Pacemaker Withshortest Programmable Av Delay Of 50 Ms, With Matching Set Of Steroid Eluting Active Fixation Atrial And Ventricular Leads And Two Matching Subclavian Introducers..Should Be Fda / Ce / Dcgi Approved , Bipolar Lead Specially Designed For Placement In Coronary Sinus For Lv Pacing. Should Be Supplied With 9F Short Sheath With Valve, Long Preshaped Slittable Sheaths In Various Shapes For Cs Cannulation And Inner Subselective Sheath. Lead, Long Sheath, Subselective Sheath And Short Sheath Should Be Quoted As One Set..Should Be Fda / Ce / Dcgi Approved , Cath Lab Injectables , ( S ) Contrast Media For Angiography And Angioplasty ( Non-Ionic 350 Mg I / Ml, 100 Ml Bottles ) .Should Be Fda / Ce / Dcgi Approved , ( S ) Contrast Media For Angiography And Angioplasty ( Non-Ionic 350 Mg I / Ml, 50 Ml Bottles ) .Should Be Fda / Ce / Dcgi Approved , ( S ) Iso Osmolar Contrast Media For Angiography And Angioplasty For Patients With Renal Dysfunction ( Non-Ionic 320 Mg I / Ml, 100 Ml Bottles ) .Should Be Fda / Ce / Dcgi Approved , ( S ) Iso Osmolar Contrast Media For Angiography And Angioplasty For Patients With Renal Dysfunction ( Non-Ionic 320 Mg I / Ml 50 Ml Bottles ) .Should Be Fda / Ce / Dcgi Approved , ( S ) Myocardial Echocardiographic Contrast Comprising Of Sulphur Hexachloride Or Equivalent Micro Bubbles.Should Be Fda / Ce / Dcgi Approved , Inj Tirofiban 100 Ml Bottles.Should Be Fda / Ce / Dcgi Approved , Injection Sildenafil 10 Mg Vial.Should Be Fda / Ce / Dcgi Approved , Injection Nicorandil 48 Mg Vial.Should Be Fda / Ce / Dcgi Approved , Injection Nicorandil 2 Mg Vial.Should Be Fda / Ce / Dcgi Approved , Injection Milrenone 10 Mg Vial. Should Be Fda / Ce / Dcgi Approved , Injection Cangrelor 50 Mg Vial. Should Be Fda / Ce / Dcgi Approved , Injection Bivaluridin 250 Mg Vial .Should Be Fda / Ce / Dcgi Approved , Injection Tenectaplase 30Mg Should Be Fda / Ce / Dcgi Approved , Injection Tenectaplase 40Mg Should Be Fda / Ce / Dcgi Approved , Injection Tenectaplase 50Mg Should Be Fda / Ce / Dcgi Approved , Biomarkers , ( D ) Troponin Iquantitative Bed Side Test Kit .Should Be Fda / Ce / Dcgi Approved Measuring Device To Be Supplied , ( D ) Troponin Tquantitative Bed Side Test Kit.Should Be Fda / Ce / Dcgi Approved Measuring Device To Be Supplied , ( D ) High Sensitive Troponin T Quantitive Quantitative Bed Side Test Kit.Should Be Fda / Ce / Dcgi Approved Measuring Device To Be Supplied , ( D ) High Sensitive Troponin I Quantitative- Fda Approved-Analyser Should Be Supplied.Should Be Fda Approved Measuring Device To Be Supplied , ( D ) N-Terminal Pro Bnp Quantitative Bed Side Test Kit.Should Be Fda / Ce / Dcgi Approved Measuring Device To Be Supplied , ( D ) N-Terminalbnpquantitative Bed Side Test Kit.Should Be Fda / Ce / Dcgi Approved Measuring Device To Be Supplied , ( D ) D-Timer Quantitative Bed Side Test Kit.Should Be Fda / Ce / Dcgi Approved Measuring Device To Be Supplied , ( D ) Bedside Lipid Profile Measurement Kits.Reading Machine Should Be Provided , ( D ) Bedside Inr Measurement Kits.Reading Machine Should Be Provided , ( D ) Act Cartridges.Reading Machine Should Be Provided , Radiation Protection , ( D ) Vinyl Layered Lead Free Aprons Superior Quality Imported Types For Radiation Protection During Interventional Procedures. Covering Both Front And Backsingle Piece Medium Size.Should Be Fda / Ce / Dcgi Approved & Item To Be Demonstrated To Departmental Selection Committee , ( D ) Vinyl Layered Lead Free Aprons Superior Quality Imported Types For Radiation Protection During Interventional Procedures. Covering Both Front And Backsingle Piece Large Size.Should Be Fda / Ce / Dcgi Approved & Item To Be Demonstrated To The Departmental Selection Committee , ( D ) Vinyl Layered Lead Free Aprons Superior Quality Imported Types For Radiation Protection During Interventional Procedures. Covering Both Front And Backtwopiece Skirt And Blouse Type Medium Size. .Should Be Fda / Ce / Dcgi Approved & Item To Be Demonstrated To Departmental Selection Committee , ( D ) Vinyl Layered Lead Free Aprons Superior Quality Imported Types For Radiation Protection During Interventional Procedures. Covering Both Front And Backtwopiece Skirt And Blouse Type Large Size.Should Be Fda / Ce / Dcgi Approved & Item To Be Demonstrated To Departmental Selection Committee , ( D ) Vinyl Layered Lead Free Aprons Superior Quality Imported Types For Radiation Protection During Interventional Procedures. Covering Front Only Single Piece Small Size.Should Be Fda / Ce / Dcgi Approved & Item To Be Demonstrated To Departmental Selection Committee , ( D ) Vinyl Layered Lead Free Aprons Superior Quality Imported Types For Radiation Protection During Interventional Procedures. Covering Front Only Single Piece Medium Size.Should Be Fda / Ce / Dcgi Approved & Item To Be Demonstrated To Departmental Selection Committee , ( D ) Vinyl Layered Lead Free Aprons Superior Quality Imported Types For Radiation Protection During Interventional Procedures. Covering Front Only Single Piece Large Size.Should Be Fda / Ce / Dcgi Approved & Item To Be Demonstrated To Departmental Selection Committee , ( D ) Sterile Lead-Free Disposable Radiation Protection Shield.Should Be Fda / Ce / Dcgi Approved , ( D ) Soft Flexible Thyroid Collars Radiation Protection.Should Be Fda / Ce / Dcgi Approved & Item To Be Demonstrated To Departmental Selection Committee , ( D ) Gonadal Shields Radiation Protection.Should Be Fda / Ce / Dcgi Approved & Item To Be Demonstrated To Departmental Selection Committee , ( D ) Radaiation Protective Eye Goggles.Should Be Fda / Ce / Dcgi Approved & Item To Be Demonstrated To Departmental Selection Committee , ( D ) Radaiation Protective Head Gear.Should Be Fda / Ce / Dcgi Approved & Item To Be Demonstrated To Departmental Selection Committee , ( D ) Radiation Protection Drape Pads.Should Be Fda / Ce / Dcgi Approved , Electrophysiology , 5 French Fixed Curve Quadripolar Catheter With 2-5-2 Interelectrode Spacing. One Matching Connector For Every 5 Catheters.Should Be Fda / Ce / Dcgi Approved , 6 French Deflectable Quadripolar Catheter With 2-5-2 Interelectrode Spacing And Matching Connector.Should Be Fda / Ce / Dcgi Approved , 6 French Deflectable Decapolar Catheter With 2-5-2 Interelectrode Spacing And Matching Connector.Should Be Fda / Ce / Dcgi Approved , 4 Or 5 French Fixed Curve Decapolar Catheter With 2-5-2 Interelectrode For Coronary Sinus Placement. Should Be Fda / Ce / Dcgi Approved , 7 French Deflectable Duodecapolar Catheters With 2-5-2 Interelectrode Spacing With Matching Connectors.Should Be Fda / Ce / Dcgi Approved , 7 French Deflectable Duodecapolar Catheters With 2-8-2- ( 60 ) -2-8-2 Interelectrode Spacing With Matching Connectors.Should Be Fda / Ce / Dcgi Approved , 6 French Fixed Curve 20-Pole Catheter With 2-2-2 Spacing For Mapping In Crista Region , 20-Pole Variable Diameter Circular Mapping Catheter For Mapping In Pulmonary Veins , 7 French Quadripolar Radiofrequency Ablation Catheter With A 4 Mm Tip, Unidirectional Deflection, Availability In Small, Medium And Large Curves. Should Be Compatible With Stockert And Ibi Rf Generators And Suitable Connecting Cable Should Be Provided For Every 5 Catheters..Should Be Fda / Ce / Dcgi Approved , 7 French Quadripolar Radiofrequency Ablation Catheter With A 4 Mm Tip, Bidirectional Deflection, Availability In Small, Medium And Large Curves. Should Be Compatible With Stockert And Ibi Rf Generators And Suitable Connecting Cables Should Be Provided .Should Be Fda / Ce / Dcgi Approved , 7 French Quadripolar Radiofrequency Ablation Catheter With A 8 Mm Tip, Unidirectional Deflection, Availability In Medium And Large Curves. Should Be Compatible With Stockert And Ibi Rf Generators And Suitable Connecting Cable Should Be Provided For Every 5 Catheters..Should Be Fda / Ce / Dcgi Approved , 7 French Quadripolar Radiofrequency Ablation Catheter With A 8 Mm Tip, Bidirectional Deflection, Availability In Medium And Large Curves. Should Be Compatible With Stockert And Ibi Rf Generators And Suitable Connecting Cable Should Be Provided For Every 5 Catheters..Should Be Fda / Ce / Dcgi Approved , 7 French Quadripolar Radiofrequency Ablation Catheter With Irrigated Tip, Unidirectional Deflection And Availability In Medium And Large Curves. Should Be Compatible With Stockert And Ibi Rf Generators And Suitable Connecting Cable Should Be Provided For Every 5 Catheters. Tubing Set For Irrigation To Be Provided With Each Catheter.Should Be Fda / Ce / Dcgi Approved , 7 French Quadripolar Radiofrequency Ablation Catheter With Irrigated Tip, Bidirectional Deflection And Availability In Medium And Large Curves. Should Be Compatible With Stockert And Ibi Rf Generators And Suitable Connecting Cable Should Be Provided For Every 5 Catheters. Tubing Set For Irrigation To Be Provided With Each Catheter. Should Be Fda / Ce / Dcgi Approved , Quadripolar, Irrigated Tip, Radiofrequency Ablation Catheter With A 3.5 Mm Tip And Unidirectional Deflection For Use With The Carto Mapping System. Should Include Irrigation Tubing Set For Interface Between The Irrigation Pump And The Ablation Catheter And Matching External Reference Patch For Use With The Carto 3 System.Should Be Fda / Ce / Dcgi Approved , Quadripolar, Irrigated Tip, Radiofrequency Ablation Catheter With A 3.5 Mm Tip And Bidirectional Deflection For Use With The Carto Mapping System. Should Include Irrigation Tubing Set For Interface Between The Irrigation Pump And The Ablation Catheter And Matching External Reference Patch For Use With The Carto 3 System.Should Be Fda / Ce / Dcgi Approved , Quadripolar, Irrigated Tip, Radiofrequency Ablation Catheter With A 3.5 Mm Tip, Bidirectional Deflection And Contact Force Sensing For Use With The Carto Mapping System. Should Include Irrigation Tubing Set For Interface Between The Irrigation Pump And The Ablation Catheter And Matching External Reference Patch For Use With The Carto 3 System.Should Be Fda / Ce / Dcgi Approved , Multipolar Mapping Catheter For Use With The Carto Mapping System ( Pentaray Nav ) , Surface Electrode Kit For Use With The Ensite Navx System Including 3 Pairs Of Surface Patches, 10 Ecg Electrodes And 1 System Reference Electrode .Should Be Fda / Ce / Dcgi Approved , Multipolar Mapping Catheter Suitable For Omnipolar Mapping With The Ensite Navx System , Reusable Indifferent Electrode Pad Compatible With The Stockert Ablator.Should Be Fda / Ce / Dcgi Approved , Balloon Catheter For Cryoablation Of Pulmonary Veins With All Required Accessories Including Mapping Catheter And Steerable Sheath , Long Deflectable Sheath With Hemostatic Valve, Side Port, Atraumatic Tip, Braided Shaft, Uni- Or Bidirectional Steerability, Availability In Small, Medium Or Large Curves, Minimum Inner Diameter Or 7F, Minimum Length Of 65 Cms.Should Be Fda / Ce / Dcgi Approved , Steerable, Long Sheath Introducer Of At Least 8F Inner Diameter, With Atraumatic Tip And Bidirectional Steering, Designed For Use In Epicardial Mapping.Should Be Fda / Ce / Dcgi Approved , Implants Single Chamber , Ssir - Single Chamber Rate Responsive Implantable Multiprogrammable Pacemaker With Maximum Programmable Sensitivity Of 0.5 Mv Or More With Matching Leads And Subclavian Introducer Set To Be Quoted As One Set. Active Fixation Leads Should Be Supplied As Atrial ( 50% ) / Ventricular ( 50% ) . Should Be Fda / Ce / Dcgi Approved , Mri Ssir - Single Chamber Rate Responsible Implantable Multiprogrammable Mri Conditional Pacemaker With Matching Mri Conditional Atrial Or Ventricular Active Fixation Lead And Introducer Sheath Set. .Should Be Fda / Ce / Dcgi Approved , Implant Dual Chamber , Ddd - Dual Chamber Implantable Multiprogrammable Pacemaker With Shortest Programmable Av Delay Of 50 Ms, With Matching Set Of Steroid Eluting Active Fixation Atrial And Ventricular Leads And Two Matching Subclavian Introducers. Should Be Fda / Ce / Dcgi Approved , Dddr - Dual Chamber Rate-Responsive Implantable Multiprogrammable Pacemaker Withshortest Programmable Av Delay Of 50 Ms, With Matching Set Of Steroid Eluting Active Fixation Atrial And Ventricular Leads And Two Matching Subclavian Introducers. Should Be Fda / Ce / Dcgi Approved , Mri Dddr - Dual Chamber Mri Conditional Pacemaker With Matching Mri Conditional Atrial And Ventricular Active Fixation Leads And 2 Introducer Sheath Sets. Should Be Fda / Ce / Dcgi Approved , Aicd , Single Chamber, Single Coil Df4 Aicd - Single Chamber, Implantable Cardioverter Defibrillator For Treatment Of Life Threatening Ventricular Arrhythmias With Facility For Bradycardia Pacing And Tiered Therapy For Tachycardias, Maximum Shock Energy Of At Least 35 J, With Matching Single Coil, Integrated Bipolar Active Fixation Ventricular Leads. Should Be Fda / Ce / Dcgi Approved , Single Chamber, Dual Coil Df4 Aicd - Single Chamber, Implantable Cardioverter Defibrillator For Treatment Of Life Threatening Ventricular Arrhythmias With Facility For Bradycardia Pacing And Tiered Therapy For Tachycardias, Maximum Shock Energy Of At Least 35 J, With Matching Dual Coil, Integrated Bipolar Active Fixation Ventricular Leads..Should Be Fda / Ce / Dcgi Approved , Single Chamber, Single Coil Mri Conditional Df4 Aicd - Single Chamber, Mri Conditional Implantable Cardioverter Defibrillator For Treatment Of Life Threatening Ventricular Arrhythmias With Facility For Bradycardia Pacing And Tiered Therapy For Tachycardias, Maximum Shock Energy Of At Least 35 J, With Matching Single Coil, Integrated Bipolar Active Fixation Mri Conditional Ventricular Leads. Should Be Fda / Ce / Dcgi Approved , Dual Chamber Single Coil Df4 Aicd - Dual Chamber, Implantable Cardioverter Defibrillator For Treatment Of Life Threatening Ventricular Arrhythmias With Facility For Bradycardia Pacing And Tiered Therapy For Tachycardias, Maximum Shock Energy Of Atleast 35 J, With Matching Single Coil, Integrated Bipolar Active Fixation Atrial And Ventricular Leads..Should Be Fda / Ce / Dcgi Approved , Dual Chamber Dual Coil Df4 Aicd - Dual Chamber, Implantable Cardioverter Defibrillator For Treatment Of Life Threatening Ventricular Arrhythmias With Facility For Bradycardia Pacing And Tiered Therapy For Tachycardias, Maximum Shock Energy Of Atleast 35 J, With Matching Dual Coil, Integrated Bipolar Active Fixation Atrial And Ventricular Leads..Should Be Fda / Ce / Dcgi Approved , Dual Chamber Single Coil Mri Conditional Df4 Aicd - Dual Chamber, Mri Conditional Implantable Cardioverter Defibrillator For Treatment Of Life Threatening Ventricular Arrhythmias With Facility For Bradycardia Pacing And Tiered Therapy For Tachycardias, Maximum Shock Energy Of Atleast 35 J, With Matching Single Coil, Integrated Bipolar Active Fixation Mri Conditional Atrial And Ventricular Leads..Should Be Fda / Ce / Dcgi Approved , Single Chamber Subcutaneous Icd With Lead Designed For Subcutaneous Placement, Introducer And Other Accessories , Crt-P & D , Crt-P-Triple Chamber Pacing System Comprising Pacemaker, Active Fixation Atrial, Active Fixation Rv Leads And Passive Bipolar Over The Wire Coronary Sinus Lead ( Lv Lead ) . Should Include Compatible Short Sheaths With Valve, Long Preshaped Slittable Sheaths For Coronary Sinus Cannulation In Multiple Shapes, Subselective Inner Sheaths, Guidewire And Occlusion Balloon Catheter For Coronary Venography. Coronary Sinus Lead Should Be Available In Multiple Curves / Sizes..Should Be Fda / Ce / Dcgi Approved , Crt-P-Triple Chamber Pacing System Comprising Pacemaker, Active Fixation Atrial, Active Fixation Rv Leads And Passive Quadripolar Over The Wire Coronary Sinus Lead ( Lv Lead ) . Should Include Compatible Short Sheaths With Valve, Long Preshaped Slittable Sheaths For Coronary Sinus Cannulation In Multiple Shapes, Subselective Inner Sheaths, Guidewire And Occlusion Balloon Catheter For Coronary Venography. Coronary Sinus Lead Should Be Available In Multiple Curves / Sizes..Should Be Fda / Ce / Dcgi Approved , Crt-P-Triple Chamber Pacing System Comprising Pacemaker, Active Fixation Atrial, Active Fixation Rv Leads And Active Fixation Quadripolar Over The Wire Coronary Sinus Lead ( Lv Lead ) Specifically With Built In Screw In Type Of Mechanism For Maintaining Stable Position. Should Include Compatible Short Sheaths With Valve, Long Preshaped Slittable Sheaths For Coronary Sinus Cannulation In Multiple Shapes, Subselective Inner Sheaths, Guidewire And Occlusion Balloon Catheter For Coronary Venography. Coronary Sinus Lead Should Be Available In Multiple Curves / Sizes..Should Be Fda / Ce / Dcgi Approved , Mri Crt-P-Triple Chamber Pacing System Comprising Mri Conditional Pacemaker, Active Fixation Mri Conditional Atrial, Active Fixation Mri Conditional Rv Leads And Passive Quadripolar Over The Wire Mri Conditional Coronary Sinus Lead ( Lv Lead ) . Should Include Compatible Short Sheaths With Valve, Long Preshaped Slittable Sheaths For Coronary Sinus Cannulation In Multiple Shapes, Subselective Inner Sheaths, Guidewire And Occlusion Balloon Catheter For Coronary Venography. Coronary Sinus Lead Should Be Available In Multiple Curves / Sizes..Should Be Fda / Ce / Dcgi Approved , Mri Crt-P-Triple Chamber Pacing System Comprising Mri Conditional Pacemaker, Mri Conditional Active Fixation Atrial, Mri Conditional Active Fixation Rv Leads And Mri Conditional Active Fixation Quadripolar Over The Wire Coronary Sinus Lead ( Lv Lead ) Specifically With Built In Screw In Type Of Mechanism For Maintaining Stable Position. Should Include Compatible Short Sheaths With Valve, Long Preshaped Slittable Sheaths For Coronary Sinus Cannulation In Multiple Shapes, Subselective Inner Sheaths, Guidewire And Occlusion Balloon Catheter For Coronary Venography. Coronary Sinus Lead Should Be Available In Multiple Curves / Sizes..Should Be Fda / Ce / Dcgi Approved , Single Coil Df-4 Crt-D - Triple Chamber Pacemaker System With Cardioverter Defibrillator For Treatment Of Life Threatening Ventricular Arrhythmias With Facility For Crt Pacing And Tiered Therapy For Tachycardias, Maximum Shock Energy Of Atleast 35 J Comprising Active Fixation Atrial Lead, Single Coil With Integrated Bipolar Active Fixation Rv Lead And Passive Quadripolar Over The Wire Coronary Sinus Lead ( Lv Lead ) . Should Include Compatible Short Sheaths With Valve, Long Preshaped Slittable Sheaths For Coronary Sinus Cannulation In Multiple Shapes, Subselective Inner Sheaths, Guidewire And Occlusion Balloon Catheter For Coronary Venography. Coronary Sinus Lead Should Be Available In Multiple Curves / Sizes.Should Be Fda / Ce / Dcgi Approved , Single Coil Df-4 Crt-D - Triple Chamber Pacemaker System With Cardioverter Defibrillator For Treatment Of Life Threatening Ventricular Arrhythmias With Facility For Crt Pacing And Tiered Therapy For Tachycardias, Maximum Shock Energy Of Atleast 35 J Comprising Active Fixation Atrial Lead, Single Coil With Integrated Bipolar Active Fixation Ventricular Rv Lead And Active Fixation Quadripolar Over The Wire Coronary Sinus Lead ( Lv Lead ) Specifically With Built In Screw In Type Of Mechanism For Maintaining Stable Position.Should Include Compatible Short Sheaths With Valve, Long Preshaped Slittable Sheaths For Coronary Sinus Cannulation In Multiple Shapes, Subselective Inner Sheaths, Guidewire And Occlusion Balloon Catheter For Coronary Venography. Coronary Sinus Lead Should Be Available In Multiple Curves / Sizes.Should Be Fda / Ce / Dcgi Approved , Mri Conditional Single Coil Df-4 Crt-D - Triple Chamber Mri Conditional Pacemaker System With Cardioverter Defibrillator For Treatment Of Life Threatening Ventricular Arrhythmias With Facility For Crt Pacing And Tiered Therapy For Tachycardias, Maximum Shock Energy Of Atleast 35 J Comprising Active Fixation Mri Conditional Atrial Lead, Single Coil With Integrated Bipolar Active Fixation Mri Conditional Rv Lead And Passive Quadripolar Over The Wire Mri Conditional Coronary Sinus Lead ( Lv Lead ) . Should Include Compatible Short Sheaths With Valve, Long Preshaped Slittable Sheaths For Coronary Sinus Cannulation In Multiple Shapes, Subselective Inner Sheaths, Guidewire And Occlusion Balloon Catheter For Coronary Venography. Coronary Sinus Lead Should Be Available In Multiple Curves / Sizes.Should Be Fda / Ce / Dcgi Approved , Mri Conditional Single Coil Df-4 Crt-D - Triple Chamber Pacemaker System With Cardioverter Defibrillator For Treatment Of Life Threatening Ventricular Arrhythmias With Facility For Crt Pacing And Tiered Therapy For Tachycardias, Maximum Shock Energy Of Atleast 35 J Comprising Active Fixation Mri Conditional Atrial Lead, Single Coil With Integrated Bipolar Active Fixation Mri Conditional Rv Lead And Active Fixation Quadripolar Over The Wire Mri Conditional Coronary Sinus Lead ( Lv Lead ) Specifically With Built In Screw In Type Of Mechanism For Maintaining Stable Position.Should Include Compatible Short Sheaths With Valve, Long Preshaped Slittable Sheaths For Coronary Sinus Cannulation In Multiple Shapes, Subselective Inner Sheaths, Guidewire And Occlusion Balloon Catheter For Coronary Venography. Coronary Sinus Lead Should Be Available In Multiple Curves / Sizes.Should Be Fda / Ce / Dcgi Approved , Conduction System Pacing , Single Chamber Ssir For Conduction System Pacing-Single Chamber Rate Responsive Implantable Multiprogrammable Pacemaker With Lead And Specialised Long Sheath Designed For Conduction System Pacing, Compatible Short Sheaths With Valve And Other Accessories Required For Conduction System Pacing. Should Be Fda / Ce / Dcgi Approved. , Mri Conditional Single Chamber Ssir For Conduction System Pacing-Single Chamber Rate Responsive Implantable Multiprogrammable Pacemaker With Lead And Specialised Long Sheath Designed For Conduction System Pacing, Compatible Short Sheaths With Valve And Other Accessories Required For Conduction System Pacing. Should Be Fda / Ce / Dcgi Approved. , Mri Conditional Dual Chamber Dddr For Conduction System Pacing-Dual Chamber Rate-Responsive Implantable Multiprogrammable Mri Conditional Pacemakerwith Active Fixation Mri Conditional Atrial Lead, Lead With Specialised Long Sheath Designed For Conduction System Pacing, Compatible Short Sheaths With Valve And Other Accessories For Conduction System Pacing. Should Be Fda / Ce / Dcgi Approved , Conduction System Pacing Optimised Crt-P-Triple Chamber Pacing System Comprising Pacemaker, Active Fixation Atrial Lead, Quadripolar Coronary Sinus Lead, Lead With Specialised Long Sheath Designed For Condution System Pacing. Should Include Long Preshaped Slittable Sheaths For Coronary Sinus Cannulation In Multiple Shapes, Subselective Inner Sheaths, Guidewire, Occlusion Balloon Catheter For Coronary Venography, Compatible Short Sheaths With Valve And Sheath Slitters. Coronary Sinus Lead Should Be Available In Multiple Curves / Sizes. Should Be Fda / Ce / Dcgi Approved , Mri Conditional Conduction System Pacing Optimised Crt-P-Triple Chamber Pacing System Comprising Mri Conditional Pacemaker, Active Fixation Mri Conditional Atrial Lead, Quadripolar Mri Conditonal Coronary Sinus Lead, Lead With Specialised Long Sheath Designed For Condution System Pacing. Should Include Long Preshaped Slittable Sheaths For Coronary Sinus Cannulation In Multiple Shapes, Subselective Inner Sheaths, Guidewire, Occlusion Balloon Catheter For Coronary Venography, Compatible Short Sheaths With Valve And Sheath Slitters. Coronary Sinus Lead Should Be Available In Multiple Curves / Sizes. Should Be Fda / Ce / Dcgi Approved , Mri Conditional Conduction System Pacing Optimised Crt-P-Triple Chamber Pacing System Comprising Mri Conditional Pacemaker, Active Fixation Mri Conditional Atrial Lead, Active Fixation & Screw In Type Of Quadripolar Mri Conditional Coronary Sinus Lead ( Lv Lead ) , Mri Conditional Lead With Specialised Long Sheath Designed For Condution System Pacing. Should Include Long Preshaped Slittable Sheaths For Coronary Sinus Cannulation In Multiple Shapes, Subselective Inner Sheaths, Guidewire, Occlusion Balloon Catheter For Coronary Venography, Compatible Short Sheaths With Valve And Sheath Slitters. Coronary Sinus Lead Should Be Available In Multiple Curves / Sizes. Should Be Fda / Ce / Dcgi Approved , Pacing Leads , Steroid Eluting Bipolar Active Fixation Atrial Leads With Introducer Sheath.Should Be Fda / Ce / Dcgi Approved , Steroid Eluting Bipolar Active Fixation Ventricular Leads With Introducer Sheath.Should Be Fda / Ce / Dcgi Approved , Single And Dual Coil ( 50-50% ) , Integrated Bipolar Active Fixation Df4 Type Icd Leads.Should Be Fda / Ce / Dcgi Approved , Quadripolar Lead Specially Designed For Placement In Coronary Sinus For Lv Pacing. Should Be Supplied With 9F Short Sheath With Valve, Long Preshaped Slittable Sheaths In Variousshapes For Cs Cannulation And Inner Subselective Sheath. Lead, Long Sheath, Subselective Sheath And Short Sheath Should Be Quoted As One Set. Should Be Fda / Ce / Dcgi Approved , Quadripolar Lead Specially Designed For Placement In Coronary Sinus For Lv Pacing With Built In Screw In Type Of Active Fixation Mechanism For Maintaining Stable Position. Should Be Supplied With Compatible Short Sheath With Valve, Long Preshaped Slittable Sheaths In Various Shapes For Cs Cannulation And Inner Subselective Sheath. Lead, Long Sheath, Subselective Sheath And Short Sheath Should Be Quoted As One Set. Should Be Fda / Ce / Dcgi Approved , Lumenless Lead With Preshaped Sheath ( Specifically Designed For Conduction System Pacing ) Along With Slitter And Short Subclavian Sheath As One Set. , Stylet Driven Ventricular Lead For Conduction System Pacing With Sheath And Other Compatible Accessories. , Unipolar Epicardial Pacing Leads , Bipolar Epicardial Pacing Leads , Leadless Pacemaker , Miniaturised Pacemaker For Use As Leadless Pacemaker With Delivery System And Other Required Accessories , Temporary Pacing , ( S ) Temporary Pacing Leads Sizes With 5F / 6F.Should Be Fda / Ce / Dcgi Approved , ( S ) Balloon Flow Assisted Temporary Pacing Lead ( 5F And 6F .Should Be Fda / Ce / Dcgi Approved , ( D ) Single Chamber Demand Cum Overdrive Temporary Pulse Generators With Various Dual Chamber And Single Chamber Modes, Capable Of Overdrive Pacing.Should Be Fda / Ce / Dcgi Approved , ( D ) Dual Chamber Demand Cum Overdrive Temporary Pulse Generators Withvarious Dual Chamber And Single Chamber Modes, Capable Of Overdrive Pacing.Should Be Fda / Ce / Dcgi Approved , Loop Recorders / Remote Monitoring , ( D ) Implantable Loop Recorder - Long Term ( Ilr ) For Subcutaneous Implantation, Capable Of Recording At Least One Channel Subcutaneous Ecg. Matching Hand-Held Activator Should Be Provided. .Should Be Fda / Ce / Dcgi Approved , ( D ) External Disposableexternal Loop Recorder With Capability To Record At Least One Ecg Lead For A Period Of At Least 7 Days. Recording Patch / Electrodes Should Be Water Resistant Allowing Patient To Bathe. Episodes Should Be Identified Automatically And It Should Also Be Possible To Record Patient Triggered Episodes. Transmission Should Be Wireless And Monitored In A 24X7 Staffed Monitoring Center. Quoted Cost Should Include Disposable Electrode Set, Recorder, Hand-Held Activator, Data Transmission And Reporting For The Period Of Recording..Should Be Fda / Ce / Dcgi Approved , ( D ) Wrist Wearable, Reusable Recorder Capable Of Remote Monitoring Of Physical Activity By Step Count And Physical Inactivity, Heart Rate, Spo2, And Sleep, With Rechargeable Battery Lasting At Least 72 Hours Between Charges Compatible With Android Os. Waterproof With A Year Warranty. , ( D ) Wrist Wearable, Reusable Recorder Capable Of Remote Monitoring Of Physical Activity By Step Count And Physical Inactivity, Heart Rate, Spo2, And Sleep, With Rechargeable Battery Lasting At Least 72 Hours Between Charges Compatible With Ios . Waterproof With A Year Warranty. , ( D ) Wrist Wearable, Reusable Rechargable Recorder Capable Of Remote Monitoring Of Physical Activity By Step Count And Physical Inactivity, Heart Rate, Spo2, And Sleep, With Rechargeable Battery Lasting At Least 72 Hours Between Charges Compatible With Both Android And Ios . Waterproof With A Year Warranty. , ( D ) Medical Grade Reusable Rechargeable Monitoring Wrist Wearable Device For Remote Monitoring Of Continuous Pulse Rate, Physical Activity, Respiration Rate And Patient Triggered Ecg And Spo2. Automated Arrhythmia Warning On Ppg And Automated Arrhythmia Diagnosis On Ecg. Remote Recording Of Ppg And Ecg Waveforms Should Be Possible. Battery Life Should Be A Minimum 48 Hours And Waterproof Atip67 Or Above. Patient Data Should Be Visible To The Patient Via An Android Or Ios Smartphone And To The Physician Via A Web Interphase. The Unit Should Be Cdsco Certified And Us Fda Approved For Ppg-Based Arrhythmia And Ecg Arrhythmia Diagnosis And If Not Human Clinical Trial Data Indicating A Specificty And Sensitivity Of 95% Or Above Should Be Submitted. The Unit Should Have 3-Year Warranty. , Surgical Instruments , ( D ) One Set Of High Grade Stainless Steel Surgical Instruments For Minor Surgical Procedure. Must Include The Following Instruments – Sponge Forceps 2 Nos, Towel Clamp – 4, Hemostatic Crile Forceps Straight – 4, Hemostatic Crile Forceps Curved – 6, Allis Tissue Forceps – 2, Mayo Hegar Needle Holder 6 Inches – 1, Mayo Hegar Needle Holder 7 Inches – 1, Mayo Scissors Straight – 1, Metzenbaum Scissors Curved – 1, Small Curved Scissors – 1, Small Straight Scissors – 1, Thumb Forceps – 2, Adsons Toothed Forceps – 2, Knife Handle #7 – 1, Knife Handle #4 – 1, Weitlaner Self Retaining Retractor Sharp 5 Inches – 1, Double Hook Retractor – 2, Right Angle Forceps – 1.Should Be Fda / Ce / Dcgi Approved & Item To Be Demonstrated To Departmental Selection Committee , Lead Extraction , ( D ) Lead Locking Device For Transvenous Extraction Of Chronically Implanted Pacemaker And Defibrillator Leads With Mechanical Rotating Dilator 9F / 11F / 13F Diameter With A Flexible Shaft And Dilator Sheath Set .Should Be Fda / Ce / Dcgi Approved , ( D ) Lead Locking Device For Extraction Of Chronically Implanted Leads , Monitor / Ecg / Tmt / Defibrillator Consumables , ( S ) Spo2 Probe Compaitable With Monitor Model : Space Labs.Should Be Fda / Ce / Dcgi Approved , ( S ) Ecg Probe Compaitable With Monitor Model : Space Labs.Should Be Fda / Ce / Dcgi Approved , ( S ) Bp Cuff Compaitable With Monitor Model : Space Labs.Should Be Fda / Ce / Dcgi Approved , ( S ) Spo2 Probe Compaitable With Monitor Model : Philips Mp 30.Should Be Fda / Ce / Dcgi Approved , ( S ) Ecg Leads Compaitable With Monitor Model : Philips Mp 30.Should Be Fda / Ce / Dcgi Approved , ( S ) Nibp Cuff ( Adult ) Compaitable With Monitor Model : Philips Mp 30.Should Be Fda / Ce / Dcgi Approved , ( S ) Nibp Cuff ( Paediatrics ) Compaitable With Monitor Model : Philips Mp 30.Should Be Fda / Ce / Dcgi Approved , ( S ) Bp Cuff ( Adult ) Compaitable With Monitor Model : Philips Mp 30.Should Be Fda / Ce / Dcgi Approved , ( S ) Bp Cuff ( Paediatrics ) Compaitable With Monitor Model : Philips Mp 30.Should Be Fda / Ce / Dcgi Approved , ( S ) Arterial Pressure Monitoring Transducers ( Disposable ) .Should Be Fda / Ce / Dcgi Approved , ( S ) Syringe For Pressure Injector ( Disposable ) - Liebel Flarsheim Injector 100Ml.Should Be Fda / Ce / Dcgi Approved , ( S ) Spo2 Probe Disposable Compaitable With Multi Purpose Monitor Philips A3.Should Be Fda / Ce / Dcgi Approved , ( S ) Ecg Cable Compaitable With Multi Purpose Monitor Philips A3.Should Be Fda / Ce / Dcgi Approved , ( S ) Nibp Cuff ( Adult ) Compaitable With Multi Purpose Monitor Philips A3.Should Be Fda / Ce / Dcgi Approved , ( S ) Nibp Cuff ( Child ) Compaitable With Multi Purpose Monitor Philips A3.Should Be Fda / Ce / Dcgi Approved , ( S ) Spo2 Probe Disposable Compaitable With Multi Purpose Monitor Agilent.Should Be Fda / Ce / Dcgi Approved , ( S ) Ecg Cable Compaitable With Multi Purpose Monitor Agilent.Should Be Fda / Ce / Dcgi Approved , ( S ) Nibp Cuff ( Adult ) Compaitable With Multi Purpose Monitor Agilent.Should Be Fda / Ce / Dcgi Approved , ( S ) Nibp Cuff ( Child ) Compaitable With Multi Purpose Monitor Agilent.Should Be Fda / Ce / Dcgi Approved , ( S ) Spo2 Probe Disposable Compaitable With Multi Purpose Monitor Mec 1200.Should Be Fda / Ce / Dcgi Approved , ( S ) Ecg Cable Compaitable With Multi Purpose Monitor Mec 1200.Should Be Fda / Ce / Dcgi Approved , ( S ) Nibp Cuff ( Adult ) Compaitable With Multi Purpose Monitor Mec 1200.Should Be Fda / Ce / Dcgi Approved , ( S ) Nibp Cuff ( Child ) Compaitable With Multi Purpose Monitor Mec 1200.Should Be Fda / Ce / Dcgi Approved , ( S ) Superior Quality Ecg Jelly In Bottles Of 250 G Long Lasting .Should Be Fda / Ce / Dcgi Approved , ( S ) Superior Quality Ecg Echo Jelly In Bottles Of 250 G Long Lasting .Should Be Fda / Ce / Dcgi Approved , ( S ) Mortara Eli-250 Machinecable.Should Be Fda / Ce / Dcgi Approved , ( S ) Mortara Eli 350 Machinecable.Should Be Fda / Ce / Dcgi Approved , ( S ) Chest Bulbs Adult.Should Be Fda / Ce / Dcgi Approved , ( S ) Chest Bulbs Pediatrics.Should Be Fda / Ce / Dcgi Approved , ( S ) Limb Leads Adult.Should Be Fda / Ce / Dcgi Approved , ( S ) Limb Leads Pediatrics.Should Be Fda / Ce / Dcgi Approved , ( S ) Biocare Ecg Recorder Paper.Should Be Fda / Ce / Dcgi Approved , ( S ) Biocare Ecg Cable.Should Be Fda / Ce / Dcgi Approved , ( S ) Mortara Eli-250 Ecg Recorder Head.Should Be Fda / Ce / Dcgi Approved , ( S ) Mortara Eli-350 Ecg Recorder Head.Should Be Fda / Ce / Dcgi Approved , ( S ) Mortara Eli-350 Ecg Paper..Should Be Fda / Ce / Dcgi Approved , ( S ) Mortara Eli-250 Ecg Paper..Should Be Fda / Ce / Dcgi Approved , ( S ) Edan Multichannel Machine Paper.Should Be Fda / Ce / Dcgi Approved , ( S ) Nihon Koden Multichannel Machine Paper Roll Type.Should Be Fda / Ce / Dcgi Approved , ( S ) Mortara Tmt Paper.Should Be Fda / Ce / Dcgi Approved , ( S ) Ag / Agcl Imported Patient Prejelled Electrodes For Long-Term Monitoring Superior Quality .Should Be Fda / Ce / Dcgi Approved , ( D ) Disposable Heartstart Adult Plus Mutifunction Defibrillation Pads For Use With The Philips Defibrillator.Should Be Fda / Ce / Dcgi Approved , ( D ) Disposable Pads For Defibrillation / Transcutaneous Pacing For Use With The Zoll Defibrillator.Should Be Fda / Ce / Dcgi Approved , ( D ) Disposable Pads For Defibrillation For Use With The Zoll Aed.Should Be Fda / Ce / Dcgi Approved , ( D ) Reusable Pads For Defibrillation For Use With The Zoll Aed.Should Be Fda / Ce / Dcgi Approved , Ventilator Consumables , ( S ) Patient Tubing System Compatible With Maquet S Ventilator.Should Be Fda / Ce / Dcgi Approved , Test Kits , ( S ) Spot Test Kits For Hiv .Should Be Fda / Ce / Dcgi Approved , ( S ) Spot Test Kits For Hbsag .Should Be Fda / Ce / Dcgi Approved , ( S ) Spot Test Kits For Hcv .Should Be Fda / Ce / Dcgi Approved , Cleaning / Cutting Disposables , ( S ) Stickymats / Tacky Mats 1 To 30 On 30 Peel Tags, Anti Ststic, With Holding Stick Time : > 1000 Mins, Price Per Box To Be Quoted With Number Of Units Per Box.Should Be Fda / Ce / Dcgi Approved , Surgical Hair Clipper ( General Blade ) - Cleaning Regular Area Battery Operated For Pre-Operative Preparational.Hair Removal From Body With No Risk Of Cuts On The Skin.To Be Supplied With Suitable Charger And Blade.Hair Clipper Machine Should Be Used In Wet Or Dry Condition And Recharger For The Machine Should Be Provided. ( One Machine For 400 Hair Clipping Blades ) , Surgical Hair Clipper ( Sensitive Blade ) - Cleaning Sensitivearea Battery Operated For Pre-Operative Preparational.Hair Removal From Body With No Risk Of Cuts On The Skin.To Be Supplied With Suitable Charger And Blade.Hair Clipper Machine Should Be Used In Wet Or Dry Condition And Recharger For The Machine Should Be Provided. ( One Machine For 400 Hair Clipping Blades ) , Drapes / Covers / Packing / Store Disposable , ( S ) Disposable Sterile Drapes For Coronary Angiography / Angioplasty Compatible With Bilateral Femoral And Radial Approaches With Absorbable Material.Sample To Be Supplied For Testing , ( S ) Disposable Sterile Drapes For Permanent Pacemaker Implantationl And R Pectoral Approaches.Sample To Be Supplied For Testing , ( S ) Tissue Paperbaseddisposable Bed Covers In Continious Rolls Of Width 90Cm For Use On Trolleys & Cardiac Cath Lab Tables..Sample To Be Supplied For Testing , ( S ) Disposable Sterile Angioplasty Drapes Kits Witha. One Unit -Drape Angioplasty Compatible With Bilateral Femoral And Radial Approaches With Absorbable Material B. Three Unitsdisposable Sterile Gowns C. One Unit Disosable Centre Hole Towel D. One Unit Cath Trolleydrape.Sample To Be Supplied For Testing , ( S ) Disposable Gown & Pyjama Set For Cath Lab Procedure In Dark Colours - Brown / Dark Blue / ( Small / Medium / Large ) .Sample To Be Supplied For Testing , ( D ) Small Size Packing Material Compatible With Automated Sealing Machine For Eto Sterilization Of Consumables..Item To Be Demonstrated To Departmental Selection Committee. , ( D ) Intermediate Size Packing Material Compatible With Automated Sealing Machine For Eto Sterilization Of Consumables..Item To Be Demonstrated To Departmental Selection Committee. , ( D ) Large Size Packing Material Compatible With Automated Sealing Machine For Eto Sterilization Of Consumables..Item To Be Demonstrated To Departmental Selection Committee. , ( S ) Disposable, Sterile Cover For Fluoroscopy System Image Intensifier. Should Fit Image Intensifier Of Different Sizes And Should Have Elastic Band For Easy Retention..Should Be Fda / Ce / Dcgi Approved & Item To Be Demonstrated To Departmental Selection Committee , ( S ) Disposable, Sterile Cover For Fluoroscopy System Radiation Shield. Should Fit Image Intensifier Of Different Sizes And Should Have Elastic Band For Easy Retention..Should Be Fda / Ce / Dcgi Approved & Item To Be Demonstrated To Departmental Selection Committee , ( D ) Disposable Sterile Ultrasound Probe Cum Cable Long Cover Made Of Polyethene Or Similar Translucent Material With A Flat End. A Small Pouch Of Sterile Ultrasound Jelly, Elastic Bands And Or Paper Adhesive Bands For Binding The Probe And Cable To Be Provided As A Sterile Set. Different Sizes That Are Compatible With Adult And Pediatric Cardiac / Vascular / Abdominal Probes To Be Supplied. , ( D ) Reuasable Cath-Lab Cotton Dress Shirt With Three Pockets And Pyjama With Two Pockets Large And Medium Sized Light Blue Colour With The Label Of “ Cath-Lab Jipmer” On Both The Shirt And The Pyjama And Size Printed.Sample To Be Supplied , ( S ) Disposable Cath-Lab Gowns Light Blue Colour Full Size And Elastic Wrist Bands With Water / Blood Impenetrable Front And Hand Shielding.Should Be Fda / Ce / Dcgi Approved , ( S ) Disposable Paper-Based Sterile Front Buttoned Black / Brown / Dark Blue Half Sleeve Shirt And Pyjama For Cath Lab Patient Dress.Small, Medium, Large Sizes Should Be Fda / Ce / Dcgi Approved , ( S ) Compact Disk- Recordable ( Cd-R ) With Hard Shell Box.Sample To Be Submitted To Departmental Selection Committee. , ( S ) Dvd- Recordable ( Dvd-R ) With Hard Shell Box.Item To Be Demonstrated To Departmental Selection Committee. , ( S ) Cd Sticker Labels With Department Of Cardiology , Jipmer Stickers, With Space For Printing Angio No And Cd No.Item To Be Demonstrated And Discussedto Departmental Selection Committee. , ( S ) Permanent Marker Pens- Thin Script- Black.Sampleto Be Submittedto Departmental Selection Committee. , ( S ) White Board Markers Black And Blue.Sampleto Be Submittedto Departmental Selection Committee. , ( D ) Washable And Autoclavable Cut Shoes ( Clogs ) Specially Designed For Wearing In Cathlabs / Operation Rooms / Icus Wear Slippers At Least 12 Inch Foot Length. ( Roomy Fit ) . Should Have Non Collapsible Sole To Support The Arch Of Foot. The Brochure Mentioning The Details Of The Product Should Be Submitted . Mention Various Sizes Available. ( Small, Medium, Large And Extra Large ) .Item To Be Demonstrated To The Departmental Selection Committee , Monitoring Devices - Non Consumables , ( D ) Battery Operated Automated Digital Bp Apparatus With Adult, Large Adult And Pediatric Cuffs With 3 Yr Warranty.Item To Be Demonstrated To Departmental Selection Committee. , ( D ) Digital Bp Apparatus Heavy Duty, With Adult, Large Adult And Pediatric Cuffs Running In Ac Power With Rechargable Lithium Ion Batters For Use In Opd And Ward With 3 Yr Warranty.Item To Be Demonstrated To Departmental Selection Committee. , ( D ) Digital Bp, Spo2, Respiratory Rate, Temperaturemeasuring Apparatus Heavy Duty, With Adult, Large Adult And Pediatric Cuffs Running In Ac Power With Rechargeable Lithium-Ion Battery For Use In Opd And Ward3 Yr Warranty.Item To Be Demonstrated To The Departmental Selection Committee. , ( D ) Digital Automated Bp Apparatus For Use With Tmt Machine With Automatic Noise Detection And Artefact Cancellation And Ability For Ecg Gating , ( D ) Digital Weighing Scale For Patient Weight With 3 Yr Warranty.Item To Be Demonstrated To Departmental Selection Committee. , ( D ) Battery Operated Pocket Sized Spo2 Probes.Item To Be Demonstrated To Departmental Selection Committee. , ( D ) Digital Stadiometer For Height Measurement. , ( D ) Temperature And Humidity Monitors For Cathlabs And Icu. Should Have Maximum And Minimum Values For 24 Hours On Display And Ability To Store 30 Days Data For Export. , ( D ) Dual Zone Temperature Monitors For Refrigerators For Monitoring Freezer And Cabin Temperatures. Should Have Maximum And Minimum Values For 24 Hours On Display And Ability To Store 30 Days Data For Export. , ( D ) Multiparameter Monitors Ecg, Spo2, Nibp With 3Yr Warrranty And2 Sets Of Cables.Item To Be Demonstrated To The Departmental Selection Committee. , ( D ) Syringe Infusion Pumps With 3 Yr Warranty.Item To Be Demonstrated To Departmental Selection Committee. , ( D ) Ot Light- Floor Mounted, Led Source , Brightness And Focus Adjustable With 3 Yr Warranty.Item To Be Demonstrated To Departmental Selection Committee.
Corrigendum
| Sr No | Corrigendum Date | Corrigendum | Type | New Submission Date |
|---|---|---|---|---|
| 1 | 03-Apr-2024 | Date Extension | Date | 11-Apr-2024 |
BOQ
| Sl. No. | Item Description |
| 1 | IMPORTANT CONDITIONS FOR CARDIOLOGY TENDER: Abbreviations and additional conditions 1. S-ITEMS WITH (Prefix \"S\") sample MUST be submitted to the department with item number and name superscribed within 15 days of online tender opening, 2. EX-Patient Size Variable Implantable Devices and Consumables (Prefix EX) (Stents/ASD/VSD/PDA/Balloons/Coils/ etc- the supplier should maintain a stock of all the sizes in the matrix in the cath labs so as to exchange the items suitable for an individual patient till the last item is used. 3. D- ITEMS WHICH HAS A PREFIX (D) has to be demonstrated by the vendor to the departmental selection committee on the date of technical evaluation informed by email only 4. All implantable devices should be Licensed for sale in India by DCGI/CDSCO and should be USFDA approved, failing which Human Clinical Trial RCT data Published in Indexed Journals should be submitted 5. All implantable devices should be supplied only by companies that have supplied to major hospitals(500 beds) in India or abroad (proof to be enclosed) 6. Items supplied should have an expiration date of more than 12 months from the date of supply. 7. For some items like BMV ballons and ASD/VSD/PDA devices, cables and accessories shall be bought from the same company selected as L1 in the category of Device only item8. For all items, a detailed technical brochure in pdf format and approvals, certifications, etc have to be sent to the department stores within 10 days of online tender opening to [email protected] with the subject as the TenderNo/Serial No/item name/manufacturer name/brand name 9. While mentioning the Make/Model of consumable /implant/non-consumable, please mention the manufacturer name AND model name Model number 10.Non-compliance of all the above clauses will lead to the rejection of the item1. FEMORAL ACCESS |
| 2 | (S) FEMORALSHEATH SYSTEMS SIZE 4F 7.5 cm with accessories for insertion.Should be FDA\"/CE\"/DCGI approved |
| 3 | (S) FEMORALSHEATH SYSTEMS SIZE 4F 11 cm with accessories for insertion.Should be FDA\"/CE\"/DCGI approved |
| 4 | (S) FEMORAL SHEATH SYSTEMS SIZES 5F 7.5 cm with accessories for insertion.Should be FDA\"/CE\"/DCGI approved |
| 5 | (S) FEMORAL SHEATH SYSTEMS SIZES 5F 11 cm with accessories for insertion.Should be FDA\"/CE\"/DCGI approved |
| 6 | (S) FEMORAL SHEATH SYSTEMS SIZES 6F 7.5 cm with accessories for insertion.Should be FDA\"/CE\"/DCGI approved |
| 7 | (S) FEMORAL SHEATH SYSTEMS SIZES 6F 11 cm with accessories for insertion.Should be FDA\"/CE\"/DCGI approved |
| 8 | (S) FEMORAL SHEATH SYSTEMS SIZES 7F 7.5 cm with accessories for insertion.Should be FDA\"/CE\"/DCGI approved |
| 9 | (S) FEMORAL SHEATH SYSTEMS SIZES 7F 11 cm with accessories for insertion.Should be FDA\"/CE\"/DCGI approved |
| 10 | (S) FEMORAL SHEATH SYSTEMS SIZES 8F 7.5 cm with accessories for insertion.Should be FDA\"/CE\"/DCGI approved |
| 11 | (S) FEMORAL SHEATH SYSTEMS SIZES 8F 11 cm with accessories for insertion.Should be FDA\"/CE\"/DCGI approved |
| 12 | (S) FEMORAL SHEATH SYSTEMS SIZES 9F 7.5 cm with accessories for insertion.Should be FDA\"/CE\"/DCGI approved |
| 13 | (S) FEMORAL SHEATH SYSTEMS SIZES 9F 11 cm with accessories for insertion.Should be FDA\"/CE\"/DCGI approved |
| 14 | (S) FEMORAL SHEATH SYSTEMS SIZES 10F 7.5 cm with accessories for insertion.Should be FDA\"/CE\"/DCGI approved |
| 15 | (S) FEMORAL SHEATH SYSTEMS SIZES 10F 11 cm with accessories for insertion.Should be FDA\"/CE\"/DCGI approved |
| 16 | (S) FEMORAL SHEATH SYSTEMS SIZES 11F 7.5 cm with accessories for insertion.Should be FDA\"/CE\"/DCGI approved |
| 17 | (S) FEMORAL SHEATH SYSTEMS SIZES 11F 11 cm with accessories for insertion.Should be FDA\"/CE\"/DCGI approved |
| 18 | (S) FEMORAL SHEATH SYSTEMS SIZES 12F 7.5 cm with accessories for insertion.Should be FDA\"/CE\"/DCGI approved |
| 19 | (S) FEMORAL SHEATH SYSTEMS SIZES 12F 11 cm with accessories for insertion.Should be FDA\"/CE\"/DCGI approved |
| 20 | (S) FEMORAL SHEATH SYSTEMS SIZES 14F 7.5 cm with accessories for insertion.Should be FDA\"/CE\"/DCGI approved |
| 21 | (S) FEMORAL SHEATH SYSTEMS SIZES 14F 11 cm with accessories for insertion.Should be FDA\"/CE\"/DCGI approved |
| 22 | (S) FEMORAL SHEATH SYSTEMS SIZES 5F 23 cm with accessories for insertion.Should be FDA\"/CE\"/DCGI approved |
| 23 | (S) FEMORAL SHEATH SYSTEMS SIZES 6F 23 cm with accessories for insertion.Should be FDA\"/CE\"/DCGI approved |
| 24 | (S) FEMORAL SHEATH SYSTEMS SIZES 7F 23 cm with accessories for insertion.Should be FDA\"/CE\"/DCGI approved |
| 25 | (S) FEMORAL SHEATH SYSTEMS SIZES 8F 23 cm with accessories for insertion.Should be FDA\"/CE\"/DCGI approved |
| 26 | RADIAL ACCESS |
| 27 | (S) TRANSRADIAL SHEATH SYSTEMS with hydrophilic coating on the sheath, tapering hydrophilic dilator, hydrophilic straight polymer 018 wires and 20G plastic cannula for puncture 4F 7cm.Should be FDA\"/CE\"/DCGI approved |
| 28 | (S) TRANSRADIAL SHEATH SYSTEMS with hydrophilic coating on the sheath, tapering hydrophilic dilator, hydrophilic straight polymer 021 wires and 20G plastic cannula for puncture 4F 7cm.Should be FDA\"/CE\"/DCGI approved |
| 29 | (S) TRANSRADIAL SHEATH SYSTEMS with hydrophilic coating on the sheath, tapering hydrophilic dilator, hydrophilic straight polymer 025 wires and 20G plastic cannula for puncture 4F 7cm.Should be FDA\"/CE\"/DCGI approved |
| 30 | (S) TRANSRADIAL SHEATH SYSTEMS with hydrophilic coating on the sheath, tapering hydrophilicdilator hydrophilic straight polymer 018 wires and 20G plastic cannula for puncture 4F 11cm.Should be FDA\"/CE\"/DCGI approved |
| 31 | (S) TRANSRADIAL SHEATH SYSTEMS with hydrophilic coating on the sheath, tapering hydrophilicdilator hydrophilic straight polymer 021 wires and 20G plastic cannula for puncture 4F 11cm.Should be FDA\"/CE\"/DCGI approved |
| 32 | (S) TRANSRADIAL SHEATH SYSTEMS with hydrophilic coating on the sheath, tapering hydrophilicdilator hydrophilic straight polymer 025 wires and 20G plastic cannula for puncture 4F 11cm.Should be FDA\"/CE\"/DCGI approved |
| 33 | (S) TRANSRADIAL SHEATH SYSTEMS with hydrophilic coating on sheath, tapering dilator hydrophilic staright polymer 018 wires and 20G plastic cannula for puncture 5F 7cm.Should be FDA\"/CE\"/DCGI approved |
| 34 | (S) TRANSRADIAL SHEATH SYSTEMS with hydrophilic coating on sheath, tapering dilator hydrophilic staright polymer 021 wires and 20G plastic cannula for puncture 5F 7cm.Should be FDA\"/CE\"/DCGI approved |
| 35 | (S) TRANSRADIAL SHEATH SYSTEMS with hydrophilic coating on sheath, tapering dilator hydrophilic staright polymer 025 wires and 20G plastic cannula for puncture 5F 7cm.Should be FDA\"/CE\"/DCGI approved |
| 36 | (S) TRANSRADIAL SHEATH SYSTEMS with hydrophilic coating on sheath, tapering dilator hydrophilic staright polymer 018 wires and 20G plastic cannula for puncture 5F 11cm.Should be FDA\"/CE\"/DCGI approved |
| 37 | (S) TRANSRADIAL SHEATH SYSTEMS with hydrophilic coating on sheath, tapering dilator hydrophilic staright polymer 021 wires and 20G plastic cannula for puncture 5F 11cm.Should be FDA\"/CE\"/DCGI approved |
| 38 | (S) TRANSRADIAL SHEATH SYSTEMS with hydrophilic coating on sheath, tapering dilator hydrophilic staright polymer 025 wires and 20G plastic cannula for puncture 5F 11cm.Should be FDA\"/CE\"/DCGI approved |
| 39 | (S) TRANSRADIAL SHEATH SYSTEMS with hydrophilic coating on sheath, tapering dilator hydrophilic staright polymer 018 wires and 20G plastic cannula for puncture6F 7cm.Should be FDA\"/CE\"/DCGI approved |
| 40 | (S) TRANSRADIAL SHEATH SYSTEMS with hydrophilic coating on sheath, tapering dilator hydrophilic staright polymer 021 wires and 20G plastic cannula for puncture6F 7cm.Should be FDA\"/CE\"/DCGI approved |
| 41 | (S) TRANSRADIAL SHEATH SYSTEMS with hydrophilic coating on sheath, tapering dilator hydrophilic staright polymer 025 wires and 20G plastic cannula for puncture6F 7cm.Should be FDA\"/CE\"/DCGI approved |
| 42 | (S) TRANSRADIAL SHEATH SYSTEMS with hydrophilic coating on sheath, tapering dilator hydrophilic staright polymer 018 wires and 20G plastic cannula for puncture6F 11cm.Should be FDA\"/CE\"/DCGI approved |
| 43 | (S) TRANSRADIAL SHEATH SYSTEMS with hydrophilic coating on sheath, tapering dilator hydrophilic staright polymer 021 wires and 20G plastic cannula for puncture6F 11cm.Should be FDA\"/CE\"/DCGI approved |
| 44 | (S) TRANSRADIAL SHEATH SYSTEMS with hydrophilic coating on sheath, tapering dilator hydrophilic staright polymer 025 wires and 20G plastic cannula for puncture6F 11cm.Should be FDA\"/CE\"/DCGI approved |
| 45 | (S) TRANSRADIAL SHEATH SYSTEMS with hydrophilic coating on sheath, tapering dilator hydrophilic staright polymer 018 wires and 20G plastic cannula for puncture 7F 7cm.Should be FDA\"/CE\"/DCGI approved |
| 46 | (S) TRANSRADIAL SHEATH SYSTEMS with hydrophilic coating on sheath, tapering dilator hydrophilic staright polymer 021 wires and 20G plastic cannula for puncture 7F 7cm.Should be FDA\"/CE\"/DCGI approved |
| 47 | (S) TRANSRADIAL SHEATH SYSTEMS with hydrophilic coating on sheath, tapering dilator hydrophilic staright polymer 025 wires and 20G plastic cannula for puncture 7F 7cm.Should be FDA\"/CE\"/DCGI approved |
| 48 | (S) TRANSRADIAL SHEATH SYSTEMS with hydrophilic coating on sheath, tapering dilator hydrophilic staright polymer 018 wires and 20G plastic cannula for puncture 7F 11cm.Should be FDA\"/CE\"/DCGI approved |
| 49 | (S) TRANSRADIAL SHEATH SYSTEMS with hydrophilic coating on sheath, tapering dilator hydrophilic staright polymer 021 wires and 20G plastic cannula for puncture 7F 11cm.Should be FDA\"/CE\"/DCGI approved |
| 50 | (S) TRANSRADIAL SHEATH SYSTEMS with hydrophilic coating on sheath, tapering dilator hydrophilic staright polymer 025 wires and 20G plastic cannula for puncture 7F 11cm.Should be FDA\"/CE\"/DCGI approved |
| 51 | (S) TRANSRADIAL SLENDER SHEATH SYSTEMS 5F 10 cm capable of introducing 6F catheter with hydrophilic coating on sheath, tapering dilator hydrophilic staright polymer 021 wires and 20G plastic cannula for puncture .Should be FDA\"/CE\"/DCGI approved |
| 52 | (S) TRANSRADIAL SLENDER SHEATH SYSTEMS 5F 10 cm capable of introducing 6F catheter with hydrophilic coating on sheath, tapering dilator hydrophilic staright polymer 025 wires and 20G plastic cannula for puncture .Should be FDA\"/CE\"/DCGI approved |
| 53 | (S) TRANSRADIAL SLENDER SHEATH SYSTEMS 5F 16 cm capable of introducing 6F catheter with hydrophilic coating on sheath, tapering dilator hydrophilic staright polymer 021 wires and 20G plastic cannula for puncture .Should be FDA\"/CE\"/DCGI approved |
| 54 | (S) TRANSRADIAL SLENDERSHEATH SYSTEMS 6F 10 cm capable of introducing 7F catheter with hydrophilic coating on sheath, tapering dilator hydrophilic staright polymer 021 wires and 20G plastic cannula for puncture .Should be FDA\"/CE\"/DCGI approved |
| 55 | (S) TRANSRADIAL SLENDERSHEATH SYSTEMS 6F 10 cm capable of introducing 7F catheter with hydrophilic coating on sheath, tapering dilator hydrophilic staright polymer 025 wires and 20G plastic cannula for puncture .Should be FDA\"/CE\"/DCGI approved |
| 56 | (S) TRANSRADIAL SLENDERSHEATH SYSTEMS 6F16 cm capable of introducing 7F catheter with hydrophilic coating on sheath, tapering dilator hydrophilic staright polymer 021 wires and 20G plastic cannula for puncture .Should be FDA\"/CE\"/DCGI approved |
| 57 | (S) TRANSRADIAL SLENDERSHEATH SYSTEMS 7F 10 cm capable of introducing 8F catheter with hydrophilic coating on sheath, tapering dilator hydrophilic staright polymer 021 wires and 20G plastic cannula for puncture .Should be FDA\"/CE\"/DCGI approved |
| 58 | (S) TRANSRADIAL SLENDERSHEATH SYSTEMS 7F 10 cm capable of introducing 7F catheter with hydrophilic coating on sheath, tapering dilator hydrophilic staright polymer 025 wires and 20G plastic cannula for puncture .Should be FDA\"/CE\"/DCGI approved |
| 59 | (S) TRANSRADIAL SLENDERSHEATH SYSTEMS 7F16 cm capable of introducing 8F catheter with hydrophilic coating on sheath, tapering dilator hydrophilic staright polymer 021 wires and 20G plastic cannula for puncture .Should be FDA\"/CE\"/DCGI approved |
| 60 | ACCESS CLOSURE |
| 61 | (S) FEMORAL VASCULAR CLOSURE DEVICE Collagen Based Femoral 6F Should be FDA\"/CE\"/DCGI approved |
| 62 | (S) FEMORAL VASCULAR CLOSURE DEVICE Collagen Based Femoral8F Should be FDA\"/CE\"/DCGI approved |
| 63 | (S) FEMORAL VASCULAR CLOSURE DEVICE Prolene sutured capable of closing upto 21F devices.Should be FDA\" or CE\" andDCGI approved |
| 64 | (S) Collagen anchor based Femoral vascular closure device capable of closing large bore access ranging from 12 to 25 Fr.Should be FDA\"/CE\"/DCGI approved |
| 65 | (S) Radial Compression Device Balloon Inflation type transparent .Should be FDA\"/CE\"/DCGI approved |
| 66 | (S) Radial Compression Device Screw type .Should be FDA\"/CE\"/DCGI approved |
| 67 | (S) Polymer reinforced adhesive skin closure strips 6mm x 100mm |
| 68 | (S) Semipermeable waterproof plastic wound dressing with pad (Dressing size of 9 x 15cm and pad size 5 x 10cm) |
| 69 | DIAGNOSTIC CATHETERS |
| 70 | (S)COURNAND CATHETER 5F, 6F 110 cm woven dacron.Should be FDA\"/CE\"/DCGI approved |
| 71 | (S)GOODALE-LUBIN CATHETER 6F, 7F 100/125 cm woven dacron.Should be FDA/CE/DCGI approved |
| 72 | (S)JUDKINS LEFT CATHETER 4F 90/110 cm all Curves.Should be FDA\"/CE\"/DCGI approved |
| 73 | (S)JUDKINS LEFT CATHETER 5F,6F 110 cm all Curves.Should be FDA\"/CE\"/DCGI approved |
| 74 | (S)JUDKINS RIGHT CATHETER 4F, 90/110cm all Curves.Should be FDA\"/CE\"/DCGI approved |
| 75 | (S)JUDKINS RIGHT CATHETER 5F,6F 110cm all Curves.Should be FDA\"/CE\"/DCGI approved |
| 76 | (S)AMPLATZ LEFT CATHETER 4F 90/110cmall Curves.Should be FDA\"/CE\"/DCGI approved |
| 77 | (S)AMPLATZ LEFT CATHETER5F,6F 110cm all Curves.Should be FDA\"/CE\"/DCGI approved |
| 78 | (S)AMPLATZ RIGHT CATHETER 4F 90/110 cmall Curves.Should be FDA\"/CE\"/DCGI approved |
| 79 | (S)AMPLATZ RIGHT CATHETER 5F,6F 110cm all Curves.Should be FDA\"/CE\"/DCGI approved |
| 80 | (S)LEFT CORONARY BY PASS CATHETER 4F,5F,6F 110cm all Curves.Should be FDA\"/CE\"/DCGI approved |
| 81 | (S)RIGHT CORONARY BY PASS CATHETER 4F,5F,6F 110cm all Curves.Should be FDA\"/CE\"/DCGI approved |
| 82 | (S)INTERNAL MAMMARY ARTERY CATHETER 4F, 5F,6F 110cm all Curves.Should be FDA\"/CE\"/DCGI approved |
| 83 | (S)MULTIPURPOSE CATHETER 4F 90/110cm A1,A2,B1,B2.Should be FDA\"/CE\"/DCGI approved |
| 84 | (S)MULTIPURPOSE CATHETER 5F110cm A1,A2,B1,B2. Should be FDA\"/CE\"/DCGI approved |
| 85 | (S)MULTIPURPOSE CATHETER 6F 110cm A1,A2,B1,B2.Should be FDA\"/CE\"/DCGI approved |
| 86 | (S)RADIAL CAG TIG CATHETERS with Hydrophilic coating single side-hole 5F 100cmSMALL CURVES.Should be FDA\"/CE\"/DCGI approved |
| 87 | (S)RADIAL CAG TIG CATHETERS with Hydrophilic coating single side-hole5F 110cmSMALL CURVES.Should be FDA\"/CE\"/DCGI approved |
| 88 | (S)RADIAL CAG TIG CATHETERSwith Hydrophilic coating single side-hole 5F 100cmINTERMEDIATE CURVES.Should be FDA\"/CE\"/DCGI approved |
| 89 | (S)RADIAL CAG TIG CATHETERS with Hydrophilic coating single side-hole5F 110cmINTERMEDIATE CURVES.Should be FDA\"/CE\"/DCGI approved |
| 90 | (S)RADIAL CAG TIG CATHETERSwith Hydrophilic coating single side-hole 5F 100cmLARGE CURVES.Should be FDA\"/CE\"/DCGI approved |
| 91 | (S)RADIAL CAG TIG CATHETERS with Hydrophilic coating single side-hole5F 110cmLARGE CURVES.Should be FDA\"/CE\"/DCGI approved |
| 92 | (S)RADIAL CAG TIG CATHETERS with Hydrophilic coating single side-hole5F 100cmEXTRALARGE CURVES.Should be FDA\"/CE\"/DCGI approved |
| 93 | (S)RADIAL CAG TIG CATHETERSwith Hydrophilic coating single side-hole 5F 110cmEXTRALARGE CURVES.Should be FDA\"/CE\"/DCGI approved |
| 94 | (S)RADIAL CAG TIG CATHETERS with Hydrophilic coating two side-hole 5F 100cmSMALL CURVES.Should be FDA\"/CE\"/DCGI approved |
| 95 | (S)RADIAL CAG TIG CATHETERS with Hydrophilic coating two side-hole5F 110cmSMALL CURVES.Should be FDA\"/CE\"/DCGI approved |
| 96 | (S)RADIAL CAG TIG CATHETERSwith Hydrophilic coating two side-hole 5F 100cmINTERMEDIATE CURVES.Should be FDA\"/CE\"/DCGI approved |
| 97 | (S)RADIAL CAG TIG CATHETERS with Hydrophilic coating two side-hole5F 110cmINTERMEDIATE CURVES.Should be FDA\"/CE\"/DCGI approved |
| 98 | (S)RADIAL CAG TIG CATHETERSwith Hydrophilic coating two side-hole 5F 100cmLARGE CURVES.Should be FDA\"/CE\"/DCGI approved |
| 99 | (S)RADIAL CAG TIG CATHETERS with Hydrophilic coating two side-hole5F 110cmLARGE CURVES.Should be FDA\"/CE\"/DCGI approved |
| 100 | (S)RADIAL CAG TIG CATHETERS with Hydrophilic coating two side-hole5F 100cmEXTRALARGE CURVES.Should be FDA\"/CE\"/DCGI approved |
| 101 | (S)RADIAL CAG TIG CATHETERSwith Hydrophilic coating two side-hole 5F 110cmEXTRALARGE CURVES.Should be FDA\"/CE\"/DCGI approved |
| 102 | ( S) PIG TAIL CATHETERS4F 90cm.Should be FDA\"/CE\"/DCGI approved |
| 103 | ( S) PIG TAIL CATHETERS4F 110cm.Should be FDA\"/CE\"/DCGI approved |
| 104 | ( S) PIG TAIL CATHETERS4F 150cm.Should be FDA\"/CE\"/DCGI approved |
| 105 | ( S) PIG TAIL CATHETERS 5F 90cm.Should be FDA\"/CE\"/DCGI approved |
| 106 | ( S) PIG TAIL CATHETERS5F 110cm.Should be FDA\"/CE\"/DCGI approved |
| 107 | ( S) PIG TAIL CATHETERS5F 150cm.Should be FDA\"/CE\"/DCGI approved |
| 108 | ( S) PIG TAIL CATHETERS6F 90cm.Should be FDA\"/CE\"/DCGI approved |
| 109 | ( S) PIG TAIL CATHETERS6F 110cm.Should be FDA\"/CE\"/DCGI approved |
| 110 | ( S) PIG TAIL CATHETERS6F 150cm.Should be FDA\"/CE\"/DCGI approved |
| 111 | ( S) ANGLED PIG TAIL CATHETERS4F 90cm.Should be FDA\"/CE\"/DCGI approved |
| 112 | ( S) ANGLED PIG TAIL CATHETERS4F 110cm.Should be FDA\"/CE\"/DCGI approved |
| 113 | ( S) ANGLED PIG TAIL CATHETERS4F 150cm.Should be FDA\"/CE\"/DCGI approved |
| 114 | ( S) ANGLED PIG TAIL CATHETERS5F 90cm.Should be FDA\"/CE\"/DCGI approved |
| 115 | ( S) ANGLED PIG TAIL CATHETERS5F 110cm.Should be FDA\"/CE\"/DCGI approved |
| 116 | ( S) ANGLED PIG TAIL CATHETERS5F 150cm.Should be FDA\"/CE\"/DCGI approved |
| 117 | ( S) ANGLED PIG TAIL CATHETERS6F 90cm.Should be FDA\"/CE\"/DCGI approved |
| 118 | ( S) ANGLED PIG TAIL CATHETERS6F 110cm.Should be FDA\"/CE\"/DCGI approved |
| 119 | ( S) ANGLED PIG TAIL CATHETERS6F 150cm.Should be FDA\"/CE\"/DCGI approved |
| 120 | ( S)MARKERPIGTAIL CATHETER 4F 90cm. Should be FDA\"/CE\"/DCGI approved |
| 121 | ( S) MARKERPIGTAIL CATHETER 4F 110cm .Should be FDA\"/CE\"/DCGI approved |
| 122 | ( S) MARKERPIGTAIL CATHETER 4F 150cm .Should be FDA\"/CE\"/DCGI approved |
| 123 | ( S) MARKERPIGTAIL CATHETER 5F 90cm .Should be FDA\"/CE\"/DCGI approved |
| 124 | ( S) MARKERPIGTAIL CATHETER 5F 110cm .Should be FDA\"/CE\"/DCGI approved |
| 125 | ( S) MARKERPIGTAIL CATHETER 5F 150cm .Should be FDA\"/CE\"/DCGI approved |
| 126 | ( S) MARKERPIGTAIL CATHETER 6F 90cm .Should be FDA\"/CE\"/DCGI approved |
| 127 | ( S) MARKERPIGTAIL CATHETER 6F 110cm .Should be FDA\"/CE\"/DCGI approved |
| 128 | ( S) MARKERPIGTAIL CATHETER 6F 150cm .Should be FDA\"/CE\"/DCGI approved |
| 129 | NIH Angiography catheter 4FShould be FDA\"/CE\"/DCGI approved |
| 130 | NIH Angiography catheter 5F/6F Should be FDA\"/CE\"/DCGI approved |
| 131 | BERMAN Angiography catheter 4F 60/90/110 cm Should be FDA\"/CE\"/DCGI approved |
| 132 | BERMAN Angiography catheter 5F and 6F60/90/110 cm Should be FDA\"/CE\"/DCGI approved |
| 133 | REVERSE BERMAN Angiography catheter 4F 60/90/110 cm Should be FDA\"/CE\"/DCGI approved |
| 134 | REVERSE BERMAN Angiography catheter 4F 60/90/110 cm Should be FDA\"/CE\"/DCGI approved |
| 135 | MULTITRACK Angiography Cathetercapable of doing angiography with guidewire insitu4F 80/100cmShould be FDA\"/CE\"/DCGI approved |
| 136 | MULTITRACK Angiography Catheter capable of doing angiography with guidewire insitu 5F 80/100cm Should be FDA\"/CE\"/DCGI approved |
| 137 | MULTITRACK Angiography Catheter capable of doing angiography with guidewire insitu 6F 80/100cm Should be FDA\"/CE\"/DCGI approved |
| 138 | ACCESSORIES |
| 139 | (S) INITIAL PUNCTURE NEEDLES18G Should be FDA\"/CE\"/DCGI approved |
| 140 | (S) MICROPUNCTURE NEONATAL INTRODUCER SETS AND SHEATH SYSTEMS 4F Should be FDA\"/CE\"/DCGI approved |
| 141 | (S) MICROPUNCTURE NEONATAL INTRODUCER SETS AND SHEATH SYSTEMS 5F.Should be FDA\"/CE\"/DCGI approved |
| 142 | (S) Micropuncture introducer set suitable for ultrasound guided vascular access.Should include one 21G 7cm micropuncture needle, one 0.18\" guide wire and one 5F introducer sheath as one set |
| 143 | (S) 3/3 ROTATING MANIFOLD FOR CAG.Should be FDA\"/CE\"/DCGI approved |
| 144 | (S) 3/3 ROTATING MANIFOLD FOR PTCA.Should be FDA\"/CE\"/DCGI approved |
| 145 | (S) TOUHEY BORST Y CONNECTOR- PUSH PULL TYPE and INTRODUCER NEEDLE for PTCA.Should be FDA\"/CE\"/DCGI approved |
| 146 | (S) TOUHEY BORST Y CONNECTOR- SCREW TYPE and INTRODUCER NEEDLE for PTCA.Should be FDA\"/CE\"/DCGI approved |
| 147 | (S) Y CONNECTOR 10F Diameter having a larger inner lumen for peripheral interventions.Should be FDA\"/CE\"/DCGI approved |
| 148 | (S) Torquer device for 014 guide wire |
| 149 | (S) Torquer device for 018 guide wire |
| 150 | (S) Torquer device for 021 guide wire |
| 151 | (S) Torquer device for 025 guide wire |
| 152 | (S) Torquer device for 035 guide wire |
| 153 | (S) Torquer device for 038 guide wire |
| 154 | ( S)PRESSURE MANOMETER LINES MALE/FEMALE 150 CM.Should be FDA\"/CE\"/DCGI approved |
| 155 | (S)PRESSURE MANOMETER LINES MALE/MALE 150 CM.Should be FDA\"/CE\"/DCGI approved |
| 156 | (S)THREE WAY STOPCOCKS.Should be FDA\"/CE\"/DCGI approved |
| 157 | (S)HIGH PRESSURE CONTRAST INJECTION TUBE.Should be FDA\"/CE\"/DCGI approved |
| 158 | (S)HIGH FLOW ANGIO FLUSH CATHS.Should be FDA\"/CE\"/DCGI approved |
| 159 | (S) 3 RING CONTROL SYRINGES 20cc.Should be FDA\"/CE\"/DCGI approved |
| 160 | (S) 3 RING CONTROL SYRINGES TRANSPARENT WITH MARKERS 20cc.Should be DCGI approved |
| 161 | ( S) FEMORALANGIOGRAPHY KITS Comprising the following Items a.Femoral Sheath Insertion System 6F 11cm b. Femoral Angiography 6F JL4 and JR3.5catheters ( one each) c. 0.035 J Hydrophilic teflon wire, d.Disposable Sterile Drape for Radial/Femoral angiography e.Disposable Sterile Gowns -2, f.Disposable Gloves-2, g.Finger control syringe 20cc h.3/3 Rotating manifold i.pressure line j.100 mL Non-Ionic contrast media with320 mg iodine/mL.Should be FDA\"/CE\"/DCGI approved |
| 162 | (S) RADIAL ANGIO SET WITH PUNCTURE NEEDLE, SHEATH 6F 7cm, STRAIGHT GUIDEWIRE 025/021AND TIG coronary diagnosticcatheter 5F, AND HYDROPHILIC POLYMER J tipped 035 145 cm WIRES.Should be FDA\"/CE\"/DCGI approved |
| 163 | ( S) RADIAL ANGIOGRAPHY KITS Comprising the following Items a.Radial Sheath Insertion System 6F 7cmb. Radial Angiography 5F TIG catheter c. 0.035 J Hydrophilic polymer wire, d.Disposable Sterile Drape for Radial/Femoral angiography e.Disposable Sterile Gowns -2, f.Disposable Gloves-2, g.Finger control syringe 20cc h.3/3 Rotating manifold i.pressure line j.100 mL Non-Ionic contrast media 320mg iodine/mL.Should be FDA\"/CE\"/DCGI approved |
| 164 | (S) FEMORAL ANGIOPLASTY KIT (1stent) 1. Disposable Cath-Lab Gowns Light Blue Colour full size and elastic wrist bands with water\"/ blood impenetrable front and hand shielding - 3 Nos2.DISPOSABLE STERILE DRAPES FOR CORONARY ANGIOGRAPHY\"\" / ANGIOPLASTY COMPATIBLE WITH Bilateral FEMORAL and RADIAL APPROACHES - 1No3.DISPOSABLEGAUZE PIECES in ( ETO Sterilizable)PACKS OF 10 for use with Cath Lab procedures - 10Nos4.TEFLON COATED GUIDE WIRES 145 CMS 0.035\"ST & J - 1No5.Arterial Pressure monitoring Transducers (Disposable) - 1No6.INITIAL PUNCTURE NEEDLES18G - 1No7.FEMORAL PCI SHEATH SYSTEMS SIZE 5F to 9Fwith accessories for insertion - 2Nos8. PTCA WIRE - 1 No9.3 RING CONTROL SYRINGES FOR CAG\"/PTCA 20cc - 1No10. 3\"/3 ROTATING MANIFOLD FOR CAG\"/PTCA-1No 11. TOUHEY BORST Y CONNECTOR- PUSH PULL TYPE and INTRODUCER NEEDLE for PTCA - 1No12.PTCA GUIDING CATHETER - 1No13.3 Ring Finger Control syringe 12 cc - 1No14.INFUSION ACCELERATOR ( PRESSURE BAG) -1No15.Rapid Exchange BalloonSystems with Semi-Compliant\"/Compliant Design with Excellent Trackability and High Inflation Pressures - 1No16.Non-Compliant Balloons for PTCA - 1No17.DRUG ELUTING STENTS FDA/ DCGI /CE APPROVED-1 No.Should be FDA\"/CE\"/DCGI approved |
| 165 | (S)FEMORAL ANGIOPLASTY KIT(2 Stent)1. Disposable Cath-Lab Gowns Light Blue Colour full size and elastic wrist bands with water\"/ blood impenetrable front and hand shielding - 3 Nos2.DISPOSABLE STERILE DRAPES FOR CORONARY ANGIOGRAPHY\"\" / ANGIOPLASTY COMPATIBLE WITH Bilateral FEMORAL and RADIAL APPROACHES - 1No3.DISPOSABLEGAUZE PIECES in ( ETO Sterilizable)PACKS OF 10 for use with Cath Lab procedures - 10Nos4.TEFLON COATED GUIDE WIRES 145 CMS 0.035\"ST & J - 1No5.Arterial Pressure monitoring Transducers (Disposable) - 1No6.INITIAL PUNCTURE NEEDLES18G - 1No7.FEMORAL PCI SHEATH SYSTEMS SIZE 5F to 9Fwith accessories for insertion - 2Nos8. PTCA WIRE- 1 No9.3 RING CONTROL SYRINGES FOR CAG\"/PTCA 20cc - 1No10. 3\"/3 ROTATING MANIFOLD FOR CAG\"/PTCA-1No 11. TOUHEY BORST Y CONNECTOR- PUSH PULL TYPE and INTRODUCER NEEDLE for PTCA - 1No12.PTCA GUIDING CATHETER - 1No13.3 Ring Finger Control syringe 12 cc - 1No14.INFUSION ACCELERATOR ( PRESSURE BAG) -1No15.Rapid Exchange BalloonSystems with Semi-Compliant\"/Compliant Design with Excellent Trackability and High Inflation Pressures - 1No16.Non-Compliant Balloons for PTCA - 1No17.DRUG ELUTING STENTS FDA/ DCGI /CE -2 Nos.Should be FDA\"/CE\"/DCGI approved |
| 166 | (S)RADIAL ANGIOPLASTY KIT (1 Stent) 1. Disposable Cath-Lab Gowns Light Blue Colour full size and elastic wrist bands with water\"/ blood impenetrable front and hand shielding - 3 Nos2.DISPOSABLE STERILE DRAPES FOR CORONARY ANGIOGRAPHY\"\" / ANGIOPLASTY COMPATIBLE WITH Bilateral FEMORAL and RADIAL APPROACHES - 1No3.DISPOSABLEGAUZE PIECES in ( ETO Sterilizable)PACKS OF 10 for use with Cath Lab procedures - 10Nos4.TEFLON COATED GUIDE WIRES 145 CMS 0.035\"ST & J - 1No5.Arterial Pressure monitoring Transducers (Disposable) - 1No6.INITIAL PUNCTURE NEEDLES18G - 1No7.TRANSRADIAL SHEATH SYSTEMS SIZE 6F with accessories for insertion - 1Nos8. PTCA WIRE - 1 No9.3 RING CONTROL SYRINGES FOR CAG\"/PTCA 20cc - 1No10. 3\"/3 ROTATING MANIFOLD FOR CAG\"/PTCA-1No 11. TOUHEY BORST Y CONNECTOR- PUSH PULL TYPE and INTRODUCER NEEDLE for PTCA - 1No12.PTCA GUIDING CATHETER - 1No13.3 Ring Finger Control syringe 12 cc - 1No14.INFUSION ACCELERATOR ( PRESSURE BAG) -1No15.Rapid Exchange BalloonSystems with Semi-Compliant\"/Compliant Design with Excellent Trackability and High Inflation Pressures - 1No16.Non-Compliant Balloons for PTCA - 1No17.DRUG ELUTING STENTS FDA / DCGI/CE APPROVED -1 No.Should be FDA\"/CE\"/DCGI approved |
| 167 | (S)RADIAL ANGIOPLASTY KIT(2 Stent)1. Disposable Cath-Lab Gowns Light Blue Colour full size and elastic wrist bands with water\"/ blood impenetrable front and hand shielding - 3 Nos2.DISPOSABLE STERILE DRAPES FOR CORONARY ANGIOGRAPHY\"\" / ANGIOPLASTY COMPATIBLE WITH Bilateral FEMORAL and RADIAL APPROACHES - 1No3.DISPOSABLEGAUZE PIECES in ( ETO Sterilizable)PACKS OF 10 for use with Cath Lab procedures - 10Nos4.TEFLON COATED GUIDE WIRES 145 CMS 0.035\"ST & J - 1No5.Arterial Pressure monitoring Transducers (Disposable) - 1No6.INITIAL PUNCTURE NEEDLES18G - 1No7.TRANSRADIAL SHEATH SYSTEMS SIZE 6F with accessories for insertion - 1Nos8. PTCA WIRE - 1 No9.3 RING CONTROL SYRINGES FOR CAG\"/PTCA 20cc - 1No10. 3\"/3 ROTATING MANIFOLD FOR CAG\"/PTCA-1No 11. TOUHEY BORST Y CONNECTOR- PUSH PULL TYPE and INTRODUCER NEEDLE for PTCA - 1No12.PTCA GUIDING CATHETER - 1No13.3 Ring Finger Control syringe 12 cc - 1No14.INFUSION ACCELERATOR ( PRESSURE BAG) -1No15.Rapid Exchange BalloonSystems with Semi-Compliant\"/Compliant Design with Excellent Trackability and High Inflation Pressures - 1No16.Non-Compliant Balloons for PTCA - 1No17.DRUG ELUTING STENT FDA/ DCGI/CE APPROVED -2 No.Should be FDA\"/CE\"/DCGI approved |
| 168 | (S) 20CC INFLATION DEVICEAS ONE SET capable of inflation pressures upto 30 bar.Should be FDA\"/CE\"/DCGI approved |
| 169 | (S) 20CC INFLATION DEVICEAS ONE SET capable of inflation pressures upto 25 bar.Should be FDA\"/CE\"/DCGI approved |
| 170 | ( S)INFLATION DEVICE TO INFLATE HIGH PRESSURE UPTO 50 ATM.Should be FDA\"/CE\"/DCGI approved |
| 171 | (S) PTCA MANIFOLD WITH FLUSH DEVICE.Should be FDA\"/CE\"/DCGI approved |
| 172 | (S) INFUSION ACCELERATOR ( PRESSURE BAG).Should be FDA\"/CE\"/DCGI approved |
| 173 | ( S) 3 RING CONTROL SYRINGES FOR CAG/PTCA 12cc.Should be FDA\"/CE\"/DCGI approved |
| 174 | ( S) 3 RING CONTROL SYRINGES FOR CAG/PTCA 20cc.Should be FDA\"/CE\"/DCGI approved |
| 175 | GUIDEWIRES |
| 176 | (S)TEFLON COATED GUIDE WIRE 145 CM 0.021\" ST. Should be FDA\"/CE\"/DCGI approved |
| 177 | (S)TEFLON COATED GUIDE WIRE 145 CM 0.021\" J. Should be FDA\"/CE\"/DCGI approved |
| 178 | (S)TEFLON COATED GUIDE WIRE 145 CM 0.025\" ST. Should be FDA\"/CE\"/DCGI approved |
| 179 | (S)TEFLON COATED GUIDE WIRE 145 CM 0.025\" J. Should be FDA\"/CE\"/DCGI approved |
| 180 | (S)TEFLON COATED GUIDE WIRES 145 CM0.032\"ST. Should be FDA\"/CE\"/DCGI approved |
| 181 | (S)TEFLON COATED GUIDE WIRES 145 CM0.032\"J. Should be FDA\"/CE\"/DCGI approved |
| 182 | (S)TEFLON COATED GUIDE WIRES 145 CMS 0.035\" ST. Should be FDA\"/CE\"/DCGI approved |
| 183 | (S)TEFLON COATED GUIDE WIRES 145 CMS 0.035\" J. Should be FDA\"/CE\"/DCGI approved |
| 184 | (S)TEFLON COATED GUIDE WIRES 145 CMS 0.038\" ST. Should be FDA\"/CE\"/DCGI approved |
| 185 | (S)TEFLON COATED GUIDE WIRES 145 CMS 0.038\" J. Should be FDA\"/CE\"/DCGI approved |
| 186 | ( S) TEFLON COATED EXCHANGE (260cm and above)0.018\"\" ST peripheral guide wire .Should be FDA\"/CE\"/DCGI approved |
| 187 | ( S) TEFLON COATED EXCHANGE (260cm and above)0.018\"\" J peripheral guide wire .Should be FDA\"/CE\"/DCGI approved |
| 188 | ( S) TEFLON COATED EXCHANGE (260cm and above)0.021\"\" ST peripheral guide wire .Should be FDA\"/CE\"/DCGI approved |
| 189 | ( S) TEFLON COATED EXCHANGE (260cm and above)0.021\"\" J peripheral guide wire .Should be FDA\"/CE\"/DCGI approved |
| 190 | (S)TEFLON COATED EXCHANGE GUIDE WIRE (260cm and above)0.032\"ST.Should be FDA\"/CE\"/DCGI approved |
| 191 | (S)TEFLON COATED EXCHANGE GUIDE WIRE (260cm and above)0.032\" J.Should be FDA\"/CE\"/DCGI approved |
| 192 | (S)TEFLON COATED EXCHANGE GUIDE WIRE (260cm and above)0.035\"ST.Should be FDA\"/CE\"/DCGI approved |
| 193 | (S)TEFLON COATED EXCHANGE GUIDE WIRE (260cm and above)0.035\" J.Should be FDA\"/CE\"/DCGI approved |
| 194 | (S)TEFLON COATED EXCHANGEGUIDE WIRE (260cm and above)0.038\"ST.Should be FDA\"/CE\"/DCGI approved |
| 195 | (S)TEFLON COATED EXCHANGE GUIDE WIRE (260cm and above)0.038\"J.Should be FDA\"/CE\"/DCGI approved |
| 196 | ( S)Lunderquist type high support exchange length 0.035\"\" (260cm and above) short and long floppy tip guide wire. Should be FDA\"/CE\"/DCGI approved |
| 197 | ( S)Safari type high support exchange length 0.035\"\" (260cm and above)curvedtip guide wire. Should be FDA\"/CE\"/DCGI approved |
| 198 | ( S)Confida type intermediatesupport exchange length 0.035\"\" (260cm and above) J tip guide wire. Should be FDA\"/CE\"/DCGI approved |
| 199 | ( S)Roadrunner type extrasupportexchange length 0.035\"\" (260cm and above) Straight tip guide wire with hydrophilic coating . Should be FDA\"/CE\"/DCGI approved |
| 200 | ( S)Roadrunner type extrasupportexchange length 0.035\"\" (260cm and above) J tip guide wire with hydrophilic coating . Should be FDA\"/CE\"/DCGI approved |
| 201 | ( S)AMPLATZ SUPERSTIFF EXCHANGE GUIDE WIRES 0.035\". 260 cm and above- Short floppy tip.Should be FDA\"/CE\"/DCGI approved |
| 202 | ( S)AMPLATZ SUPERSTIFF EXCHANGE GUIDE WIRES .038\"\". 260 cm and above- Short floppy tip.Should be FDA\"/CE\"/DCGI approved |
| 203 | ( S)AMPLATZ ULTRA STIFF EXCHANGE GUIDE WIRES 0.035\" J. 260 cm and above- LONG floppy tip.Should be FDA\"/CE\"/DCGI approved |
| 204 | ( S)AMPLATZ ULTRA STIFF EXCHANGE GUIDE WIRES0.038\"\"J. 260 cm and above- LONG floppy tip.Should be FDA\"/CE\"/DCGI approved |
| 205 | ( S) AMPLATZ NOODLE TYPE EXCHANGE Guidewire PTFE coated Stainless Steel wire 0.035\" J. 260 cm and above |
| 206 | ( S)TERUMO HYDROPHILIC GUIDE WIRES 145 CM 018 ST.Should be FDA\"/CE\"/DCGI approved |
| 207 | ( S)TERUMO HYDROPHILIC GUIDE WIRES 145 CM 018 J.Should be FDA\"/CE\"/DCGI approved |
| 208 | ( S)TERUMO HYDROPHILIC GUIDE WIRES 145 CM 021 ST.Should be FDA\"/CE\"/DCGI approved |
| 209 | ( S)TERUMO HYDROPHILIC GUIDE WIRES 145 CM 021 J.Should be FDA\"/CE\"/DCGI approved |
| 210 | ( S)TERUMO HYDROPHILIC GUIDE WIRES 145 CM 025 ST.Should be FDA\"/CE\"/DCGI approved |
| 211 | ( S)TERUMO HYDROPHILIC GUIDE WIRES 145 CM 025 J.Should be FDA\"/CE\"/DCGI approved |
| 212 | ( S)TERUMO HYDROPHILIC GUIDE WIRES 145 CM 032 ST.Should be FDA\"/CE\"/DCGI approved |
| 213 | ( S)TERUMO HYDROPHILIC GUIDE WIRES 145 CM 032 J.Should be FDA\"/CE\"/DCGI approved |
| 214 | ( S)TERUMO HYDROPHILIC GUIDE WIRES 145 CM 035 ST.Should be FDA\"/CE\"/DCGI approved |
| 215 | ( S)TERUMO HYDROPHILIC GUIDE WIRES 145 CM 035 J.Should be FDA\"/CE\"/DCGI approved |
| 216 | ( S)TERUMO EXCHANGE LENGTH GUIDE WIRES 260CM 018 ST.Should be FDA\"/CE\"/DCGI approved |
| 217 | ( S)TERUMO EXCHANGE LENGTH GUIDE WIRES 260CM 018 J.Should be FDA\"/CE\"/DCGI approved |
| 218 | ( S)TERUMO EXCHANGE LENGTH GUIDE WIRES 260CM 021 ST.Should be FDA\"/CE\"/DCGI approved |
| 219 | ( S)TERUMO EXCHANGE LENGTH GUIDE WIRES 260CM 021 J.Should be FDA\"/CE\"/DCGI approved |
| 220 | ( S)TERUMO EXCHANGE LENGTH GUIDE WIRES 260CM 025 ST.Should be FDA\"/CE\"/DCGI approved |
| 221 | ( S)TERUMO EXCHANGE LENGTH GUIDE WIRES 260CM 025 J.Should be FDA\"/CE\"/DCGI approved |
| 222 | ( S)TERUMO EXCHANGE LENGTH GUIDE WIRES 260CM 032 ST.Should be FDA\"/CE\"/DCGI approved |
| 223 | ( S)TERUMO EXCHANGE LENGTH GUIDE WIRES 260CM 032 J.Should be FDA\"/CE\"/DCGI approved |
| 224 | ( S)TERUMO EXCHANGE LENGTH GUIDE WIRES 260CM 035 ST.Should be FDA\"/CE\"/DCGI approved |
| 225 | ( S)TERUMO EXCHANGE LENGTH GUIDE WIRES 260CM 035 J.Should be FDA\"/CE\"/DCGI approved |
| 226 | GUIDING CATHETERS |
| 227 | (S)(EX)PTCA GUIDING CATHETER 4F JR 3.0 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 228 | (S) (EX)PTCA GUIDING CATHETER 5F JR 3.0 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 229 | (S) (EX)PTCA GUIDING CATHETER 6F JR 3.0 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 230 | (S)(EX)PTCA GUIDING CATHETER 7F JR 3.0 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 231 | (S)(EX)PTCA GUIDING CATHETER 8F JR 3.0 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 232 | (S)(EX)PTCA GUIDING CATHETER 4F JL 2.0 CURVE. Should be FDA\"/CE\"/DCGI approved |
| 233 | (S)(EX)PTCA GUIDING CATHETER 5F JL 2.0 CURVE. Should be FDA\"/CE\"/DCGI approved |
| 234 | (S)(EX)PTCA GUIDING CATHETER 6F JL 2.0 CURVE. Should be FDA\"/CE\"/DCGI approved |
| 235 | (S)(EX)PTCA GUIDING CATHETER 7F JL 2.0 CURVE. Should be FDA\"/CE\"/DCGI approved |
| 236 | (S)(EX)PTCA GUIDING CATHETER 8F JL 2.0 CURVE. Should be FDA\"/CE\"/DCGI approved |
| 237 | (S)(EX)PTCA GUIDING CATHETER 4F JL 3.0 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 238 | (S)(EX)PTCA GUIDING CATHETER 5F JL 3.0 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 239 | (S)(EX)PTCA GUIDING CATHETER 6F JL 3.0 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 240 | (S)(EX)PTCA GUIDING CATHETER 7F JL 3.0 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 241 | (S)(EX)PTCA GUIDING CATHETER 8F JL 3.0 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 242 | (S)(EX)PTCA GUIDING CATHETER 4F JR 3.5 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 243 | (S)(EX)PTCA GUIDING CATHETER 5F JR 3.5 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 244 | (S)(EX)PTCA GUIDING CATHETER 6F JR 3.5 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 245 | (S)(EX)PTCA GUIDING CATHETER 7F JR 3.5 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 246 | (S)(EX)PTCA GUIDING CATHETER 8F JR 3.5 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 247 | (S)(EX)PTCA GUIDING CATHETER 4F JL 3.5 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 248 | (S)(EX)PTCA GUIDING CATHETER 5F JL 3.5 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 249 | (S)(EX)PTCA GUIDING CATHETER 6F JL 3.5 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 250 | (S)(EX)PTCA GUIDING CATHETER 7F JL 3.5 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 251 | (S)(EX)PTCA GUIDING CATHETER 8F JL 3.5 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 252 | (S)(EX)PTCA GUIDING CATHETER 4F JR 4.0 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 253 | (S)(EX)PTCA GUIDING CATHETER 5F JR 4.0 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 254 | (S)(EX)PTCA GUIDING CATHETER 6F JR 4.0 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 255 | (S)(EX)PTCA GUIDING CATHETER 7F JR 4.0 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 256 | (S)(EX)PTCA GUIDING CATHETER 8F JR 4.0 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 257 | (S)(EX)PTCA GUIDING CATHETER 4F JL 4.0 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 258 | (S)(EX)PTCA GUIDING CATHETER 5F JL 4.0 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 259 | (S)(EX)PTCA GUIDING CATHETER 6F JL 4.0 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 260 | (S)(EX)PTCA GUIDING CATHETER 7F JL 4.0 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 261 | (S)(EX)PTCA GUIDING CATHETER 8F JL 4.0 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 262 | (S)(EX)PTCA GUIDING CATHETER 4F JR 4.5 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 263 | (S)(EX)PTCA GUIDING CATHETER 5F JR 4.5 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 264 | (S)(EX)PTCA GUIDING CATHETER 6F JR 4.5 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 265 | (S)(EX)PTCA GUIDING CATHETER 7F JR 4.5 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 266 | (S)(EX)PTCA GUIDING CATHETER 8F JR 4.5 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 267 | (S)(EX)PTCA GUIDING CATHETER 4F JL 4.5 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 268 | (S)(EX)PTCA GUIDING CATHETER 5F JL 4.5 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 269 | (S)(EX)PTCA GUIDING CATHETER 6F JL 4.5 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 270 | (S)(EX)PTCA GUIDING CATHETER 7F JL 4.5 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 271 | (S)(EX)PTCA GUIDING CATHETER 8F JL 4.5 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 272 | (S)(EX)PTCA GUIDING CATHETER 4F JR 5.0 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 273 | (S)(EX)PTCA GUIDING CATHETER 5F JR 5.0 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 274 | (S)(EX)PTCA GUIDING CATHETER 6F JR 5.0 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 275 | (S)(EX)PTCA GUIDING CATHETER 7F JR 5.0 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 276 | (S)(EX)PTCA GUIDING CATHETER 8F JR 5.0 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 277 | (S)(EX)PTCA GUIDING CATHETER 4F JL 5.0 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 278 | (S)(EX)PTCA GUIDING CATHETER 5F JL 5.0 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 279 | (S)(EX)PTCA GUIDING CATHETER 6F JL 5.0 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 280 | (S)(EX)PTCA GUIDING CATHETER 7F JL 5.0 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 281 | (S)(EX)PTCA GUIDING CATHETER 8F JL 5.0 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 282 | (S)(EX)PTCA GUIDING CATHETER 4F EBU 3.0 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 283 | (S)(EX)PTCA GUIDING CATHETER 5F EBU 3.0 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 284 | (S)(EX)PTCA GUIDING CATHETER 5F EBU 2.0 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 285 | (S)(EX)PTCA GUIDING CATHETER 6F EBU 2.0 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 286 | (S)(EX)PTCA GUIDING CATHETER 6F EBU 3.0 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 287 | (S)(EX)PTCA GUIDING CATHETER 7F EBU 3.0 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 288 | (S)(EX)PTCA GUIDING CATHETER 8F EBU 3.0 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 289 | (S)(EX)PTCA GUIDING CATHETER 4F EBU 3.5 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 290 | (S)(EX)PTCA GUIDING CATHETER 5F EBU 3.5 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 291 | (S)(EX)PTCA GUIDING CATHETER 6F EBU 3.5 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 292 | (S)(EX)PTCA GUIDING CATHETER 7F EBU 3.5 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 293 | (S)(EX)PTCA GUIDING CATHETER 8F EBU 3.5 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 294 | (S)(EX)PTCA GUIDING CATHETER 4F EBU 3.75 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 295 | (S)(EX)PTCA GUIDING CATHETER 5F EBU 3.75 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 296 | (S)(EX)PTCA GUIDING CATHETER 6F EBU 3.75 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 297 | (S)(EX)PTCA GUIDING CATHETER 7F EBU 3.75 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 298 | (S)(EX)PTCA GUIDING CATHETER 8F EBU 3.75 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 299 | (S)(EX)PTCA GUIDING CATHETER 4F EBU 4.0 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 300 | (S)(EX)PTCA GUIDING CATHETER 5F EBU 4.0 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 301 | (S)(EX)PTCA GUIDING CATHETER 6F EBU 4.0 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 302 | (S)(EX)PTCA GUIDING CATHETER 7F EBU 4.0 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 303 | (S)(EX)PTCA GUIDING CATHETER 8F EBU 4.0 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 304 | (S)(EX)PTCA GUIDING CATHETER 4F XB 3.0 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 305 | (S)(EX)PTCA GUIDING CATHETER 5F XB 2.5 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 306 | (S)(EX)PTCA GUIDING CATHETER 5F XB 3.0 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 307 | (S)(EX)PTCA GUIDING CATHETER 6F XB 2.5 CURVE. Should be FDA\"/CE\"/DCGI approved |
| 308 | (S)(EX)PTCA GUIDING CATHETER 6F XB 3.0 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 309 | (S)(EX)PTCA GUIDING CATHETER 7F XB 3.0 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 310 | (S)(EX)PTCA GUIDING CATHETER 8F XB 3.0 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 311 | (S)(EX)PTCA GUIDING CATHETER 4F XB 3.5 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 312 | (S)(EX)PTCA GUIDING CATHETER 5F XB 3.5 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 313 | (S)(EX)PTCA GUIDING CATHETER 6F XB 3.5 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 314 | (S)(EX)PTCA GUIDING CATHETER 7F XB 3.5 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 315 | (S)(EX)PTCA GUIDING CATHETER 8F XB 3.5 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 316 | (S)(EX)PTCA GUIDING CATHETER 4F XB 4.0 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 317 | (EX)PTCA GUIDING CATHETER 5F XB 4.0 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 318 | (EX)PTCA GUIDING CATHETER 6F XB 4.0 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 319 | (EX)PTCA GUIDING CATHETER 7F XB 4.0 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 320 | (EX)PTCA GUIDING CATHETER 8F XB 4.0 CURVE.Should be FDA\"/CE\"/DCGI approved |
| 321 | (EX)PTCA GUIDING CATHETER 4F MP ALL CURVES.Should be FDA\"/CE\"/DCGI approved |
| 322 | (EX)PTCA GUIDING CATHETER 5F MP ALL CURVES.Should be FDA\"/CE\"/DCGI approved |
| 323 | (EX)PTCA GUIDING CATHETER 6F MP ALL CURVES.Should be FDA\"/CE\"/DCGI approved |
| 324 | (EX)PTCA GUIDING CATHETER 7F MP ALL CURVES.Should be FDA\"/CE\"/DCGI approved |
| 325 | (EX)PTCA GUIDING CATHETER 8F MP ALL CURVES.Should be FDA\"/CE\"/DCGI approved |
| 326 | (EX)PTCA GUIDING CATHETER 4F CLS 3.0.Should be FDA\"/CE\"/DCGI approved |
| 327 | (EX)PTCA GUIDING CATHETER 5F CLS 3.0Should be FDA\"/CE\"/DCGI approved |
| 328 | (EX)PTCA GUIDING CATHETER 6F CLS 3.0.Should be FDA\"/CE\"/DCGI approved |
| 329 | (EX)PTCA GUIDING CATHETER 7F CLS 3.0.Should be FDA\"/CE\"/DCGI approved |
| 330 | (EX)PTCA GUIDING CATHETER 8F CLS 3.0.Should be FDA\"/CE\"/DCGI approved |
| 331 | (EX)PTCA GUIDING CATHETER 4F CLS 3.5.Should be FDA\"/CE\"/DCGI approved |
| 332 | (EX)PTCA GUIDING CATHETER 5F CLS 3.5Should be FDA\"/CE\"/DCGI approved |
| 333 | (EX)PTCA GUIDING CATHETER 6F CLS 3.5.Should be FDA\"/CE\"/DCGI approved |
| 334 | (EX)PTCA GUIDING CATHETER 7F CLS 3.5.Should be FDA\"/CE\"/DCGI approved |
| 335 | (EX)PTCA GUIDING CATHETER 8F CLS 3.5.Should be FDA\"/CE\"/DCGI approved |
| 336 | (EX)PTCA GUIDING CATHETER 4F AL 0.75.Should be FDA\"/CE\"/DCGI approved |
| 337 | (EX)PTCA GUIDING CATHETER 5F AL 0.75Should be FDA\"/CE\"/DCGI approved |
| 338 | (EX)PTCA GUIDING CATHETER 6F AL 0.75.Should be FDA\"/CE\"/DCGI approved |
| 339 | (EX)PTCA GUIDING CATHETER 7F AL 0.75.Should be FDA\"/CE\"/DCGI approved |
| 340 | (EX)PTCA GUIDING CATHETER 8F AL 0.75.Should be FDA\"/CE\"/DCGI approved |
| 341 | (EX)PTCA GUIDING CATHETER 4F AL 1.0.Should be FDA\"/CE\"/DCGI approved |
| 342 | (EX)PTCA GUIDING CATHETER 5F AL 1.0Should be FDA\"/CE\"/DCGI approved |
| 343 | (EX)PTCA GUIDING CATHETER 6F AL 1.0.Should be FDA\"/CE\"/DCGI approved |
| 344 | (EX)PTCA GUIDING CATHETER 7F AL 1.0.Should be FDA\"/CE\"/DCGI approved |
| 345 | (EX)PTCA GUIDING CATHETER 8F AL 1.0.Should be FDA\"/CE\"/DCGI approved |
| 346 | (EX)PTCA GUIDING CATHETER 4F AL 1.5.Should be FDA\"/CE\"/DCGI approved |
| 347 | (EX)PTCA GUIDING CATHETER 5F AL 1.5.Should be FDA\"/CE\"/DCGI approved |
| 348 | (EX)PTCA GUIDING CATHETER 6F AL 1.5.Should be FDA\"/CE\"/DCGI approved |
| 349 | (EX)PTCA GUIDING CATHETER 7F AL 1.5.Should be FDA\"/CE\"/DCGI approved |
| 350 | (EX)PTCA GUIDING CATHETER 8F AL 1.5.Should be FDA\"/CE\"/DCGI approved |
| 351 | (EX)PTCA GUIDING CATHETER 4F AL 2.0.Should be FDA\"/CE\"/DCGI approved |
| 352 | (EX)PTCA GUIDING CATHETER 5F AL 2.0.Should be FDA\"/CE\"/DCGI approved |
| 353 | (EX)PTCA GUIDING CATHETER 6F AL 2.0.Should be FDA\"/CE\"/DCGI approved |
| 354 | (EX)PTCA GUIDING CATHETER 7F AL 2.0.Should be FDA\"/CE\"/DCGI approved |
| 355 | (EX)PTCA GUIDING CATHETER 8F AL 2.0.Should be FDA\"/CE\"/DCGI approved |
| 356 | (EX)PTCA GUIDING CATHETER 4F AR 1.0.Should be FDA\"/CE\"/DCGI approved |
| 357 | (EX)PTCA GUIDING CATHETER 5F AR 1.0.Should be FDA\"/CE\"/DCGI approved |
| 358 | (EX)PTCA GUIDING CATHETER 6F AR 1.0.Should be FDA\"/CE\"/DCGI approved |
| 359 | (EX)PTCA GUIDING CATHETER 7F AR 1.0.Should be FDA\"/CE\"/DCGI approved |
| 360 | (EX)PTCA GUIDING CATHETER 8F AR 1.0.Should be FDA\"/CE\"/DCGI approved |
| 361 | (EX)PTCA GUIDING CATHETER 4F AR 2.0.Should be FDA\"/CE\"/DCGI approved |
| 362 | (EX)PTCA GUIDING CATHETER 5F AR 2.0.Should be FDA\"/CE\"/DCGI approved |
| 363 | (EX)PTCA GUIDING CATHETER 6F AR 2.0.Should be FDA\"/CE\"/DCGI approved |
| 364 | (EX)PTCA GUIDING CATHETER 7F AR 2.0.Should be FDA\"/CE\"/DCGI approved |
| 365 | (EX)PTCA GUIDING CATHETER 8F AR 2.0.Should be FDA\"/CE\"/DCGI approved |
| 366 | (EX) 6F 3D RDC GUIDING CATHETER .Should be FDA\"/CE\"/DCGI approved |
| 367 | (EX) 7F 3D RDC GUIDING CATHETER .Should be FDA\"/CE\"/DCGI approved |
| 368 | (EX) 4F RADIAL TIG 4.0 PTCA GUIDING CATHETER.Should be FDA\"/CE\"/DCGI approved |
| 369 | (EX) 5F RADIAL TIG 4.0 PTCA GUIDING CATHETER.Should be FDA\"/CE\"/DCGI approved |
| 370 | (EX) 6F RADIAL TIG 4.0 PTCA GUIDING CATHETER.Should be FDA\"/CE\"/DCGI approved |
| 371 | (EX) 7F RADIAL TIG 4.0 PTCA GUIDING CATHETER.Should be FDA\"/CE\"/DCGI approved |
| 372 | (EX) 4F RADIAL TIG 4.5 PTCA GUIDING CATHETER.Should be FDA\"/CE\"/DCGI approved |
| 373 | (EX) 5F RADIAL TIG 4.5 PTCA GUIDING CATHETER.Should be FDA\"/CE\"/DCGI approved |
| 374 | (EX) 6F RADIAL TIG 4.5 PTCA GUIDING CATHETER.Should be FDA\"/CE\"/DCGI approved |
| 375 | (EX) 7F RADIAL TIG 4.5 PTCA GUIDING CATHETER.Should be FDA\"/CE\"/DCGI approved |
| 376 | (EX) 4F IKARI LEFT 3.5 PTCA GUIDING CATHETER.Should be FDA\"/CE\"/DCGI approved |
| 377 | (EX) 5F IKARI LEFT 3.5 PTCA GUIDING CATHETER.Should be FDA\"/CE\"/DCGI approved |
| 378 | (EX) 6F IKARI LEFT 3.5 PTCA GUIDING CATHETER.Should be FDA\"/CE\"/DCGI approved |
| 379 | (EX) 7F IKARI LEFT 3.5 PTCA GUIDING CATHETER.Should be FDA\"/CE\"/DCGI approved |
| 380 | (EX) 4F IKARI LEFT 3.75 PTCA GUIDING CATHETER.Should be FDA\"/CE\"/DCGI approved |
| 381 | (EX) 5F IKARI LEFT 3.75 PTCA GUIDING CATHETER.Should be FDA\"/CE\"/DCGI approved |
| 382 | (EX) 6F IKARI LEFT 3.75 PTCA GUIDING CATHETER.Should be FDA\"/CE\"/DCGI approved |
| 383 | (EX) 7F IKARI LEFT 3.75 PTCA GUIDING CATHETER.Should be FDA\"/CE\"/DCGI approved |
| 384 | (EX) 4F IKARI LEFT 4.0 PTCA GUIDING CATHETER.Should be FDA\"/CE\"/DCGI approved |
| 385 | (EX) 5F IKARI LEFT 4.0 PTCA GUIDING CATHETER.Should be FDA\"/CE\"/DCGI approved |
| 386 | (EX) 6F IKARI LEFT 4.0 PTCA GUIDING CATHETER.Should be FDA\"/CE\"/DCGI approved |
| 387 | (EX) 7F IKARI LEFT 4.0 PTCA GUIDING CATHETER.Should be FDA\"/CE\"/DCGI approved |
| 388 | (EX) 4F IKARI LEFT 4.5 PTCA GUIDING CATHETER.Should be FDA\"/CE\"/DCGI approved |
| 389 | (EX) 5F IKARI LEFT 4.5 PTCA GUIDING CATHETER.Should be FDA\"/CE\"/DCGI approved |
| 390 | (EX) 6F IKARI LEFT 4.5 PTCA GUIDING CATHETER.Should be FDA\"/CE\"/DCGI approved |
| 391 | (EX) 7F IKARI LEFT 4.5 PTCA GUIDING CATHETER.Should be FDA\"/CE\"/DCGI approved |
| 392 | (EX) 4F IKARI RIGHT 1.0 PTCA GUIDING CATHETER.Should be FDA\"/CE\"/DCGI approved |
| 393 | (EX) 5F IKARI RIGHT 1.0 PTCA GUIDING CATHETER.Should be FDA\"/CE\"/DCGI approved |
| 394 | (EX) 6F IKARI RIGHT 1.0 PTCA GUIDING CATHETER.Should be FDA\"/CE\"/DCGI approved |
| 395 | (EX) 7F IKARI RIGHT 1.0 PTCA GUIDING CATHETER.Should be FDA\"/CE\"/DCGI approved |
| 396 | (EX) 4F IKARI RIGHT 1.5 PTCA GUIDING CATHETER.Should be FDA\"/CE\"/DCGI approved |
| 397 | (EX) 5F IKARI RIGHT 1.5 PTCA GUIDING CATHETER.Should be FDA\"/CE\"/DCGI approved |
| 398 | (EX) 6F IKARI RIGHT 1.5 PTCA GUIDING CATHETER.Should be FDA\"/CE\"/DCGI approved |
| 399 | (EX) 7F IKARI RIGHT 1.5 PTCA GUIDING CATHETER.Should be FDA\"/CE\"/DCGI approved |
| 400 | (EX) 4F IKARI RIGHT 2.0 PTCA GUIDING CATHETER.Should be FDA\"/CE\"/DCGI approved |
| 401 | (EX) 5F IKARI RIGHT 2.0 PTCA GUIDING CATHETER.Should be FDA\"/CE\"/DCGI approved |
| 402 | (EX) 6F IKARI RIGHT 2.0 PTCA GUIDING CATHETER.Should be FDA\"/CE\"/DCGI approved |
| 403 | (EX) 7F IKARI RIGHT 2.0 PTCA GUIDING CATHETER.Should be FDA\"/CE\"/DCGI approved |
| 404 | (EX) 5F KIMMY PTCA GUIDING CATHETER.Should be FDA\"/CE\"/DCGI approved |
| 405 | (EX) 6F KIMMYPTCA GUIDING CATHETER.Should be FDA\"/CE\"/DCGI approved |
| 406 | (EX) 5F KIMMY MINOR PTCA GUIDING CATHETER.Should be FDA\"/CE\"/DCGI approved |
| 407 | (EX) 6F KIMMY MINOR PTCA GUIDING CATHETER.Should be FDA\"/CE\"/DCGI approved |
| 408 | (S)Sheathless PTCA guiding catheter for coronary interventions from radial access 5F. Should be FDA/CE/DGCI approved |
| 409 | (S)Sheathless PTCA guiding catheter for coronary interventions from radial access 6F. Should be FDA/CE/DGCI approved |
| 410 | (S)Sheathless PTCA guiding catheter for coronary interventions from radial access 7F. Should be FDA/CE/DGCI approved |
| 411 | (S)Sheathless PTCA guiding catheter for coronary interventions from radial access 8F. Should be FDA/CE/DGCI approved |
| 412 | (S)Coronary guide extension catheter 8 Fr .Should be FDA\"/CE\"/DCGI approved |
| 413 | (S)Coronary guide extension catheter with distal 2 mm radioluscent tip capable of doing OCT in coronary ostial lesion.Should be FDA\"/CE\"/DCGI approved |
| 414 | ( S)Superselective cathether for Mother and Child technique.Should be FDA\" or CE\" and DCGI approved |
| 415 | (S)Coronary Guide Extension Catheter 6Fr. Should be FDA\"/CE\"/DCGI approved |
| 416 | (S)Coronary Guide Extension Catheter 7Fr. Should be FDA\"/CE\"/DCGI approved |
| 417 | (S)Soft Guideliner system for mother and child technique. Should be FDA\" or CE\" and DCGI approved |
| 418 | CORONARY WIRES |
| 419 | (S)PTCA WIRES Floppy standard length .Should be FDA\"/CE\"/DCGI approved |
| 420 | (S)PTCA WIRES Floppy extra supportexchange length.Should be FDA\"/CE\"/DCGI approved |
| 421 | (S)PTCA WIRES Floppy extra supportIntermediate Standard Length.Should be FDA\"/CE\"/DCGI approved |
| 422 | (S)PTCA WIRES Floppy Extra support Standard Length.Should be FDA\"/CE\"/DCGI approved |
| 423 | (S)PTCA DOC LINK EXTENSION Floppy extra supportWIRES.Should be FDA\"/CE\"/DCGI approved |
| 424 | (S)Floppy extra support EXCHANGE WIRES FOR PTCA .Should be FDA\"/CE\"/DCGI approved |
| 425 | (S)Double core spring tip core to tip Floppy extra support TYPE WIRES FOR PTCA.Should be FDA\"/CE\"/DCGI approved |
| 426 | (S)PTCA WIRES Floppy extra supportTapering Tip Hydrophilic.Should be FDA\"/CE\"/DCGI approved |
| 427 | (S)PTCA WIRE - Floppy extra support CTO WIRES-PLATINUM.Should be FDA\"/CE\"/DCGI approved |
| 428 | (S)PTCA WIRES CTO- hydrophobicFloppy extra support.Should be FDA\"/CE\"/DCGI approved |
| 429 | (S)PTCA WIRES for CTO-hydrophlic without polymer coatingFloppy extra supportExtra support.Should be FDA\"/CE\"/DCGI approved |
| 430 | (S)PTCA WIRES Polymer Coated Hydrophilic Floppy extra support .Should be FDA\"/CE\"/DCGI approved |
| 431 | (S)PTCA WIRES Polymer Coated Hydrophilic Floppy Extra support.Should be FDA\"/CE\"/DCGI approved |
| 432 | (S)PTCA WIRES- Polymer coated Floppy extra support tapering tip.Should be FDA\"/CE\"/DCGI approved |
| 433 | (S)PTCA WIRES - Specially Designed Floppy extra supportfor Tortuous vessels.Should be FDA\"/CE\"/DCGI approved |
| 434 | (S)PTCA WIRES Floppy extra support Hybrid coated.Should be FDA\"/CE\"/DCGI approved |
| 435 | (S)PTCA WIRES Floppy extra support Extrasupport Polymer coated.Should be FDA\"/CE\"/DCGI approved |
| 436 | (S)LINK EXTENSION Floppy extra support PTCA wire type 300 cm wires.Should be FDA\"/CE\"/DCGI approved |
| 437 | (S)PTCA 009 exchange length floppy wires for Retrograde approach exchange length.Should be FDA\"/CE\"/DCGI approved |
| 438 | (S)PTCA wire for CTO hydrophobic straight with tip loads available upto 12 gm.Should be FDA\"/CE\"/DCGI approved |
| 439 | (S)PTCA wire for collateral crossing with tip load of 0.3 gm.Should be FDA\"/CE\"/DCGI approved |
| 440 | (S)PTCA wire for CTO hydrophilic with a uncoated distal tip, preshaped.Should be FDA\"/CE\"/DCGI approved |
| 441 | (S)PTCA 009 exchange length floppy extra support wires for Retrograde approach exchange length.Should be FDA\"/CE\"/DCGI approved |
| 442 | CORONARY BALLOONS |
| 443 | (S) (EX)Rapid Exchange BalloonSystems with Semi-Compliant Design with Excellent Trackability and High Inflation Pressures all sizes.Should be FDA andDCGI approved |
| 444 | (S) (EX)Rapid Exchange BalloonSystems with Compliant Design with Excellent Trackability and High Inflation Pressures all sizes .Should be FDA andDCGI approved |
| 445 | (S) (EX)Rapid Exchange BalloonSystems with short overhang and Semi-Compliant Design with Excellent Trackability and High Inflation Pressures all sizes .Should be CE\" andDCGI approved |
| 446 | (S) (EX)Rapid Exchange BalloonSystems with short overhang Compliant Design with Excellent Trackability and High Inflation Pressures all sizes .Should be CE\" andDCGI approved |
| 447 | (S) (EX)Rapid Exchange BalloonSystems Low profile with Semi-Compliant Design with Excellent Trackability and High Inflation Pressures all sizes.Should be FDA andDCGI approved |
| 448 | (S) (EX)Rapid Exchange BalloonSystems with low profile Compliant Design with Excellent Trackability and High Inflation Pressures all sizes .Should be FDA andDCGI approved |
| 449 | (S) (EX)Rapid Exchange Non-Compliant Balloons for PTCA of fibroticlesions all sizes.Should be FDA and DCGI approved |
| 450 | (S) (EX)Rapid Exchange Non-Compliant Balloons for PTCA of calcific lesions all sizes.Should be FDA and DCGI approved |
| 451 | (S) (EX)Rapid Exchange Non-Compliant Balloons for PTCA of fibrotic lesions with short overhang all sizes.Should be FDA and DCGI approved |
| 452 | (S) (EX)Rapid Exchange Non-Compliant Balloons for PTCA of calcific lesions with short overhangall sizes.Should be FDA and DCGI approved |
| 453 | (S) (EX)Rapid Exchange Non-Compliant Balloons Low profile for PTCA of fibroticlesions all sizes.Should be FDA and DCGI approved |
| 454 | (S) (EX)Rapid Exchange Non-Compliant Balloons Low profile for PTCA of calcific lesions all sizes.Should be FDA and DCGI approved |
| 455 | (S) (EX)Rapid Exchange Non-Compliant High-Pressure Balloons for PTCA all sizes.Should be FDA and DCGI approved |
| 456 | (S) (EX)Rapid Exchange Non-Compliant Ultrahigh pressure balloon for calcific lesions (30 atm and above for PTCA) all sizes .Should be FDA and DCGI approved |
| 457 | (S) (EX)Rapid Exchange Non-Compliant nominal pressure balloon for CTO intervention of all sizes.Should be FDA and DCGI approved |
| 458 | (S) (EX)Rapid Exchange Non-Compliant high pressure balloon for CTO intervention all sizes.Should be FDA and DCGI approved |
| 459 | (S) (EX)Rapid Exchange Non-Compliant Ultrahigh pressure balloon for CTO intervention all sizes.Should be FDA and DCGI approved |
| 460 | (S) (EX) Rapid Exchange Non-Compliant Balloons for PTCA all sizes.Should be CE\" andDCGI approved |
| 461 | (S) (EX)Rapid Exchange ULTRA HIGH PRESSURE (upto 35atm) Non-Compliant Balloons for PTCA.Should be FDA and DCGI approved |
| 462 | (S) (EX) Rapid Exchange ULTRA HIGH PRESSURE (upto 45atm)Non-Compliant Balloons for PTCA.Should be CE\" andDCGI approved |
| 463 | (S)( EX)Ultra low profile Non compliant balloons for PCI.Should be CE\" AND DCGI approved |
| 464 | (S)( EX)Ultra low profile compliant balloons for PCI.Should be CE\" AND DCGI approved |
| 465 | (S)( EX)Ultra low profile semi complaint baloons for PCI.Should be CE\" AND DCGI approved |
| 466 | (S)( EX)low profile CTO baloons for PCI0.65mm in diameter.Should be CE\" AND DCGI approved |
| 467 | (S)( EX)low profile CTO baloons for PCI0.75mm in diameter.Should be CE\" AND DCGI approved |
| 468 | (S) (EX)Over the wire Balloons for PTCA compliant .Should be FDA\" OR CE\" AND DCGI approved |
| 469 | (S) (EX)Over the wire Balloons for PTCA Semicompliant .Should be FDA\" OR CE\" AND DCGI approved |
| 470 | (S) (EX)Over the wire Balloons for PTCA Semicompliant for CTO .Should be FDA\" OR CE\" AND DCGI approved |
| 471 | (S) (EX)Over the wire Balloons for PTCA Non-compliant .Should be FDA\" OR CE\" AND DCGI approved |
| 472 | (S) (EX)Over the wire Balloons for PTCA Noncompliant for CTO .Should be FDA\" OR CE\" AND DCGI approved |
| 473 | (S)(EX)Over the wire Balloons for PTSMA.Should be FDA\" OR CE\" AND DCGI approved |
| 474 | (S)( EX)Cutting Balloons Coronary.Should be FDA\" OR CE\" AND DCGI approved |
| 475 | (S)(EX) Scoring Coronary BalloonsFor severely calcified lesions.Should be FDA\" OR CE\" AND DCGI approved |
| 476 | (S) (EX)Drug elutingCoronary Balloons for in stent restenosis Coronary PACLITAXEL ELUTING Should be FDA\" OR CE\" AND DCGI approved |
| 477 | (S) ( EX) Dedicated non compliant coronary balloon for proximal optimisation technique(POT balloon)with shoulder length of 0.6 mm or less. Should be FDA\"/CE\"/DCGI approved |
| 478 | (S) ( EX) Coronary perfusion balloon catheter.Should be FDA\"/CE\"/DCGI approved |
| 479 | (S) (EX)Drug elutingCoronary Balloons for in stent restenosis Coronary SIROLIMUSELUTING Should be FDA\" OR CE\" AND DCGI approved |
| 480 | CORONARY STENTS |
| 481 | (S)(EX)Balloon expandableBARE METALCobalt chromium alloy CORONARY STENTS .Should be FDA\" OR CE\" AND DCGI approved |
| 482 | (S)(EX) Balloon expandable sirolimus eluting second generation coronary stents.Should be FDA\" OR CE\" AND DCGI approved |
| 483 | (S)(EX)Balloon expadable everolimus eluting second generation coronary stents.Should be FDA\" OR CE\" AND DCGI approved |
| 484 | (S)(EX)Balloon expadable zoratolimus eluting second generation coronary stents.Should be FDA\" OR CE\" AND DCGI approved |
| 485 | (S)(EX)Balloon expadable sirolimus eluting third generation coronary stents.Should be FDA\" OR CE\" AND DCGI approved |
| 486 | (S)(EX)Balloon expadable everolimus eluting third generation coronary stents.Should be FDA\" OR CE\" AND DCGI approved |
| 487 | (S)(EX)Balloon expadable zotarolimus eluting third generation coronary stents.Should be FDA\" OR CE\" AND DCGI approved |
| 488 | (S)(EX)Balloon expandableSirolimuscoatedCobalt chromium alloy LESS than 70micrometer strutCORONARY STENTS .Should be FDA\" OR CE\" AND DCGI approved |
| 489 | (S)(EX)Balloon expandableSirolimuscoatedCobalt chromium alloy MORE than 70micrometer strut CORONARY STENTS .Should be FDA\" OR CE\" AND DCGI approved |
| 490 | (S)(EX)Balloon expandableEverolimuscoatedCobalt chromium alloy LESS than 70micrometer strutCORONARY STENTS .Should be FDA\" OR CE\" AND DCGI approved |
| 491 | (S)(EX)Balloon expandableEverolimuscoatedCobalt chromium alloy MOREthan 70micrometer strutCORONARY STENTS .Should be FDA\" OR CE\" AND DCGI approved |
| 492 | (S)(EX)Balloon expandableZotarolimuscoatedCobalt chromium alloy LESS than 70micrometer strutCORONARY STENTS .Should be FDA\" OR CE\" AND DCGI approved |
| 493 | (S)(EX)Balloon expandableZotarolimuscoatedCobalt chromium alloy MORE than 70micrometer strutCORONARY STENTS .Should be FDA\" OR CE\" AND DCGI approved |
| 494 | (S)(EX)Balloon expandableBiolimuscoatedCobalt chromium alloy LESS than 70micrometer strutCORONARY STENTS .Should be FDA\" OR CE\" AND DCGI approved |
| 495 | (S)(EX)Balloon expandableBiolimuscoatedCobalt chromium alloy MOREthan 70micrometer strutCORONARY STENTS .Should be FDA\" OR CE\" AND DCGI approved |
| 496 | (S)(EX)Balloon expandableSirolimuscoatedPlatinum chromium alloy CORONARY STENTS .Should be FDA\" OR CE\" AND DCGI approved |
| 497 | (S)(EX)Balloon expandableEverolimuscoatedPlatinum chromium alloy CORONARY STENTS .Should be FDA\" OR CE\" AND DCGI approved |
| 498 | (S)(EX)Balloon expandableZotarolimuscoatedPlatinum chromium alloy CORONARY STENTS .Should be FDA\" OR CE\" AND DCGI approved |
| 499 | (S)(EX)Balloon expandableBiolimuscoatedPlatinum chromium alloy CORONARY STENTS .Should be FDA\" OR CE\" AND DCGI approved |
| 500 | (S)(EX)Balloon expandableSirolimuscoatedPlatinum iridium alloy CORONARY STENTS .Should be FDA\" OR CE\" AND DCGI approved |
| 501 | (S)(EX)Balloon expandableEverolimuscoatedPlatinum iridium alloy CORONARY STENTS .Should be FDA\" OR CE\" AND DCGI approved |
| 502 | (S)(EX)Balloon expandableZotarolimuscoatedPlatinum iridium alloy CORONARY STENTS .Should be FDA\" OR CE\" AND DCGI approved |
| 503 | (S)(EX)Balloon expandableBiolimuscoatedPlatinum iridium alloy CORONARY STENTS .Should be FDA\" OR CE\" AND DCGI approved |
| 504 | (S)(EX)Balloon expandableSirolimuscoatedPolymer free CORONARY STENTS .Should be FDA\" OR CE\" AND DCGI approved |
| 505 | (S)(EX)Balloon expandableEverolimuscoatedPolymer freeCORONARY STENTS .Should be FDA\" OR CE\" AND DCGI approved |
| 506 | (S)(EX)Balloon expandableZotarolimuscoatedPolymer freeCORONARY STENTS .Should be FDA\" OR CE\" AND DCGI approved |
| 507 | (S)(EX)Balloon expandableBiolimuscoatedPolymer free CORONARY STENTS .Should be FDA\" OR CE\" AND DCGI approved |
| 508 | (S)(EX)Balloon expandableSirolimuscoatedBiodegradable polymer CORONARY STENTS .Should be FDA\" OR CE\" AND DCGI approved |
| 509 | (S)(EX)Balloon expandableEverolimuscoatedBiodegradable polymer CORONARY STENTS .Should be FDA\" OR CE\" AND DCGI approved |
| 510 | (S)(EX)Balloon expandableZotarolimuscoatedBiodegradable polymer CORONARY STENTS .Should be FDA\" OR CE\" AND DCGI approved |
| 511 | (S)(EX)Balloon expandableBiolimuscoatedBiodegradable polymer CORONARY STENTS .Should be FDA\" OR CE\" AND DCGI approved |
| 512 | (S)(EX)DRUG ELUTING STENTS CEand DCGI APPROVED.Should be CE\" and DCGI approved |
| 513 | (S)(EX)DRUG ELUTING STENTS DCGI APPROVED.Should be DCGI approved |
| 514 | (S)(EX)DRUG ELUTING CORONARY STENTS TAPERING.Should be FDA\" OR CE\" AND DCGI approved |
| 515 | (S)(EX) DRUG ELUTING CORONARY STENTS EXTRA LENGTH ( beyond 38mm).Should be FDA\" OR CE\" AND DCGI approved |
| 516 | (S)(EX)DRUG ELUTING STENTS- POLYMER FREE.Should be FDA\" OR CE\" AND DCGI approved |
| 517 | (S)(EX)DRUG ELUTING STENTS- sizes above 48mm for diffuse lesions.Should be FDA\" OR CE\" AND DCGI approved |
| 518 | (S)(EX)DRUG ELUTING CORONARY STENTS 4 and 4.5mm diamater expandable at least to5.75 all lengths.Should be FDA\" OR CE\" AND DCGI approved |
| 519 | (S)(EX)Drug eluting stent mounted on drug coated balloon.Should be FDA\"/CE\"/DCGI approved |
| 520 | (S)(EX)Drug eluting bioresorbable vascular scaffold system for coronaries.Should be FDA\"/CE\"/DCGI approved |
| 521 | (S)(EX)COVERED STENTS-CORONARY Cobalt Chromium 5F guiding compatible Low profile all sizes.Should be FDA\"/CE\"/DCGI approved |
| 522 | (S)(EX)COVERED STENTS-CORONARY Cobalt Chromium6F guiding compatible Low profile all sizes.Should be FDA\"/CE\"/DCGI approved |
| 523 | (S)(EX)COVERED STENTS-CORONARY Stainless Steel6F guiding compatible Low profile all sizes.Should be FDA\"/CE\"/DCGI approved |
| 524 | (S)(EX)COVERED STENTS-CORONARY Stainless steel7F guiding compatible Low profile all sizes.Should be FDA\"/CE\"/DCGI approved |
| 525 | THROMBUS EXTRACTION |
| 526 | (S)(EX)Thrombus Extraction Catheters for Primary PTCA without stillette.Should be FDA\"/CE\"/DCGI approved |
| 527 | (S)(EX)Thrombus Extraction Catheters for coronary thrombus extraction floppy soft tip without stillette.Should be FDA\"/CE\"/DCGI approved |
| 528 | (S)(EX)Thrombus Extraction Catheters for Primary PTCA with stillette .Should be FDA\"/CE\"/DCGI approved |
| 529 | (S)(EX)Thrombus Extraction Catheters for Primary PTCA without stillette.Should be FDA\"/CE\"/DCGI approved |
| 530 | (S)(EX)Thrombus Extraction Catheters for Peripheral venous /Pulmonary thrombi 8F with a suction device provided by the company on demand .Should be FDA\"/CE\"/DCGI approved |
| 531 | (S)(EX)Thrombus Extraction Catheters for Peripheral arterial-venous thrombi 6F with a suction device provided by the company on demand .Should be FDA\"/CE\"/DCGI approved |
| 532 | (S)(EX)Thrombus Extraction Catheters for Peripheral arterial thrombi4F with a suction device provided by the company on demand .Should be FDA\"/CE\"/DCGI approved |
| 533 | MICROCATHETER |
| 534 | ( D) Coronary Microcatheters( 0.014\" compatable) with distal entry profile 1.8F.Should be FDA\" or CE\" andDCGI approved |
| 535 | ( D) Coronary Microcatheters( 0.014\" compatable) with distal entry profile 1.8F floppy tip .Should be FDA\" or CE\" andDCGI approved |
| 536 | ( D) Coronary Microcatheters( 0.014\" compatable) with distal entry profile 1.4F.Should be FDA\" or CE\" andDCGI approved |
| 537 | ( D) Coronary Microcatheters( 0.014\" compatable) with distal entry profile 1.4F Floppy tip.Should be FDA\" or CE\" andDCGI approved |
| 538 | ( D) Coronary Microcatheters for CTO entry- braided with cutting tip.Should be FDA\" or CE\" andDCGI approved |
| 539 | ( D) Coronary Microcatheters torquable ( 0.014\" compatable).Should be FDA\" or CE\" andDCGI approved |
| 540 | ( D)Dual lumen Coronarymicroguide catheters for sidebranch entry(over the wire and monorail).Should be FDA\" or CE\" and DCGI approved |
| 541 | (D)Angled tip coronary microcatheter for side branch access.Should be FDA\" or CE\" andDCGI approved |
| 542 | (D)Retrograde coronary collateral Channel dilator .Should be FDA\" or CE\" and DCGI approved |
| 543 | ( D) Peripheral Micro catheters for visceral angio embolisation-Should be hydrophilic and 0.021\" compatable.Should be FDA\" OR CE\" AND DCGI approved |
| 544 | ( D) Peripheral Micro catheters for visceral angio embolisation-Should be hydrophilic with attached 0.018\" hydrophilic wire.Should be FDA\" OR CE\" AND DCGI approved |
| 545 | IMAGING & PHYSIOLOGY |
| 546 | (D) Intravascular Ultrasound Catheters compatiblewith Volcano IVUS system .Should be FDA\"/CE\"/DCGI approved |
| 547 | (D) Intravascular Ultrasound Catheters compatiblewith ILAB IVUS system with Pull back Sled.Should be FDA\"/CE\"/DCGI approved |
| 548 | (D) Intravascular Ultrasound Catheters compatible with ILAB IVUS system.Should be FDA\"/CE\"/DCGI approved |
| 549 | (D)OCT Catheters .Should be FDA\"/CE\"/DCGI approved |
| 550 | (D)FFR WIRES compatible with Abbott FFR systems.Should be FDA\"/CE\"/DCGI approved |
| 551 | (D)FFR WIRES wireless, compatible with Abbott FFR systems.Should be FDA\"/CE\"/DCGI approved |
| 552 | (D) FFR WIRES compatible with Volcano FFR system .Should be FDA\"/CE\"/DCGI approved |
| 553 | (D) FFR WIRE Compatible with Boston FFR system.Should be FDA\"/CE\"/DCGI approved |
| 554 | CTO PCI |
| 555 | (EX)Ultra low profile semi compliant coronary balloons for Chronic total occlusions.Should be FDA\"/CE\"/DCGI approved |
| 556 | (EX)Dissection re entry balloon for coronary CTO.Should be FDA\"/CE\"/DCGI approved |
| 557 | (EX)Sub intimal tracking device for CTO.Should be FDA\"/CE\"/DCGI approved |
| 558 | DEBULKING SYSTEMS CORONARY |
| 559 | ( D)Rotablator Wire 009 Floppy.Should be FDA\"/CE\"/DCGI approved |
| 560 | ( D)Rotablator Wire 009 Extra support .Should be FDA\"/CE\"/DCGI approved |
| 561 | (D) (EX) Rotational atherectomy Burrall sizes |
| 562 | (D) Rotational atherectomy advancer |
| 563 | (D) (EX) Rotational atherectomy Burr and Advancer system integrated all sizes |
| 564 | (D) (EX)Coronary orbital atherectomy system for calcified coronary lesions all sizes.Should be FDA\"/CE\"/DCGI approved |
| 565 | (D) (EX) Coronary Laser Atherectomy catheter for intervention in calcified coronaries all sizes.Should be CE\" AND DCGI approved |
| 566 | (D) (EX)CORONARY intravascular Lithrotripsy balloons for heavy calcified proximal vessel PCI all sizes.Should be CE\" AND DCGI approved |
| 567 | IABP |
| 568 | (D) (EX)Intra aortic balloon pump balloons small, medium and large SIZES compatible with Datascope IABP systems.Should be FDA\"/CE\"/DCGI approved. |
| 569 | (D)Helium with tank for IABP Machine Datascope model. |
| 570 | BALOON VALVULOPLASTY |
| 571 | (S)(EX)ALL SIZES OF PTMC Balloons- Reusable.Should be FDA\"/CE\"/DCGI approved |
| 572 | (S)Accessories for PTMC Balloons.Should beCE\" AND DCGI approved, the accessories will be procured from the same company is selected for PTMC balloons . Accessories include a) Coiled LA guide wire for tracking the balloon into LA b) 21F black dilatorc) LV entry wire d) metal stretching tube e) stylet f) syringe for inflation g) ruler/calliper for measuring balloon size |
| 573 | (D)(EX)ALL SIZES OF PTMC Balloons with Accessories- Reusable.Should be FDA\"/CE\"/DCGI approved |
| 574 | (D)(EX)All sizes of Mitral Valve Balloon Dilatation Systems with reusable latex rubber balloon design and accessories are to be quoted. Should be FDA\"/CE\"/DCGI approved |
| 575 | (D)(EX)All sizes of Mitral Valve Balloon Dilatation Systems with reusable latex rubber balloon design. Should be FDA\",CE\"/DCGI approved |
| 576 | (D)(EX) Accessories for Mitral Valve Balloon Dilatation Systems with reusable latex rubber balloon design . the accessories will be procured from the same company is selected for Mitral Valve Balloon Dilatation Systems with reusable latex rubber balloon design.a) Coiled LA guide wire for tracking the balloon into LA b) 21F black dilatorc) LV entry wire d) metal stretching tube e) stylet f) syringe for inflation g) ruler/calliper for measuring balloon size Should be FDA,CE\"/DCGI approved |
| 577 | (D)( EX) Aortic valvuloplasty balloon systems with accessories of all sizes and lengths.Should be FDA\"/CE\"/DCGI approved |
| 578 | (D)( EX)Pulmonary valvuloplasty balloon systems with accessories all sizs and lengths .Should be CE\"/DCGI approved |
| 579 | (D)( EX)Stepped diameter balloons Cribier- Letac with accessories all sizes and lengths.Should be FDA\"/CE\"/DCGI approved |
| 580 | (D)(EX)Pediatric Valvuloplasty Tyshak MINI 014 compatible balloons with accelerator, Bifoil balloons, Trifoil Balloons with accessories all sizes.Should be FDA\"/CE\"/DCGI approved |
| 581 | (D)(EX)Pediatric Valvuloplasty Tyshak-II balloons with accelerator, Bifoil balloons with accessories all sizes.Should be FDA\"/CE\"/DCGI approved |
| 582 | (D)(EX)Pediatric Valvuloplasty Tyshak-II balloons with accelerator, Trifoil Balloons with accessories all sizes.Should be FDA\"/CE\"/DCGI approved |
| 583 | (D) (EX)Low profile non-compliant pediatric valvuloplasty balloons 4-10 mm diameter, with introducer size starting at 4 Fr with accessories.Should be FDA\"/CE\"/DCGI approved |
| 584 | PERIPHERAL INTERVENTION |
| 585 | (S)BALKAN CONTRALATERAL SHEATH 6F.Should be FDA\"/CE\"/DCGI approved |
| 586 | (S)BALKAN CONTRALATERAL SHEATH 7F.Should be FDA\"/CE\"/DCGI approved |
| 587 | (S)BALKAN CONTRALATERAL SHEATH 8F.Should be FDA\"/CE\"/DCGI approved |
| 588 | (S)(EX)High pressure non compliant peripheral balloons- (sizes from 4mm-10mm) 0.035\"\" compatable (All lengths).Should be CE\" and DCGI approved |
| 589 | (S)( EX)Cutting Balloons Peripheral. 6mm to 8mm diamter all lengths Should be FDA\" OR CE\" AND DCGI approved |
| 590 | (S)(EX) Scoring Balloons - Peripheral- For severely calcified lesions.Should be FDA\" OR CE\" AND DCGI approved |
| 591 | (S)(EX)Drug Eluting Balloons Peripheral.Should be FDA\" OR CE\" AND DCGI approved |
| 592 | (S)(EX)Drug Eluting Balloons Peripheral for ISR .Should be FDA\" OR CE\" AND DCGI approved |
| 593 | (S) (EX)Ultra high pressure Mustang type balloons Peripheral- sizes from 4mm to 10mm all lengths..Should be FDA\" OR CE\" AND DCGI approved |
| 594 | (EX) Covered self expanding covered stent grafts for Peripheral anurysm and leaks (4mm to 12mm).Should be FDA\" or CE\" andDCGI approved |
| 595 | (S)LEFT INTERNAL MAMMARY GUIDE CATHETER5F, 6F and & 7F .Should be FDA\"/CE\"/DCGI approved |
| 596 | (S)BRAIDED MULTIPURPOSE GUIDE CATHS(5F AND 6F).Should be FDA\"/CE\"/DCGI approved |
| 597 | (S) SOFT TIPPED braided Guide catheters for (4F,5F) for coronary/visceral use.Should be FDA\" or CE\" and DCGI approved |
| 598 | (S)BRAIDED SIMMONS SHAPED CEREBRAL CATHS.Should be FDA\"/CE\"/DCGI approved |
| 599 | (S)RENAL DOUBLE CURVE GUIDE CATHETER 4F, 5F80CM , 120 CM, 140 CM.Should be FDA\"/CE\"/DCGI approved |
| 600 | (S)RENAL DOUBLE CURVE GUIDE CATHETER 4F, 5F80CM , 120 CM, 140 CM.Should be FDA\"/CE\"/DCGI approved |
| 601 | (S)RENAL DOUBLE CURVE GUIDE CATHETER 6F80CM , 120 CM, 140 CM.Should be FDA\"/CE\"/DCGI approved |
| 602 | (S)RENAL DOUBLE CURVE GUIDE CATHETER 7F80CM, 120 CM, 140 CM.Should be FDA\"/CE\"/DCGI approved |
| 603 | (S) TERUMO GLIDE CATHETER HEAD HUNTER 4F.Should be FDA\"/CE\"/DCGI approved |
| 604 | (S) TERUMO GLIDE CATHETERHEAD HUNTER 5F AND 6 F.Should be FDA\"/CE\"/DCGI approved |
| 605 | (S) TERUMO GLIDE CATHETER COBRA 4F.Should be FDA\"/CE\"/DCGI approved |
| 606 | (S) TERUMO GLIDE CATHETER 4F.Should be FDA\"/CE\"/DCGI approved |
| 607 | (S)YASHIRO GLIDE CATHETER5F 6F80 CM,120 CM, 140 CM.Should be FDA\"/CE\"/DCGI approved |
| 608 | (S)YASHIRO GLIDE CATHETER 4F80 CM,120 CM,140CM.Should be FDA\"/CE\"/DCGI approved |
| 609 | ( EX)PERIPHERAL BALLOONS(0.035\" compatable) for femoro popliteal and iliac lesions.Should be FDA\"/CE\"/DCGI approved |
| 610 | (S) Fogarty arterial embolectomy catheter 4&5F.Should be FDA\"/CE\"/DCGI approved |
| 611 | ( EX) RENAL BALLOON(0.014\" compatable).Should be FDA\"/CE\"/DCGI approved |
| 612 | (EX)CAROTID and BTK BALLOONS(0.014\" compatable) .Balloon Shaft length should be160 CMAND ABOVE.Should be FDA\"/CE\"/DCGI approved |
| 613 | (EX)SMALL VESSEL BALLOON( Diameters should be from 1mm to 4mm) All lengths.Should be FDA\"/CE\"/DCGI approved |
| 614 | (EX)PERIPH /RENAL/CAROTID GUIDING-100 cm and longer.Should be FDA\"/CE\"/DCGI approved |
| 615 | (EX)RENAL STENTS -0.014\" compatable Balloon Mounted Shaft Length 80 cm- All sizes.Should be FDA\"/CE\"/DCGI approved |
| 616 | (EX) Self expanding Femoro popliteal stents - all diameters.Should be FDA\"/CE\"/DCGI approved |
| 617 | (EX)Dilators of Coons type for serial vascular dilation for large access .Should be CE\" and DCGI approved |
| 618 | (EX) Balloon expandable STENTS PERIPHERAL- All sizes.Should be FDA\"/CE\"/DCGI approved |
| 619 | (EX) Self expanding Iliac stents - all diameters.Should be FDA\" or CE\" and DCGI approved |
| 620 | ( EX) CAROTID DISTAL PROTECTION DEVICES.Should be FDA\"/CE\"/DCGI approved |
| 621 | ( EX) CAROTID STENTS TAPERINGSelf Expanding.Should be FDA\"/CE\"/DCGI approved |
| 622 | ( EX)CAROTID STENTSStraight Self Expanding.Should be FDA\"/CE\"/DCGI approved |
| 623 | (EX)STENT GRAFTS FOR VISCERAL VASCULAR SYSTEM(Should be highy trackable,0.035\" compatable).Should be FDA\"/CE\"/DCGI approved |
| 624 | (S) (EX)Sizing BALLOONS for ASD/PDA.Should be FDA\"/CE\"/DCGI approved |
| 625 | (S)PERIPHERAL GUIDE WIRES& SPECIALITY WIRES Exchange Length ( 0.018\").Should be FDA\"/CE\"/DCGI approved |
| 626 | (S)PERIPHERAL GUIDE WIRES& SPECIALITY WIRES Exchange length(0.035\").Should be FDA\"/CE\"/DCGI approved |
| 627 | (S)ROAD RUNNER POLYMER COATED WIRE 035 staright and J.Should be FDA\"/CE\"/DCGI approved |
| 628 | Peripheral intravascular lithotripsy catheter for treating calcified lesions in peripheral arteries like illiac, femoral and popliteal artery.Should be FDA\"/CE\"/DCGI approved |
| 629 | Highly flexible kink resitant peripheral stents suitable for deploying in superficial femoral artery and poplliteal artery.Should be FDA\"/CE\"/DCGI approved |
| 630 | (S)PERIPHERAL CHRONIC TOTAL OCCLUSION WIRES 0.014, 0.0.35 diameter.Should be FDA\"/CE\"/DCGI approved |
| 631 | RENAL DENERVATION |
| 632 | Renal artery denervation catheter system for management of resistant hypertension. Should be FDA/CE/DGCI approved |
| 633 | EMBOLIZATION |
| 634 | (S)(EX)Cyanoacrylate glue for sealing coronary perforation.Should be FDA\"/CE\"/DCGI approved |
| 635 | (S)(EX)EMBOLISATION PARTICLES Poly Vinyl Alcohol all sizes.Should be FDA\"/CE\"/DCGI approved |
| 636 | (S) Lipoidol for embolization Should be FDA\"/CE\"/DCGI approved |
| 637 | (S)Super Absorbant Polymer Microspheres for Drug( Doxorubucin) Adsorption for TACE.Should be FDA\"/CE\"/DCGI approved |
| 638 | (S)Gelfoam (Powder or granule form) for Embolization.Should be FDA\"/CE\"/DCGI approved |
| 639 | (S)N-butyl cyanoacrylate GLUE for Embolization .Should be FDA\"/CE\"/DCGI approved |
| 640 | (S)(EX)MICROCATHETERS with Inbuilt hydrophilic wire for Peripheral Angiography and Particle /Coil delivery.Should be FDA\"/CE\"/DCGI approved |
| 641 | (S)(EX)MICROCATHETERS - STEERABLE/ SHAPABLE with Inbuilt hydrophilic wire for Peripheral Angiography and Particle /Coil delivery.Should be FDA\"/CE\"/DCGI approved |
| 642 | (S)GEL FOAM POWDER FOR ANGIO EMBOLISATION.Should be FDA\" or CE\" and DCGI approved |
| 643 | (EX) EMBOLIZATION COILS 035\" all sizes.Should be FDA\"/CE\"/DCGI approved |
| 644 | (EX) EMBOLIZATION COILS 0.038 to 052\" all sizes.Should be FDA\"/CE\"/DCGI approved |
| 645 | (EX) EMBOLIZATION COILS 052\" all sizes.Should be FDA\"/CE\"/DCGI approved |
| 646 | ( EX) EMBOLIZATION MICRO COILS 018 all sizes - Non Detachable and freely deliverable.Should be FDA\"/CE\"/DCGI approved |
| 647 | ( EX)EMBOLIZATION MICRO COILS 018 all sizes -DETACHABLE 2D.Should be FDA\"/CE\"/DCGI approved |
| 648 | ( S) EMBOLIZATION COILS Highly trackable 0.018\"\" embolisation coils for post op- visceral (GI and Renal artery pseudoaneurysm) .Should be CE\" AND DCGI approved |
| 649 | ( EX) EMBOLIZATION MICRO COILS 018 all sizes -DETACHABLE 3D.Should be FDA\"/CE\"/DCGI approved |
| 650 | (EX)Nitinol Vascular plugs for embolisation.Should be FDA\"/CE\"/DCGI approved |
| 651 | EX)Bi lobed Nitinol Vascular plugs for embolisation.Should be FDA\"/CE\"/DCGI approved |
| 652 | EX)Tri lobed ( should have retention disk on both sides)Nitinol Vascular plugs for embolisation.Should be FDA\"/CE\"/DCGI approved |
| 653 | EX)Nitinol Vascular plugs for embolisation deliverable through smallest Fr diagnostic catheter supporting 0.038 guidewire .Should be FDA\"/CE\"/DCGI approved |
| 654 | SNARES |
| 655 | (EX)ENDOVASCULAR SNARES with Metal Tip.Should be FDA\"/CE\"/DCGI approved |
| 656 | (EX)ENDOVASCULAR SNARES with Polymer Tip.Should be FDA\"/CE\"/DCGI approved |
| 657 | (EX)ENDOVASCULAR SNARES Gooseneck. Should be FDA\"/CE\"/DCGI approved |
| 658 | (EX)ENDOVASCULAR SNARES Needle Eye. Should be FDA\"/CE\"/DCGI approved |
| 659 | (S)Coronary micro snares.Should be CE\" and DCGI approved |
| 660 | (EX)ENDOVASCULAR SNARES Basket. Should be FDA\"/CE\"/DCGI approved |
| 661 | COARCTATION STENTING |
| 662 | (D)(EX)Bare AORTIC STENTS FOR Coarctation (Sizes should be above 20mm up to 40mm) - Baloon expandable design.Should be FDA\"/CE\"/DCGI approved |
| 663 | (D) (EX) Non pre-mounted bare aortic stents with semi-open cell design made of cobalt-chromium with specially designed links for non-foreshortening on balloon-dilatation with low crimping profile capable ofbeing deliverable through sheath sizes starting from 9F. |
| 664 | (D)(EX)Non pre-mounted ePTFE covered aortic stents with semi-open cell design made of cobalt-chromium with specially designed links for non-foreshortening on balloon-dilatation with low crimping profile capable ofbeing deliverable through sheath sizes starting from 12F or smaller.Capable of being expanded to sizes starting from 14 mm to more than or equal to 22 mm |
| 665 | (D)(EX)Non pre-mounted bare aortic stents with semi-open cell design made of cobalt-chromium with minimum foreshortening on balloon-dilatation with low crimping profile capable |
| 666 | (D)(EX)Non pre-mounted bare aortic stents with semi-open cell design made of cobalt-chromium with minimum foreshortening on balloon-dilatation with low crimping profile |
| 667 | (D)(EX) Premounted ePTFE covered stents made of cobalt-chromium made for aortic coarctation stenting with low foreshortening on dilatation capable of being expanded from 12 to 24 mm capable of being delivered through sheath sizes starting from 9 F |
| 668 | (D)(EX) Premounted ePTFE covered stents made of cobalt-chromium with low foreshortening on dilatation capable of being expanded from 5mm to 10 mm capable of being delivered through sheath sizes starting from 6F meant for use in peripheral vessels, renal artery, arteriovenous fistulas for dialysis etc |
| 669 | (D)(EX) Non-premounted bare aortic stents made of platinum-iridium capable of being expanded from 8mm to 24 mm capable of being delivered through sheath sizes starting from 9F meant for use in aorta |
| 670 | (D)(EX) Non-premounted PTFE covered aortic stents made of platinum-iridium capable of being expanded from 8mm to 24 mm capable of being delivered through sheath sizes starting from 12F meant for use in aorta |
| 671 | (D)(EX) Bare AORTIC STENTS FOR Coarctation (Sizes should be above 12 to 20 mm) - Baloon expandable design.Should be FDA\"/CE\"/DCGI approved |
| 672 | (D)(EX) Bare AORTIC STENTS FOR Coarctation (Sizes should be above 20mm up to 40mm) - Self-expanding design.Should be FDA & DCGI approved |
| 673 | (D)(EX) Bare AORTIC STENTS FOR Coarctation (Sizes should be above 12 to 20 mm) - Self expanding design.Should be FDA & DCGI approved |
| 674 | (D)(EX) Covered AORTIC stents (balloon expandable only) for aortic coarctation (Sizes from 12 to 30mm). Should beCE\" AND DCGI approved. |
| 675 | (D) (EX) Balloon in Balloon Stent Placement Catheter for aortic coarcation (Sizes from 12 to 30mm). Should beCE\" AND DCGI approved. |
| 676 | (D)(EX) Covered Mounted AORTIC stents (balloon expandable only) for aortic coarctation (Sizes from 12 to 30mn). Should beCE\" AND DCGI approved |
| 677 | DEVICE CLOSURE ACCESSORIES |
| 678 | (S)MULLINS SHEATH with Matching Dilator withsidearm 6Fall sizes.Should be FDA\"/CE\"/DCGI approved ( Length to be specified) |
| 679 | (S)MULLINS SHEATH with Matching Dilator withsidearm 7Fall sizes.Should be FDA\"/CE\"/DCGI approved ( Length to be specified) |
| 680 | (S)MULLINS SHEATH with Matching Dilator withsidearm 8Fall sizes.Should be FDA\"/CE\"/DCGI approved ( Length to be specified) |
| 681 | (S)MULLINS SHEATH with Matching Dilator withsidearm 9Fall sizes.Should be FDA\"/CE\"/DCGI approved ( Length to be specified) |
| 682 | (S)MULLINS SHEATH with Matching Dilator withsidearm 10Fall sizes.Should be FDA\"/CE\"/DCGI approved ( Length to be specified) |
| 683 | (S)MULLINS SHEATH with Matching Dilator withsidearm 11Fall sizes.Should be FDA\"/CE\"/DCGI approved ( Length to be specified) |
| 684 | (S)MULLINS SHEATH with Matching Dilator withsidearm 12Fall sizes.Should be FDA\"/CE\"/DCGI approved ( Length to be specified) |
| 685 | (S)MULLINS SHEATH with Matching Dilator withsidearm 14Fall sizes.Should be FDA\"/CE\"/DCGI approved ( Length to be specified) |
| 686 | (S)MULLINS SHEATH with Matching Dilator withsidearm 16Fall sizes.Should be FDA\"/CE\"/DCGI approved ( Length to be specified) |
| 687 | ( S) 5F Flexible delivery sheaths with steerable and deflectable introducer systems for ASD/VSD/PDA device closure .Should be FDA/ CE\" AND DCGI approved |
| 688 | ( S) 6FFlexible delivery sheaths with steerable and deflectable introducer systems for ASD/VSD/PDA device closure .Should be FDA/ CE\" AND DCGI approved |
| 689 | ( S) 8F Flexible delivery sheaths with steerable and deflectable introducer systems for ASD/VSD/PDA device closure .Should be FDA/ CE\" AND DCGI approved |
| 690 | ( S) 10F Flexible delivery sheaths with steerable and deflectable introducer systems for ASD/VSD/PDA device closure .Should be FDA/ CE\" AND DCGI approved |
| 691 | ( S) 12F Flexible delivery sheaths with steerable and deflectable introducer systems for ASD/VSD/PDA device closure .Should be FDA/ CE\" AND DCGI approved |
| 692 | ( S) 14F Flexible delivery sheaths with steerable and deflectable introducer systems for ASD/VSD/PDA device closure .Should be FDA/ CE\" AND DCGI approved |
| 693 | (EX) COOK SHEATHS (all sizes 6F-7F) with check flo valves) WITH ANGLED TIPS FOR ASD DEVICE DELIVERY.Should be FDA\" or CE\" and DCGI approved |
| 694 | (EX) COOK SHEATHS (all sizes 8F-9F) with check flo valves) WITH ANGLED TIPS FOR ASD DEVICE DELIVERY.Should be FDA\" or CE\" and DCGI approved |
| 695 | (EX) COOK SHEATHS (all sizes 10F-11F) with check flo valves) WITH ANGLED TIPS FOR ASD DEVICE DELIVERY.Should be FDA\" or CE\" and DCGI approved |
| 696 | (EX) COOK SHEATHS (all sizes 12F-13F) with check flo valves) WITH ANGLED TIPS FOR ASD DEVICE DELIVERY.Should be FDA\" or CE\" and DCGI approved |
| 697 | (EX) COOK SHEATHS (all sizes 14F-15F) with check flo valves) WITH ANGLED TIPS FOR ASD DEVICE DELIVERY.Should be FDA\" or CE\" and DCGI approved |
| 698 | (EX) COOK SHEATHS (all sizes 16F) with check flo valves) WITH ANGLED TIPS FOR ASD DEVICE DELIVERY.Should be FDA\" or CE\" and DCGI approved |
| 699 | (EX) Ultra compliant linear Sizing balloons with markers for ASD balloon sizing (18mm,24mm 34mm).Should be CE/DCGI approved |
| 700 | (EX)Haursdorf delivery sheaths for ASD device closure all sizes. Should be FDA\"/CE\"/DCGI approved |
| 701 | ATRIAL SEPTAL DEVICES |
| 702 | (EX)ASD DEVICES: Allcustomised sizes from 8mm to 50 mm.Should beFDA/CE\" AND DCGI approved ( Device only) |
| 703 | (EX) Delivery cable for ASD Device 5F/6F for sizes 8mm to 50mm (the cable will be procured from the same company who is selected as L1 in the category : \" ASD DEVICES: Allcustomised sizes from 8mm to 50 mm Should beFDA,CE\" AND DCGI approved\" as indicated in the row above |
| 704 | ((EX)ASD DEVICES: Allcustomised sizes from 8mm to 50 mm.Should beFDA/CE\" AND DCGI approved ( Device only) |
| 705 | (EX) Delivery cable for ASD DEVICES: Allcustomised sizes from 4 mm waist diameter onwards (the cable will be procured from the same company which is selected as L1 in the category \"ASD DEVICES: Allcustomised sizes from 8mm to 50 mm.Should beFDA & CE\" AND DCGI approved\" as indicated in the row above |
| 706 | (EX)ASD DEVICES Allcustomised sizes from 8mm to 50 mm with Delivery cable and delivery system ( loading sheath and long sheath for device delivery): All customised sizes from 8mm to 50 mm.Should beFDA/CE\" AND DCGI approved |
| 707 | (EX)ASD DEVICES Allcustomised sizes from 8mm to 50 mm with Delivery cable and delivery system ( loading sheath and long sheath for device delivery): All customised sizes from 8mm to 50 mm.Should beFDA &CE\" AND DCGI approved |
| 708 | (EX) Fenestrated ASD device for mutiple septal defects with cable and accesories All sizes.Should be FDA\"/CE\"/DCGI approved |
| 709 | (EX)ASD AMPLATZER TYPE SELF CENTRE DEVICES WITH ALL sizes from 8mm and above .Should be FDA approved |
| 710 | (EX) Atrial septal occluder(self-centering) for complex morphology with balloon-assisted delivery with cable and accesories.Should be FDA\" or CE\" andDCGI approved |
| 711 | (EX) PURPLE Recovery sheaths for embolised ASD devices-16 F and above size.Should be FDA approved |
| 712 | (EX) Large sized atrial septal occluders above 40mm size with delivery sheath and cables.Should beCE\" AND DCGI approved |
| 713 | (EX) Dual disc nitinol biocompatable layer coated secundum type atrial occluders (ALL SIZSES) with Pre assembled delivery system.Should be FDA\" or CE\" andDCGI approved |
| 714 | (EX)Cribriform multifenestrated septal occluder with a narrow waist -various sizes; disc diameters upto 40 mm meant for occlusion of multifenestrated ASDs. Should be FDA /CE/DGCI approved |
| 715 | (EX)Atrial flow regulator device with delivery cable and accesories.Should be FDA/CE/DGCI approved |
| 716 | (EX)Patent foramen ovale (PFO) closure device with delivery cable and accesories.Should be FDA/CE/DGCI approved |
| 717 | PDA DEVICES |
| 718 | (D)(EX)PDA OCCUSION DEVICE --ALL CUSTOMISABLE SIZES FROM 3MM TO 20MM WAIST SIZE .Should be FDA\"/CE\"/DCGI approved ( Device only) |
| 719 | (D)(EX) Delivery Cable for PDA Occlusion Device (the cable will be procured from the same company who is selected as L1 in the category\" PDA OCCUSION DEVICE --ALL CUSTOMISABLE SIZES FROM 3MM TO 20MM WAIST SIZE .Should be FDA\"/CE\"/DCGI approved\" |
| 720 | (EX)PDA OCCUSION DEVICE --ALL CUSTOMISABLE SIZES WITH FROM 4MM TO 20MM WAIST SIZE . 4x6 device should be deliverable by 5Fr delivery system.Should be FDA\"&CE\"/DCGI approved ( Device only) |
| 721 | (EX) Delivery Cable set for PDA occlusion device (the cable will be procured from the same company that is selected as L1 in the category\" PDA OCCLUSION DEVICE --ALL CUSTOMISABLE SIZES FROM 4MM TO 20MM WAIST SIZE. 4x6 device should be deliverable by 5Fr delivery system. Should be FDA\"&CE\"/DCGI approved\" |
| 722 | (EX)PDA OCCUSION DEVICE --ALL CUSTOMISABLE SIZES WITH FROM 3MM TO 20MM WAIST SIZE with Delivery Cable.Should be FDA\"/CE\"/DCGI approved |
| 723 | (EX)PDA OCCUSION DEVICE --ALL CUSTOMISABLE SIZES WITH FROM 3MM TO 20MM WAIST SIZE with Delivery Cable.Should be FDA\"&CE\"/DCGI approved |
| 724 | (EX)ADO-1 device with delivery cable for all morphology.Should be FDA\" or CE\" andDCGI approved |
| 725 | (EX) DUCT OCCLUSION DEVICE with DELIVERY SYSTEM NONTAPERINGSHEATHS with sidearm+INTRODUCER CABLE SET .Should be FDA\"/CE\"/DCGI approved |
| 726 | (EX)PDA OCCUSION DEVICE with Dual Discs of equal size and delivery cable.Should be FDA\" or CE\" andDCGI approved |
| 727 | (EX)PDA DELIVERY SYSTEMS AND INTRODUCER CABLE SYSTEMS .Should be FDA\"/CE\"/DCGI approved. |
| 728 | (EX) Low profile Duct occluder device for neonates and infantswith delivery cable and 4F delivery systems. Should beFDA/CE\" AND DCGI approved |
| 729 | (EX) Low profile Duct occluder device for neonates compatible with 4F delivery system.Should be FDA CE\" AND DCGI approved ( Device Only) |
| 730 | (D)Delivery cable AND 4F sheath (the cable and sheath will be procured from the same company who is selected as L1 in the category\"Low profile Duct occluder device for neonates and infants compatible with 4F delivery system\" |
| 731 | (EX) Single disc duct occluders with with sizes from 3mm onwards up to 20 mm ..Should be FDA\" or CE\" andDCGI approved ( DEVICE alone) |
| 732 | (D) (EX) Delivery cable for Single disk duct occluders (the cablewill be procured from the same company who is selected as L1 in the category\"Single disc duct occluders with sizes from 3mm onwards up to 20 mm ..Should be FDA\" or CE\" and DCGI approved\" |
| 733 | VSD DEVICES |
| 734 | (EX)Ventricular septal defect Closure Devices All sizes ( 4mm to18 mm).Should be FDA\"/CE\"/DCGI approved ( DEVICE only) |
| 735 | (EX) Delivery cable Ventricular septal defect closure (the cablewill be procured from the same company who is selected as L1 in the category- \" Ventricular septal defect Closure Devices All sizes ( 4mm to18 mm).Should be FDA\"/CE\"/DCGI approved\" |
| 736 | (EX)Muscular VSD Closure Devices-All sizes with delivery cable - cost of cable and device should be mentioned separately.Should be FDA\"/CE\"/DCGI approved |
| 737 | (EX) Low profile Delivery sheathfor VSD closure devices( 5F to 14F).Should be CE\" and DCGI approved |
| 738 | (EX)Ventricular septal defect Closure Devices All sizes with delivery system and delivery cable.Should be FDA\"/CE\" and DCGI approved |
| 739 | (EX)Ventricular septal defect Closure Devices ( ONLY Device) All sizes .Should be FDA\" /CE\" and DCGI approved |
| 740 | (EX)Delivery cable for the item \"Ventricular septal defect Closure Devices ( ONLY Device) All sizes.Should be FDA\" /CE\" and DCGI approved (the cable will be procured from the same company who is selected as L1 in the item mentioned above |
| 741 | (EX) Post Infarct ventricular septal rupture Closure Devices- All sizes and types.FDA approved |
| 742 | (EX) Ventricular septal defect (device alone) for antegrade closure .Should be FDA\" or CE\" and DCGI approved |
| 743 | (EX) Extra soft Nitinol multi-functional Closure Devices ( ONLY DEVICE) compatible with guide catheter and delivery cables attachable to both ends of the device.deliverable with a minimum of atleast 4Fr delivery system .Should be CE/DCGI approved |
| 744 | (S) 4 F AND 5 F catheter COMPATABLE PERI MEMBRANEUOUS VSD DEVICE with double screw design for antegrade and retrograde closure ( DEVICE ONLY).Should beCE\" AND DCGI approved |
| 745 | (S)(EX)Braided kink resistant long(100-120cm) delivery sheaths for VSD closure all sizes.Should be FDA\"/CE\"/DCGI approved |
| 746 | (S)(EX)COOK LONG SHEATHS CAPABLE OF ASD/VSD/PDA device delivery SIZES 6Fto 16F.Should be FDA\"/CE\"/DCGI approved |
| 747 | LA APPENDAGE EXCLUSION |
| 748 | (D)(EX)Left atrial appendage closure device with delivery system all sizes.Should be FDA\"/CE\"/DCGI approved |
| 749 | TRANSCATHETER VALVE REPLACEMENT & REPAIR |
| 750 | (EX)Trans catheter aortic valve (self-expanding) with delivery systems and all accessories .Should be FDA\"/CE\"/DCGI approved |
| 751 | (EX)Trans catheter aortic valve (balloon expanding)with delivery systems and all accessories.Should be FDA\"/CE\"/DCGI approved |
| 752 | (EX)Trans catheter aortic valve delivery sheath( for self expanding).Should be FDA\"/CE\"/DCGI approved |
| 753 | (EX)Trans catheter aortic valve delivery sheath(balloon expanding).Should be FDA\"/CE\"/DCGI approved |
| 754 | (EX)Transcatheter mitral valve repair system with accessories.Should be FDA\"/CE\"/DCGI approved |
| 755 | (EX)Transcatheter tricuspid valve repair system with accessories.Should be FDA\"/CE\"/DCGI approved |
| 756 | (EX)Percutaneous bicaval self expanding valve system for severe tricuspid regurgitation with accessories. Should be FDA\"/CE\"/DCGI approved |
| 757 | (EX)Transcatheter balloon expandable pulmonary valve with delivery system. Should be FDA/CE/DGCI approved |
| 758 | (EX)Transcatheter self expanding pulmonary valve with delivery system. Should be FDA/CE/DGCI approved |
| 759 | (EX)Large bore long femoral sheaths 12-18 F for aortic/TAVI interventions.Should be FDA\"/CE\"/DCGI approved |
| 760 | TEVAR/EVAR |
| 761 | (EX)Large diameter (14-20mm) balloon expanding aortic/ vena caval stents.Should be FDA\"/CE\"/DCGI approved |
| 762 | (EX)Coda balloon for optimalAortic Stent expansion .Should be FDA\" or CE\" and DCGI approved |
| 763 | (EX)Anzel sheaths for fenestarted EVAR .Should be FDA\"/CE\"/DCGI approved |
| 764 | (EX)Balloon expandable covered stents(sizes 5-20mm) for fenestrated TEVAR/EVAR.Should be FDA\"/CE\"/DCGI approved |
| 765 | (EX)Expandable femoral sheaths for balloon expandable valves .Should be FDA\"/CE\"/DCGI approved |
| 766 | (EX)Braided kink resistant flexible sheaths (60-100cm) for fenestarted TEVAR and carotid interventions-straight and curved.Should be FDA\"/CE\"/DCGI approved |
| 767 | (EX)LARGE DIAMETERCOVERED AORTA-ARCH AND ZONE 2STENT GRAFTS TAA all sizes.Should be FDA\"/CE\"/DCGI approved |
| 768 | (EX) Aorto Uni iliac stent coveredgrafts All sizes.Should beCE\" AND DCGI approved |
| 769 | (EX)AORTIC STENT covered GRAFTSfor DTA aneurysm stenting .Should be FDA\"/CE\"/DCGI approved |
| 770 | (EX) Low profile Dacron / PTFE covered stent grafts ( 20-45mm) for sealing extensive aortic dissection .Should beCE\" AND DCGI approved |
| 771 | (EX) Low profile hydrophilic sheaths for aortic procedures ( 12 F and above) .Should be FDA\"/CE\"/DCGI approved |
| 772 | (EX) Covered stent grafts for aortic arch aneurysm withonsite fenestraion capability.Should be FDA\"/CE\"/DCGI approved |
| 773 | (EX) Aortic covered Stent grafts (straight) capable for fenestration for justa renal and juxta subclavain aneurysms and traumatic aortic injury.Should be FDA\"/CE\"/DCGI approved |
| 774 | (EX) ABDOMINAL AORTIC ANEURYSM STENT GRAFTS WITH ILIAC LIMBS for abd aorta aneurysm.Should be FDA\"/CE\"/DCGI approved |
| 775 | SPECIAL CATHETERS & IMPLANTS |
| 776 | Impella catheter for percutaneous cardiopulmonary support 2.5 LPM |
| 777 | Impella catheter for percutaneous cardiopulmonary support 5 LPM |
| 778 | (EX)Large bore low profile manual aspiration system for high thrombus load from peripheral arteries/veins .Should be FDA\"/CE\"/DCGI approved |
| 779 | (S)Bioptomes for Endomyocardial biopsy :Bioptomes ; 5.2F .Should be FDA\"/CE\"/DCGI approved |
| 780 | (EX)BIOPTOME for Endomyocardial biopsy 6F.Should be FDA\"/CE\"/DCGI approved |
| 781 | (S)Swan Ganz capable of accommodating 0.038\" Guide Wire Large Lumen Size7F .Should be FDA\"/CE\"/DCGI approved |
| 782 | (S)Swan Ganz capable of accommodating 0.032/035\" Guide Wire Large Lumen Size6F .Should be FDA\"/CE\"/DCGI approved |
| 783 | (S Balloon atrial septostomy catheter.Should be FDA\"/CE\"/DCGI approved |
| 784 | (D)VENA CAVA FILTER- Retrivable, Jugular Deployement.Should be FDA\"/CE\"/DCGI approved |
| 785 | (D)VENA CAVA FILTER- Retrivable, Femoral Deployement.Should be FDA\"/CE\"/DCGI approved |
| 786 | (D)VENA CAVA FILTER- RETRIVAL SYSTEM .Should be FDA\"/CE\"/DCGI approved |
| 787 | Intracardiac echocardiography catheter is compatible with ILAB Echo system. |
| 788 | Intracardiac echocardiography catheter compatible with Philips Echo system. |
| 789 | TRANS SEPTAL PUNCTURE |
| 790 | SSIR - Single chamber rate responsive implantable multiprogrammable pacemakerwith maximum programmable sensitivity of 0.5 mv or more with matching leads and subclavian introducer set to be quoted as one set. Active fixation leads should be supplied as atrial (50%) / ventricular (50%).Should be FDA\"/CE\"/DCGI approved |
| 791 | VDD implantable multiprogrammable pacemaker with shortest programmable AV delay of 50 ms, with matching single pass steroid eluting VDD lead and matching sublavian introducer. .Should be FDA\"/CE\"/DCGI approved |
| 792 | DDD - Dual chamber implantable multiprogrammable pacemaker with shortest programmable Av delay of 50 ms, with matching set of steroid eluting active fixation atrial and ventricular leads and two matching subclavian introducers..Should be FDA\"/CE\"/DCGI approved |
| 793 | DDDR - Dual chamber rate-responsive implantable multiprogrammable pacemaker withshortest programmable Av delay of 50 ms, with matching set of steroid eluting active fixation atrial and ventricular leads and two matching subclavian introducers..Should be FDA\"/CE\"/DCGI approved |
| 794 | Bipolar lead specially designed for placement in coronary sinus for LV pacing. Should besupplied with 9F short sheath with valve, long preshaped slittable sheaths in various shapes for CS cannulation and inner subselective sheath. Lead, long sheath, subselective sheath and short sheath should be quoted as one set..Should be FDA\"/CE\"/DCGI approved |
| 795 | CATH LAB INJECTABLES |
| 796 | (S)Contrast Media for Angiography and Angioplasty (Non-Ionic 350 mg I/ml,100 ml Bottles).Should be FDA\"/CE\"/DCGI approved |
| 797 | (S)Contrast Media for Angiography and Angioplasty (Non-Ionic 350 mg I/ml, 50 ml Bottles).Should be FDA\"/CE\"/DCGI approved |
| 798 | (S)Iso Osmolar Contrast Media for Angiography and Angioplasty for Patients with Renal Dysfunction (Non-Ionic 320 mg I/ml, 100 ml Bottles).Should be FDA\"/CE\"/DCGI approved |
| 799 | (S)Iso Osmolar Contrast Media for Angiography and Angioplasty for Patients with Renal Dysfunction (Non-Ionic 320 mg I/ml 50 ml Bottles).Should be FDA\"/CE\"/DCGI approved |
| 800 | (S)Myocardial Echocardiographic Contrast comprising of Sulphur Hexachloride or equivalent Micro Bubbles.Should be FDA\"/CE\"/DCGI approved |
| 801 | Inj TIROFIBAN 100 mL bottles.Should be FDA\"/CE\"/DCGI approved |
| 802 | Injection sildenafil 10 mg vial.Should be FDA\"/CE\"/DCGI approved |
| 803 | Injection Nicorandil 48 mg vial.Should be FDA\"/CE\"/DCGI approved |
| 804 | Injection Nicorandil 2 mg vial.Should be FDA\"/CE\"/DCGI approved |
| 805 | Injection milrenone 10 mg vial. Should be FDA\"/CE\"/DCGI approved |
| 806 | Injection Cangrelor 50 mg vial. Should be FDA\"/CE\"/DCGI approved |
| 807 | Injection BIVALURIDIN 250 mg vial .Should be FDA\"/CE\"/DCGI approved |
| 808 | Injection TENECTAPLASE 30mg Should be FDA\"/CE\"/DCGI approved |
| 809 | Injection TENECTAPLASE 40mg Should be FDA\"/CE\"/DCGI approved |
| 810 | Injection TENECTAPLASE 50mg Should be FDA\"/CE\"/DCGI approved |
| 811 | BIOMARKERS |
| 812 | (D)TROPONIN IQUANTITATIVE BED SIDE TEST KIT .Should be FDA\"/CE\"/DCGI approved Measuring Device to be supplied |
| 813 | (D)TROPONIN TQUANTITATIVE BED SIDE TEST KIT.Should be FDA\"/CE\"/DCGI approved Measuring Device to be supplied |
| 814 | (D)HIGH SENSITIVE TROPONIN T QUANTITIVE QUANTITATIVE BED SIDE TEST KIT.Should be FDA\"/CE\"/DCGI approved Measuring Device to be supplied |
| 815 | (D)HIGH SENSITIVE TROPONIN I QUANTITATIVE- FDA approved-Analyser Should be Supplied.Should be FDA\" approved Measuring Device to be supplied |
| 816 | (D)N-TERMINAL PRO BNP QUANTITATIVE BED SIDE TEST KIT.Should be FDA\"/CE\"/DCGI approved Measuring Device to be supplied |
| 817 | (D)N-TERMINALBNPQUANTITATIVE BED SIDE TEST KIT.Should be FDA\"/CE\"/DCGI approved Measuring Device to be supplied |
| 818 | (D)D-TIMER QUANTITATIVE BED SIDE TEST KIT.Should be FDA\"/CE\"/DCGI approved Measuring Device to be supplied |
| 819 | (D)Bedside Lipid Profile Measurement Kits.Reading Machine should be provided |
| 820 | (D)Bedside INR Measurement Kits.Reading Machine should be provided |
| 821 | (D) ACT cartridges.Reading Machine should be provided |
| 822 | RADIATION PROTECTION |
| 823 | (D)Vinyl layered LEAD FREE aprons superior quality imported types for radiation protection during interventional procedures. COVERING BOTH FRONT AND BACKSINGLE PIECE MEDIUM SIZE.Should be FDA\"/CE\"/DCGI approved & Item to be Demonstrated to departmental selection committee |
| 824 | (D)Vinyl layered LEAD FREE aprons superior quality imported types for radiation protection during interventional procedures. COVERING BOTH FRONT AND BACKSINGLE PIECE LARGE SIZE.Should be FDA\"/CE\"/DCGI approved & Item to be Demonstrated to the departmental selection committee |
| 825 | (D)Vinyl layered LEAD FREE aprons superior quality imported types for radiation protection during interventional procedures. COVERING BOTH FRONT AND BACKTWOPIECE SKIRT AND BLOUSE TYPE MEDIUM SIZE. .Should be FDA\"/CE\"/DCGI approved & Item to be Demonstrated to departmental selection committee |
| 826 | (D)Vinyl layered LEAD FREE aprons superior quality imported types for radiation protection during interventional procedures. COVERING BOTH FRONT AND BACKTWOPIECE SKIRT AND BLOUSE TYPE LARGE SIZE.Should be FDA\"/CE\"/DCGI approved & Item to be Demonstrated to departmental selection committee |
| 827 | (D)Vinyl layered LEAD FREE aprons superior quality imported types for radiation protection during interventional procedures. COVERING FRONT only SINGLE PIECE SMALL SIZE.Should be FDA\"/CE\"/DCGI approved & Item to be Demonstrated to departmental selection committee |
| 828 | (D)Vinyl layered LEAD FREE aprons superior quality imported types for radiation protection during interventional procedures. COVERING FRONT only SINGLE PIECE MEDIUM SIZE.Should be FDA\"/CE\"/DCGI approved & Item to be Demonstrated to departmental selection committee |
| 829 | (D)Vinyl layered LEAD FREE aprons superior quality imported types for radiation protection during interventional procedures. COVERING FRONT only SINGLE PIECE LARGE SIZE.Should be FDA\"/CE\"/DCGI approved & Item to be Demonstrated to departmental selection committee |
| 830 | (D)Sterile lead-free disposable radiation protection shield.Should be FDA\"/CE\"/DCGI approved |
| 831 | (D)Soft flexible Thyroid Collars Radiation Protection.Should be FDA\"/CE\"/DCGI approved & Item to be Demonstrated to departmental selection committee |
| 832 | (D)Gonadal Shields Radiation Protection.Should be FDA\"/CE\"/DCGI approved & Item to be Demonstrated to departmental selection committee |
| 833 | (D)Radaiation Protective Eye Goggles.Should be FDA\"/CE\"/DCGI approved & Item to be Demonstrated to departmental selection committee |
| 834 | (D)Radaiation Protective Head Gear.Should be FDA\"/CE\"/DCGI approved & Item to be Demonstrated to departmental selection committee |
| 835 | (D)Radiation protection drape pads.Should be FDA\"/CE\"/DCGI approved |
| 836 | ELECTROPHYSIOLOGY |
| 837 | 5 French fixed curve quadripolar catheter with 2-5-2 interelectrode spacing. One matching connector for every 5 catheters.Should be FDA\"/CE\"/DCGI approved |
| 838 | 6 French deflectable quadripolar catheter with 2-5-2 interelectrode spacing and matching connector.Should be FDA\"/CE\"/DCGI approved |
| 839 | 6 French deflectable decapolar catheter with 2-5-2 interelectrode spacing and matching connector.Should be FDA\"/CE\"/DCGI approved |
| 840 | 4 or 5 French fixed curve decapolar catheter with 2-5-2 interelectrode for coronary sinus placement. Should be FDA\"/CE\"/DCGI approved |
| 841 | 7 French deflectable duodecapolar catheters with 2-5-2 interelectrode spacing with matching connectors.Should be FDA\"/CE\"/DCGI approved |
| 842 | 7 French deflectable duodecapolar catheters with 2-8-2-(60)-2-8-2 interelectrode spacing with matching connectors.Should be FDA\"/CE\"/DCGI approved |
| 843 | 6 French fixed curve 20-pole catheter with 2-2-2 spacing for mapping in Crista region |
| 844 | 20-pole variable diameter circular mapping catheter for mapping in pulmonary veins |
| 845 | 7 French quadripolar Radiofrequency ablation catheter with a 4 mm tip, unidirectional deflection, availability in small, medium and large curves. Should be compatible with Stockert and IBI RF generators and Suitable connecting cable should be provided for every 5 catheters..Should be FDA\"/CE\"/DCGI approved |
| 846 | 7 French quadripolar Radiofrequency ablation catheter with a 4 mm tip, bidirectional deflection, availability in small, medium and large curves. Should be compatible with Stockert and IBI RF generators and suitable connecting cables should be provided .Should be FDA\"/CE\"/DCGI approved |
| 847 | 7 French quadripolar Radiofrequency ablation catheter with a 8 mm tip, unidirectional deflection, availability in medium and large curves. Should be compatible with Stockert and IBI RF generators and Suitable connecting cable should be provided for every 5 catheters..Should be FDA\"/CE\"/DCGI approved |
| 848 | 7 French quadripolar Radiofrequency ablation catheter with a 8 mm tip, bidirectional deflection, availability in medium and large curves. Should be compatible with Stockert and IBI RF generators and Suitable connecting cable should be provided for every 5 catheters..Should be FDA\"/CE\"/DCGI approved |
| 849 | 7 French quadripolar Radiofrequency ablation catheter with irrigated tip, unidirectional deflection and availability in medium and large curves. Should be compatible with Stockert and IBI RF generators and Suitable connecting cable should be provided for every 5 catheters. Tubing set for irrigation to be provided with each catheter.Should be FDA\"/CE\"/DCGI approved |
| 850 | 7 French quadripolar Radiofrequency ablation catheter with irrigated tip, bidirectional deflection and availability in medium and large curves. Should be compatible with Stockert and IBI RF generators and Suitable connecting cable should be provided for every 5 catheters. Tubing set for irrigation to be provided with each catheter. Should be FDA\"/CE\"/DCGI approved |
| 851 | Quadripolar, irrigated tip, Radiofrequency ablation catheter with a 3.5 mm tip and unidirectional deflection for use with the CARTO mapping system. Should include irrigation tubing set for interface between the irrigation pump and the ablation catheter and matching external reference patch for use with the CARTO 3 system.Should be FDA\"/CE\"/DCGI approved |
| 852 | Quadripolar, irrigated tip, Radiofrequency ablation catheter with a 3.5 mm tip and bidirectional deflection for use with the CARTO mapping system. Should include irrigation tubing set for interface between the irrigation pump and the ablation catheter and matching external reference patch for use with the CARTO 3 system.Should be FDA\"/CE\"/DCGI approved |
| 853 | Quadripolar, irrigated tip, Radiofrequency ablation catheter with a 3.5 mm tip, bidirectional deflection and contact force sensing for use with the CARTO mapping system. Should include irrigation tubing set for interface between the irrigation pump and the ablation catheter and matching external reference patch for use with the CARTO 3 system.Should be FDA\"/CE\"/DCGI approved |
| 854 | Multipolar mapping catheter for use with the CARTO mapping system (Pentaray Nav) |
| 855 | Surface electrode kit for use with the Ensite NavX system including 3 pairs of surface patches, 10 ECG electrodes and 1 system reference electrode .Should be FDA\"/CE\"/DCGI approved |
| 856 | Multipolar mapping catheter suitable for omnipolar mapping with the Ensite NavX system |
| 857 | Reusable indifferent electrode pad compatible with the Stockert ablator.Should be FDA\"/CE\"/DCGI approved |
| 858 | Balloon catheter for cryoablation of pulmonary veins with all required accessories including mapping catheter and steerable sheath |
| 859 | Long deflectable sheath with hemostatic valve, side port, atraumatic tip, braided shaft, uni- or bidirectional steerability, availability in small, medium or large curves, minimum inner diameter or 7F, minimum length of 65 cms.Should be FDA\"/CE\"/DCGI approved |
| 860 | Steerable, long sheath introducer of at least 8F inner diameter, with atraumatic tip and bidirectional steering, designed for use in epicardial mapping.Should be FDA\"/CE\"/DCGI approved |
| 861 | IMPLANTS Single Chamber |
| 862 | SSIR - Single chamber rate responsive implantable multiprogrammable pacemaker with maximum programmable sensitivity of 0.5 mv or more with matching leads and subclavian introducer set to be quoted as one set. Active fixation leads should be supplied as atrial (50%) / ventricular (50%). Should be FDA\"/CE\"/DCGI approved |
| 863 | MRI SSIR - Single chamber rate responsible implantable multiprogrammable MRI conditional pacemaker with matching MRI conditional atrial or ventricular active fixation lead and introducer sheath set. .Should be FDA\"/CE\"/DCGI approved |
| 864 | IMPLANT DUAL CHAMBER |
| 865 | DDD - Dual chamber implantable multiprogrammable pacemaker with shortest programmable AV delay of 50 ms, with matching set of steroid eluting active fixation atrial and ventricular leads and two matching subclavian introducers. Should be FDA\"/CE\"/DCGI approved |
| 866 | DDDR - Dual chamber rate-responsive implantable multiprogrammable pacemaker withshortest programmable AV delay of 50 ms, with matching set of steroid eluting active fixation atrial and ventricular leads and two matching subclavian introducers. Should be FDA\"/CE\"/DCGI approved |
| 867 | MRI DDDR - Dual chamber MRI conditional pacemaker with matching MRI conditional atrial and ventricular active fixation leads and 2 introducer sheath sets. Should be FDA\"/CE\"/DCGI approved |
| 868 | AICD |
| 869 | Single chamber, Single Coil DF4 AICD - Single chamber, implantable cardioverter defibrillator for treatment of life threatening ventricular arrhythmias with facility for bradycardia pacing and tiered therapy for tachycardias, maximum shock energy of at least 35 J, with matching single coil, integrated bipolar active fixation ventricular leads. Should be FDA\"/CE\"/DCGI approved |
| 870 | Single chamber, Dual coil DF4 AICD - Single chamber, implantable cardioverter defibrillator for treatment of life threatening ventricular arrhythmias with facility for bradycardia pacing and tiered therapy for tachycardias, maximum shock energy of at least 35 J, with matching dual coil, integrated bipolar active fixation ventricular leads..Should be FDA\"/CE\"/DCGI approved |
| 871 | Single chamber, Single Coil MRI conditional DF4 AICD - Single chamber, MRI conditional implantable cardioverter defibrillator for treatment of life threatening ventricular arrhythmias with facility for bradycardia pacing and tiered therapy for tachycardias, maximum shock energy of at least 35 J, with matching single coil, integrated bipolar active fixation MRI conditional ventricular leads. Should be FDA\"/CE\"/DCGI approved |
| 872 | Dual chamber Single coil DF4 AICD - Dual chamber, implantable cardioverter defibrillator for treatment of life threatening ventricular arrhythmias with facility for bradycardia pacing and tiered therapy for tachycardias, maximum shock energy of atleast 35 J, with matching single coil, integrated bipolar active fixation atrial and ventricular leads..Should be FDA\"/CE\"/DCGI approved |
| 873 | Dual chamber Dual Coil DF4 AICD - Dual chamber, implantable cardioverter defibrillator for treatment of life threatening ventricular arrhythmias with facility for bradycardia pacing and tiered therapy for tachycardias, maximum shock energy of atleast 35 J, with matching dual coil, integrated bipolar active fixation atrial and ventricular leads..Should be FDA\"/CE\"/DCGI approved |
| 874 | Dual chamber Single coil MRI conditional DF4 AICD - Dual chamber, MRI conditional implantable cardioverter defibrillator for treatment of life threatening ventricular arrhythmias with facility for bradycardia pacing and tiered therapy for tachycardias, maximum shock energy of atleast 35 J, with matching single coil, integrated bipolar active fixation MRI conditional atrial and ventricular leads..Should be FDA\"/CE\"/DCGI approved |
| 875 | Single chamber subcutaneous ICD with lead designed for subcutaneous placement, introducer and other accessories |
| 876 | CRT-P & D |
| 877 | CRT-P-Triple chamber pacing system comprising pacemaker, active fixation atrial, active fixation RV leads and passive bipolar over the wire coronary sinus lead (LV lead). Should include compatible short sheaths with valve, long preshaped slittable sheaths for coronary sinus cannulation in multiple shapes, subselective inner sheaths, guidewire and occlusion balloon catheter for coronary venography. Coronary sinus lead should be available in multiple curves \"/ sizes..Should be FDA\"/CE\"/DCGI approved |
| 878 | CRT-P-Triple chamber pacing system comprising pacemaker, active fixation atrial, active fixation RV leads and passive quadripolar over the wire coronary sinus lead (LV lead). Should include compatible short sheaths with valve, long preshaped slittable sheaths for coronary sinus cannulation in multiple shapes, subselective inner sheaths, guidewire and occlusion balloon catheter for coronary venography. Coronary sinus lead should be available in multiple curves \"/ sizes..Should be FDA\"/CE\"/DCGI approved |
| 879 | CRT-P-Triple chamber pacing system comprising pacemaker, active fixation atrial, active fixation RV leads and active fixation Quadripolar over the wire coronary sinus lead (LV lead) specifically with built in screw in type of mechanism for maintaining stable position. Should include compatible short sheaths with valve, long preshaped slittable sheaths for coronary sinus cannulation in multiple shapes, subselective inner sheaths, guidewire and occlusion balloon catheter for coronary venography. Coronary sinus lead should be available in multiple curves \"/ sizes..Should be FDA\"/CE\"/DCGI approved |
| 880 | MRI CRT-P-Triple chamber pacing system comprising MRI conditional pacemaker, active fixation MRI conditional atrial, active fixation MRI conditional RV leads and passive quadripolar over the wire MRI conditional coronary sinus lead (LV lead). Should include compatible short sheaths with valve, long preshaped slittable sheaths for coronary sinus cannulation in multiple shapes, subselective inner sheaths, guidewire and occlusion balloon catheter for coronary venography. Coronary sinus lead should be available in multiple curves \"/ sizes..Should be FDA\"/CE\"/DCGI approved |
| 881 | MRI CRT-P-Triple chamber pacing system comprising MRI conditional pacemaker, MRI conditional active fixation atrial, MRI conditional active fixation RV leads and MRI conditional active fixation Quadripolar over the wire coronary sinus lead (LV lead) specifically with built in screw in type of mechanism for maintaining stable position. Should include compatible short sheaths with valve, long preshaped slittable sheaths for coronary sinus cannulation in multiple shapes, subselective inner sheaths, guidewire and occlusion balloon catheter for coronary venography. Coronary sinus lead should be available in multiple curves \"/ sizes..Should be FDA\"/CE\"/DCGI approved |
| 882 | Single coil DF-4 CRT-D - Triple Chamber Pacemaker System with cardioverter defibrillator for treatment of life threatening ventricular arrhythmias with facility for CRT pacing and tiered therapy for tachycardias, maximum shock energy of atleast 35 J comprising active fixation atrial lead, single coil with integrated bipolar active fixation RV lead and passive Quadripolar over the wire coronary sinus lead (LV lead). Should include compatible short sheaths with valve, long preshaped slittable sheaths for coronary sinus cannulation in multiple shapes, subselective inner sheaths, guidewire and occlusion balloon catheter for coronary venography. Coronary sinus lead should be available in multiple curves \"/ sizes.Should be FDA\"/CE\"/DCGI approved |
| 883 | Single coil DF-4 CRT-D - Triple Chamber Pacemaker System with cardioverter defibrillator for treatment of life threatening ventricular arrhythmias with facility for CRT pacing and tiered therapy for tachycardias, maximum shock energy of atleast 35 J comprising active fixation atrial lead, single coil with integrated bipolar active fixation ventricular RV lead and active fixation Quadripolar over the wire coronary sinus lead (LV lead) specifically with built in screw in type of mechanism for maintaining stable position.Should include compatible short sheaths with valve, long preshaped slittable sheaths for coronary sinus cannulation in multiple shapes, subselective inner sheaths, guidewire and occlusion balloon catheter for coronary venography. Coronary sinus lead should be available in multiple curves \"/ sizes.Should be FDA\"/CE\"/DCGI approved |
| 884 | MRI conditional Single coil DF-4 CRT-D - Triple Chamber MRI conditional Pacemaker System with cardioverter defibrillator for treatment of life threatening ventricular arrhythmias with facility for CRT pacing and tiered therapy for tachycardias, maximum shock energy of atleast 35 J comprising active fixation MRI conditional atrial lead, single coil with integrated bipolar active fixation MRI conditional RV lead and passive Quadripolar over the wire MRI conditional coronary sinus lead (LV lead). Should include compatible short sheaths with valve, long preshaped slittable sheaths for coronary sinus cannulation in multiple shapes, subselective inner sheaths, guidewire and occlusion balloon catheter for coronary venography. Coronary sinus lead should be available in multiple curves \"/ sizes.Should be FDA\"/CE\"/DCGI approved |
| 885 | MRI conditional Single coil DF-4 CRT-D - Triple Chamber Pacemaker System with cardioverter defibrillator for treatment of life threatening ventricular arrhythmias with facility for CRT pacing and tiered therapy for tachycardias, maximum shock energy of atleast 35 J comprising active fixation MRI conditional atrial lead, single coil with integrated bipolar active fixation MRI conditional RV lead and active fixation Quadripolar over the wire MRI conditional coronary sinus lead (LV lead) specifically with built in screw in type of mechanism for maintaining stable position.Should include compatible short sheaths with valve, long preshaped slittable sheaths for coronary sinus cannulation in multiple shapes, subselective inner sheaths, guidewire and occlusion balloon catheter for coronary venography. Coronary sinus lead should be available in multiple curves \"/ sizes.Should be FDA\"/CE\"/DCGI approved |
| 886 | CONDUCTION SYSTEM PACING |
| 887 | Single chamber SSIR for Conduction system pacing-Single chamber rate responsive implantable multiprogrammable pacemaker with lead and specialised long sheath designed for conduction system pacing, compatible short sheaths with valve and other accessories required for conduction system pacing. Should be FDA\"/CE\"/DCGI approved. |
| 888 | MRI conditional Single chamber SSIR for Conduction system pacing-Single chamber rate responsive implantable multiprogrammable pacemaker with lead and specialised long sheath designed for conduction system pacing, compatible short sheaths with valve and other accessories required for conduction system pacing. Should be FDA\"/CE\"/DCGI approved. |
| 889 | MRI conditional Dual chamber DDDR for Conduction system pacing-Dual chamber rate-responsive implantable multiprogrammable MRI conditional pacemakerwith active fixation MRI conditional atrial lead, lead with specialised long sheath designed for conduction system pacing, compatible short sheaths with valve and other accessories for conduction system pacing. Should be FDA\"/CE\"/DCGI approved |
| 890 | Conduction system pacing optimised CRT-P-Triple chamber pacing system comprising pacemaker, active fixation atrial lead, quadripolar coronary sinus lead, lead with specialised long sheath designed for condution system pacing. Should include long preshaped slittable sheaths for coronary sinus cannulation in multiple shapes, subselective inner sheaths, guidewire, occlusion balloon catheter for coronary venography, compatible short sheaths with valve and sheath slitters. Coronary sinus lead should be available in multiple curves \"/ sizes. Should be FDA\"/CE\"/DCGI approved |
| 891 | MRI conditional Conduction system pacing optimised CRT-P-Triple chamber pacing system comprising MRI conditional pacemaker, active fixation MRI conditional atrial lead, quadripolar MRI conditonal coronary sinus lead, lead with specialised long sheath designed for condution system pacing. Should include long preshaped slittable sheaths for coronary sinus cannulation in multiple shapes, subselective inner sheaths, guidewire, occlusion balloon catheter for coronary venography, compatible short sheaths with valve and sheath slitters. Coronary sinus lead should be available in multiple curves \"/ sizes. Should be FDA\"/CE\"/DCGI approved |
| 892 | MRI conditional Conduction system pacing optimised CRT-P-Triple chamber pacing system comprising MRI conditional pacemaker, active fixation MRI conditional atrial lead, active fixation & screw in type of quadripolar MRI conditional coronary sinus lead (LV lead), MRI conditional lead with specialised long sheath designed for condution system pacing. Should include long preshaped slittable sheaths for coronary sinus cannulation in multiple shapes, subselective inner sheaths, guidewire, occlusion balloon catheter for coronary venography, compatible short sheaths with valve and sheath slitters. Coronary sinus lead should be available in multiple curves \"/ sizes. Should be FDA\"/CE\"/DCGI approved |
| 893 | PACING LEADS |
| 894 | Steroid eluting bipolar active fixation atrial leads with introducer sheath.Should be FDA\"/CE\"/DCGI approved |
| 895 | Steroid eluting bipolar active fixation ventricular leads with introducer sheath.Should be FDA\"/CE\"/DCGI approved |
| 896 | Single and Dual coil (50-50%), integrated bipolar active fixation DF4 type ICD leads.Should be FDA\"/CE\"/DCGI approved |
| 897 | Quadripolar lead specially designed for placement in coronary sinus for LV pacing. Should be supplied with 9F short sheath with valve, long preshaped slittable sheaths in variousshapes for CS cannulation and inner subselective sheath. Lead, long sheath, subselective sheath and short sheath should be quoted as one set. Should be FDA\"/CE\"/DCGI approved |
| 898 | Quadripolar lead specially designed for placement in coronary sinus for LV pacing with built in screw in type of active fixation mechanism for maintaining stable position. Should be supplied with compatible short sheath with valve, long preshaped slittable sheaths in various shapes for CS cannulation and inner subselective sheath. Lead, long sheath, subselective sheath and short sheath should be quoted as one set. Should be FDA\"/CE\"/DCGI approved |
| 899 | Lumenless Lead with preshaped sheath (specifically designed for conduction system pacing) along with slitter and short subclavian sheath as one set. |
| 900 | Stylet driven ventricular lead for conduction system pacing with sheath and other compatible accessories. |
| 901 | Unipolar epicardial pacing leads |
| 902 | Bipolar epicardial pacing leads |
| 903 | LEADLESS PACEMAKER |
| 904 | Miniaturised pacemaker for use as leadless pacemaker with delivery system and other required accessories |
| 905 | TEMPORARY PACING |
| 906 | (S)Temporary Pacing Leads sizes with 5F/6F.Should be FDA\"/CE\"/DCGI approved |
| 907 | (S)Balloon Flow Assisted Temporary Pacing lead(5F and 6F .Should be FDA\"/CE\"/DCGI approved |
| 908 | (D)Single Chamber Demand Cum Overdrive Temporary Pulse Generators with various Dual Chamber and Single Chamber modes, capable of overdrive pacing.Should be FDA\"/CE\"/DCGI approved |
| 909 | (D)Dual Chamber Demand Cum Overdrive Temporary Pulse Generators withvarious Dual Chamber and Single Chamber modes, capable of overdrive pacing.Should be FDA\"/CE\"/DCGI approved |
| 910 | LOOP RECORDERS/REMOTE MONITORING |
| 911 | (D)IMPLANTABLE loop recorder - long term ( ILR) for subcutaneous implantation, capable of recording at least one channel subcutaneous ECG. Matching hand-held activator should be provided. .Should be FDA\"/CE\"/DCGI approved |
| 912 | (D) EXTERNAL DISPOSABLEexternal loop recorder with capability to record at least one ECG lead for a period of at least 7 days. Recording patch / electrodes should be water resistant allowing patient to bathe. Episodes should be identified automatically and it should also be possible to record patient triggered episodes. Transmission should be wireless and monitored in a 24x7 staffed monitoring center. Quoted cost should include disposable electrode set, recorder, hand-held activator, data transmission and reporting for the period of recording..Should be FDA\"/CE\"/DCGI approved |
| 913 | (D) Wrist Wearable, reusable recorder capable of remote monitoring of physical activity by step count and physical inactivity, heart rate, SpO2, and sleep, with rechargeable battery lasting at least 72 hours between charges compatible with android OS. Waterproof with a year warranty. |
| 914 | (D) Wrist Wearable, reusable recorder capable of remote monitoring of physical activity by step count and physical inactivity, heart rate, SpO2, and sleep, with rechargeable battery lasting at least 72 hours between charges compatible with iOS . Waterproof with a year warranty. |
| 915 | (D) Wrist Wearable, reusable rechargable recorder capable of remote monitoring of physical activity by step count and physical inactivity, heart rate, SpO2, and sleep, with rechargeable battery lasting at least 72 hours between charges compatible with both Android and iOS . Waterproof with a year warranty. |
| 916 | (D) Medical grade reusable rechargeable monitoring wrist wearable device for remote monitoring of continuous pulse rate, physical activity, respiration rate and patient triggered ECG and SpO2. Automated arrhythmia warning on PPG and automated Arrhythmia diagnosis on ECG. Remote recording of PPG and ECG waveforms should be possible. Battery life should be a minimum 48 hours and waterproof atIP67 or above. Patient data should be visible to the patient via an Android or iOS smartphone and to the physician via a web interphase. The unit should be CDSCO certified and US FDA approved for PPG-based arrhythmia and ECG arrhythmia diagnosis and if not human clinical trial data indicating a specificty and sensitivity of 95% or above should be submitted. The unit should have 3-year warranty. |
| 917 | SURGICAL INSTRUMENTS |
| 918 | (D)One set of high grade stainless steel surgical instruments for minor surgical procedure. Must include the following instruments – Sponge forceps 2 Nos, Towel clamp – 4, Hemostatic Crile forceps straight – 4, hemostatic Crile forceps curved – 6, Allis tissue forceps – 2, Mayo Hegar needle holder 6 inches – 1, Mayo Hegar needle holder 7 inches – 1, Mayo scissors straight – 1, Metzenbaum scissors curved – 1, Small curved scissors – 1, small straight scissors – 1, thumb forceps – 2, adsons toothed forceps – 2, Knife handle #7 – 1, knife handle #4 – 1, Weitlaner self retaining retractor sharp 5 inches – 1, double hook retractor – 2, right angle forceps – 1.Should be FDA\"/CE\"/DCGI approved & Item to be Demonstrated to departmental selection committee |
| 919 | LEAD EXTRACTION |
| 920 | (D)LEAD locking device for transvenous extraction of chronically implanted pacemaker and defibrillator leads with mechanical rotating dilator 9F/11F/13F diameter with a flexible shaft and dilator sheath set .Should be FDA\"/CE\"/DCGI approved |
| 921 | (D)Lead locking device for extraction of chronically implanted leads |
| 922 | MONITOR/ECG/TMT/DEFIBRILLATOR CONSUMABLES |
| 923 | (S)SPO2 Probe Compaitable with Monitor Model : SPACE LABS.Should be FDA\"/CE\"/DCGI approved |
| 924 | (S)ECG Probe Compaitable with Monitor Model : SPACE LABS.Should be FDA\"/CE\"/DCGI approved |
| 925 | (S)BP Cuff Compaitable with Monitor Model : SPACE LABS.Should be FDA\"/CE\"/DCGI approved |
| 926 | (S)SPO2 Probe Compaitable with Monitor Model : Philips MP 30.Should be FDA\"/CE\"/DCGI approved |
| 927 | (S)ECG leads Compaitable with Monitor Model : Philips MP 30.Should be FDA\"/CE\"/DCGI approved |
| 928 | (S)NIBP cuff (Adult)Compaitable with Monitor Model : Philips MP 30.Should be FDA\"/CE\"/DCGI approved |
| 929 | (S)NIBP cuff (paediatrics)Compaitable with Monitor Model : Philips MP 30.Should be FDA\"/CE\"/DCGI approved |
| 930 | (S)BP Cuff (Adult) Compaitable with Monitor Model : Philips MP 30.Should be FDA\"/CE\"/DCGI approved |
| 931 | (S)BP Cuff (paediatrics) Compaitable with Monitor Model : Philips MP 30.Should be FDA\"/CE\"/DCGI approved |
| 932 | (S)Arterial Pressure monitoring Transducers (Disposable).Should be FDA\"/CE\"/DCGI approved |
| 933 | (S)Syringe For pressure Injector (Disposable) - Liebel Flarsheim injector 100ml.Should be FDA\"/CE\"/DCGI approved |
| 934 | (S)SPO2 Probe disposable compaitable with Multi Purpose Monitor PHILIPS A3.Should be FDA\"/CE\"/DCGI approved |
| 935 | (S)ECG Cable compaitable with Multi Purpose Monitor PHILIPS A3.Should be FDA\"/CE\"/DCGI approved |
| 936 | (S)NIBP Cuff (Adult) compaitable with Multi Purpose Monitor PHILIPS A3.Should be FDA\"/CE\"/DCGI approved |
| 937 | (S)NIBP Cuff (Child) compaitable with Multi Purpose Monitor PHILIPS A3.Should be FDA\"/CE\"/DCGI approved |
| 938 | (S)SPO2 Probe disposable compaitable with Multi Purpose Monitor AGILENT.Should be FDA\"/CE\"/DCGI approved |
| 939 | (S)ECG Cable compaitable with Multi Purpose Monitor AGILENT.Should be FDA\"/CE\"/DCGI approved |
| 940 | (S)NIBP Cuff (Adult) compaitable with Multi Purpose Monitor AGILENT.Should be FDA\"/CE\"/DCGI approved |
| 941 | (S)NIBP Cuff (Child) compaitable with Multi Purpose Monitor AGILENT.Should be FDA\"/CE\"/DCGI approved |
| 942 | (S)SPO2 Probe disposable compaitable with Multi Purpose Monitor MEC 1200.Should be FDA\"/CE\"/DCGI approved |
| 943 | (S)ECG Cable compaitable with Multi Purpose Monitor MEC 1200.Should be FDA\"/CE\"/DCGI approved |
| 944 | (S)NIBP Cuff (Adult) compaitable with Multi Purpose Monitor MEC 1200.Should be FDA\"/CE\"/DCGI approved |
| 945 | (S)NIBP Cuff (Child) compaitable with Multi Purpose Monitor MEC 1200.Should be FDA\"/CE\"/DCGI approved |
| 946 | (S)Superior Quality ECG Jelly in bottles of 250 g long lasting .Should be FDA\"/CE\"/DCGI approved |
| 947 | (S)Superior Quality ECG ECHO Jelly in bottles of 250 g long lasting .Should be FDA\"/CE\"/DCGI approved |
| 948 | (S)MORTARA ELI-250 MACHINEcable.Should be FDA\"/CE\"/DCGI approved |
| 949 | (S)MORTARA ELI 350 MACHINEcable.Should be FDA\"/CE\"/DCGI approved |
| 950 | (S)CHEST BULBS ADULT.Should be FDA\"/CE\"/DCGI approved |
| 951 | (S)CHEST BULBS PEDIATRICS.Should be FDA\"/CE\"/DCGI approved |
| 952 | (S)LIMB LEADS ADULT.Should be FDA\"/CE\"/DCGI approved |
| 953 | (S)LIMB LEADS PEDIATRICS.Should be FDA\"/CE\"/DCGI approved |
| 954 | (S) BioCare ECG recorder paper.Should be FDA\"/CE\"/DCGI approved |
| 955 | (S) BioCare ECG cable.Should be FDA\"/CE\"/DCGI approved |
| 956 | (S) Mortara ELI-250 ECG Recorder Head.Should be FDA\"/CE\"/DCGI approved |
| 957 | (S) Mortara ELI-350 ECG Recorder Head.Should be FDA\"/CE\"/DCGI approved |
| 958 | (S) Mortara ELI-350 ECG Paper..Should be FDA\"/CE\"/DCGI approved |
| 959 | (S) Mortara ELI-250 ECG Paper..Should be FDA\"/CE\"/DCGI approved |
| 960 | (S) Edan Multichannel Machine Paper.Should be FDA\"/CE\"/DCGI approved |
| 961 | (S) NIHON KODEN Multichannel Machine Paper Roll Type.Should be FDA\"/CE\"/DCGI approved |
| 962 | (S) Mortara TMT Paper.Should be FDA\"/CE\"/DCGI approved |
| 963 | (S) AG/AGCL IMPORTED PATIENT PREJELLED ELECTRODES FOR LONG-TERM MONITORING SUPERIOR QUALITY .Should be FDA\"/CE\"/DCGI approved |
| 964 | (D)Disposable Heartstart adult plus mutifunction defibrillation pads for use with the Philips defibrillator.Should be FDA\"/CE\"/DCGI approved |
| 965 | (D)Disposable pads for defibrillation / transcutaneous pacing for use with the Zoll defibrillator.Should be FDA\"/CE\"/DCGI approved |
| 966 | (D)Disposable pads for defibrillation for use with the Zoll AED.Should be FDA\"/CE\"/DCGI approved |
| 967 | (D)Reusable pads for defibrillation for use with the Zoll AED.Should be FDA\"/CE\"/DCGI approved |
| 968 | VENTILATOR CONSUMABLES |
| 969 | (S)PATIENT TUBING SYSTEM COMPATIBLE WITH MAQUET S VENTILATOR.Should be FDA\"/CE\"/DCGI approved |
| 970 | TEST KITS |
| 971 | (S)SPOT TEST KITS for HIV .Should be FDA\"/CE\"/DCGI approved |
| 972 | (S)SPOT TEST KITS for HBsAg .Should be FDA\"/CE\"/DCGI approved |
| 973 | (S)SPOT TEST KITS for HCV .Should be FDA\"/CE\"/DCGI approved |
| 974 | CLEANING/CUTTING DISPOSABLES |
| 975 | (S)StickyMats\"/Tacky Mats 1 to 30 on 30 Peel Tags, anti ststic, with Holding Stick Time : > 1000 mins, Price per box to be quoted with number of units per box.Should be FDA\"/CE\"/DCGI approved |
| 976 | Surgical Hair clipper (General Blade) - cleaning regular area battery operated for pre-operative preparational.Hair removal from body with no risk of cuts on the skin.To be supplied with suitable charger and blade.Hair clipper machine should be used in wet or dry condition and recharger for the machine should be provided.(One machine for 400 hair clipping blades) |
| 977 | Surgical Hair clipper (Sensitive blade) - cleaning sensitivearea battery operated for pre-operative preparational.Hair removal from body with no risk of cuts on the skin.To be supplied with suitable charger and blade.Hair clipper machine should be used in wet or dry condition and recharger for the machine should be provided.(One machine for 400 hair clipping blades) |
| 978 | DRAPES/COVERS/PACKING/STORE DISPOSABLE |
| 979 | (S) DISPOSABLE STERILE DRAPES FOR CORONARY ANGIOGRAPHY\"/ANGIOPLASTY COMPATIBLE WITH Bilateral FEMORAL and RADIAL APPROACHES with absorbable material.Sample to be supplied for testing |
| 980 | (S) DISPOSABLE STERILE DRAPES FOR PERMANENT PACEMAKER IMPLANTATIONL and R Pectoral Approaches.Sample to be supplied for testing |
| 981 | (S) Tissue paperbaseddisposable bed covers in continious rolls of Width \"90Cm\" for use on trolleys & Cardiac Cath Lab Tables..Sample to be supplied for testing |
| 982 | (S) DISPOSABLE STERILE ANGIOPLASTY DRAPES KITS WITHA. One Unit -DRAPE ANGIOPLASTY COMPATIBLE WITH Bilateral FEMORAL and RADIAL APPROACHES with absorbable material B. Three UnitsDISPOSABLE STERILE GOWNS C. One Unit Disosable Centre Hole towel D. One Unit Cath TrolleyDrape.Sample to be supplied for testing |
| 983 | (S) DISPOSABLE GOWN & PYJAMA SET FOR CATH LAB PROCEDURE IN DARK COLOURS - Brown/Dark Blue/ (SMALL/MEDIUM /LARGE).Sample to be supplied for testing |
| 984 | ( D) SMALL SIZE Packing material compatible with automated sealing machine for ETO sterilization of consumables..Item to be Demonstrated to departmental selection committee. |
| 985 | ( D) INTERMEDIATE SIZE Packing material compatible with automated sealing machine for ETO sterilization of consumables..Item to be Demonstrated to departmental selection committee. |
| 986 | ( D) LARGE SIZE Packing material compatible with automated sealing machine for ETO sterilization of consumables..Item to be Demonstrated to departmental selection committee. |
| 987 | (S)Disposable, sterile cover for Fluoroscopy system Image Intensifier. Should fit Image Intensifier of different sizes and should have elastic band for easy retention..Should be FDA\"/CE\"/DCGI approved & Item to be Demonstrated to departmental selection committee |
| 988 | (S)Disposable, sterile cover for Fluoroscopy system Radiation shield. Should fit Image Intensifier of different sizes and should have elastic band for easy retention..Should be FDA\"/CE\"/DCGI approved & Item to be Demonstrated to departmental selection committee |
| 989 | (D) Disposable sterile ultrasound probe cum cable \"long\" cover made of polyethene or similar translucent material with a flat end. A small pouch of sterile ultrasound jelly, elastic bands and or paper adhesive bands for binding the probe and cable to be provided as a sterile set. Different sizes that are compatible with adult and pediatric cardiac/vascular/abdominal probes to be supplied. |
| 990 | (D) Reuasable Cath-Lab Cotton Dress Shirt with three pockets and Pyjama with two pockets Large and medium Sized Light Blue Colour with the label of “ Cath-Lab JIPMER” on both the shirt and the pyjama and Size printed.Sample to be supplied |
| 991 | (S) Disposable Cath-Lab Gowns Light Blue Colour full size and elastic wrist bands with water/ blood impenetrable front and hand shielding.Should be FDA\"/CE\"/DCGI approved |
| 992 | (S)Disposable Paper-based Sterile Front Buttoned Black/ Brown/ Dark blue half sleeve shirt and pyjama for cath lab patient dress.SMALL, MEDIUM,LARGE sizes Should be FDA\"/CE\"/DCGI approved |
| 993 | (S)Compact Disk- Recordable ( CD-R) with hard shell box.Sample to be submitted to departmental selection committee. |
| 994 | (S)DVD- Recordable ( DVD-R) with hard shell box.Item to be Demonstrated to departmental selection committee. |
| 995 | (S)CD Sticker Labels with Department of Cardiology ,JIPMER Stickers, With Space for printing Angio No and CD No.Item to be Demonstrated and discussedto departmental selection committee. |
| 996 | (S)Permanent Marker Pens- Thin Script- Black.Sampleto be submittedto departmental selection committee. |
| 997 | (S)White Board Markers Black and Blue.Sampleto be submittedto departmental selection committee. |
| 998 | (D)Washable and Autoclavable Cut Shoes (Clogs) Specially designed for wearing in Cathlabs/Operation rooms /ICU\"s wear slippers at least 12 inch foot length.(roomy fit). should have non collapsible sole to support the arch of foot. The brochure mentioning the details of the product should be submitted . Mention various sizes available.(Small, Medium, Large and Extra large).Item to be Demonstrated to the departmental selection committee |
| 999 | MONITORING DEVICES - NON CONSUMABLES |
| 1000 | ( D) BATTERY OPERATED AUTOMATED DIGITAL BP APPARATUS with ADULT,LARGE ADULT and PEDIATRIC CUFFS with 3 yr warranty.Item to be Demonstrated to departmental selection committee. |
| 1001 | ( D ) DIGITAL BP APPARATUS HEAVY DUTY, with ADULT,LARGE ADULT and PEDIATRIC CUFFS RUNNING IN AC POWER with rechargable Lithium ion batters FOR USE IN OPD AND WARD with 3 yr warranty.Item to be Demonstrated to departmental selection committee. |
| 1002 | ( D ) DIGITAL BP, SpO2, Respiratory Rate, TemperatureMeasuring APPARATUS HEAVY DUTY, with ADULT, LARGE ADULT and PEDIATRIC CUFFS RUNNING IN AC POWER with rechargeable Lithium-ion Battery FOR USE IN OPD AND WARD3 yr warranty.Item to be Demonstrated to the departmental selection committee. |
| 1003 | (D) DIGITAL Automated BP apparatus for use with TMT machine with automatic noise detection and artefact cancellation and ability for ECG gating |
| 1004 | ( D)DIGITAL WEIGHING SCALE FOR PATIENT WEIGHT with 3 yr warranty.Item to be Demonstrated to departmental selection committee. |
| 1005 | ( D) Battery Operated Pocket Sized SpO2 Probes.Item to be Demonstrated to departmental selection committee. |
| 1006 | (D) Digital Stadiometer for height measurement. |
| 1007 | (D) Temperature and Humidity monitors for Cathlabs and ICU. Should have maximum and minimum values for 24 hours on display and ability to store 30 days data for export. |
| 1008 | (D) Dual zone Temperature monitors for Refrigerators for monitoring freezer and cabin temperatures. Should have maximum and minimum values for 24 hours on display and ability to store 30 days data for export. |
| 1009 | (D)MULTIPARAMETER MONITORS ECG, SPO2,NIBP with 3yr warrranty and2 sets of cables.Item to be Demonstrated to the departmental selection committee. |
| 1010 | ( D) SYRINGE INFUSION PUMPS with 3 yr warranty.Item to be Demonstrated to departmental selection committee. |
| 1011 | ( D) OT LIGHT- FLOOR MOUNTED, LED SOURCE , Brightness and Focus ADJUSTABLE with 3 yr warranty.Item to be Demonstrated to departmental selection committee. |
AI Tender Summary
Tender Timeline
Tender Published
Tender notice published.
CompletedCorrigendum-1 Issued
Clarifications on tender conditions and amendments issued.
CompletedBid Submission Deadline
Online submission via eProcurement portal.
CompletedBid Opening Date
Technical bids will be opened and evaluated.
CompletedTender Documents
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