Tender For Cardiology And Nephrology Consumable Item , Drug Eluting Stents, Pacemakers, Ptmc Balloon And Other Consumable Items , Group – A (Interventional Cardiology) , Radial Introducer Needle18g, 70Mm Length & 20G, 40Mm – Usfda/Ce/Dcgi Approved ?Tip- Sharp Half-Moon Bevel Shape Diamond Cutting. 18 G 7 Cm 20G 4 Cm. , Iv Canula - 20G, /21G 3.2 Cm And 4 Cm – Usfda/Ce/Dcgi Approved ?Ultrasharp Electropolished Pointed Tip. Thin-Walled Construction, Radiopaque In Nature Cannula Made Up Of Clear Polyurethane. Hub Shape Round Mini Wings/No Wings With Flash Plug. 20G,21G 3.2 Cm And 4 Cm , Trans Radial Introducer Kit With Puncture Needle - 4F-7F – 7/10/15/25 Cm, Usfda/Pmda Approved ?Sizes - 4 – 7 French, Length – 7/10/15/25 Cm ?Pack Must Include 20 G/45Mm Entry Needle, 0.025-Inch X 45/80 Cm Hydrophilic Mini Guidewire. ?Must Have Etfe Sheath Tubing, Dilator Tube Should Be Made Up Of Polypropylene And Should Have Silicon Coating. ?Should Contain Haemostatic Crosscut Valve To Prevent Back Leak Of Blood And Aspiration Of Air; With Integrated Side Arm With Attached 3-Way Stopcock. ?With Suture Eye For Securing Sheath, Kink Resistant, With Snap-On Dilator-Hub Lock Mechanism To Prevent Its Back-Out. , Trans Radial Introducer Kit With Puncture Needle - 4F-7F – 7/10/15/25 Cm, Ce/Dcgi Approved ?Sizes - 4 – 7 French, Length – 7/10/15/25 Cm ?Pack Must Include 20 G/45Mm Entry Needle, 0.025-Inch X 45/80 Cm Hydrophilic Mini Guidewire ?Must Have Etfe Sheath Tubing, Dilator Tube Should Be Made Up Of Polypropylene And Should Have Silicon Coating. ?Should Contain Haemostatic Crosscut Valve To Prevent Back Leak Of Blood And Aspiration Of Air; With Integrated Side Arm With Attached 3-Way Stopcock. ?With Suture Eye For Securing Sheath, Kink Resistant, With Snap-On Dilator-Hub Lock Mechanism To Prevent Its Back-Out. , Radial Introducer Kit - Hydrophilic Cto Approachable Slender Profile 4F-7F, 6.5F -Length - 7 Cm, 11Cm, 15Cm, 25Cm – Ce Approved ?Sizes - 4 – 7 French. Must Include 6.5F Special Sheath, Length - 7 Cm, 11Cm, 15Cm, 25Cm. ?Pack Must Include 22G/45Mm Plastic Entry Needle, 0.025-Inch X 45/80 Cm Hydrophilic Mini Guidewire. ?Must Have Metal Mesh Braided Structure ?Must Have 3 Layer Sandwich Of Ptfe Sheath Tubing With Pebax Inner Layer And Ss Braid, Dilator Tube Should Be Made Up Of Polypropylene And Should Have Silicon Coating. ?Should Contain Haemostatic Crossover Valve To Prevent Back Leak Of Blood And Aspiration Of Air; With Integrated Side Arm With Attached 3-Way Stopcock. ?With Suture Eye For Securing Sheath, Kink Resistant, With Rotation-Hub Lock Mechanism To Prevent Its Back-Out During Insertion , Slender Profile Hydrophilic Sheath 5-7 F (10, 16, Cm) - Usfda/Pmda Approved ?Must Have Unique Thin Wall Technology Reducing The Outer Diameter By 1 Fr Size Whilst Maintaining The One Size Lager Inner Diameter. 5Fr In 4, 6Fr In 5, 7Fr In 6 Profile. ? Must Have 7Fr Sheath With Outer Diameter Of 2.8Mm, 6Fr With Od Of 2.46 Mm & 5Fr With Od Of 2.13Mm. ?Hydrophilic M Coating With 20/21G Surflash Needle And Tif Tip Technology Which Provide Optimal Tapering Design. , Femoral Introducer Kit 4-11F (10, 16 & 25 Cm) - Usfda/Pmda Approved • Sizes - 4 – 11 French, Length – 10, 16 & 25 Cm • Pack Must Include 18 G/20G, Surflash Entry Needle, 0.035- Or 0.025-Inch X 45 Cm Mini Plastic Guidewire • Must Have Etfe Sheath Tubing, Dilator Tube Should Be Made Up Of Polypropylene And Should Have Silicon Coating. • Should Contain Haemostatic Crosscut Valve To Prevent Back Leak Of Blood And Aspiration Of Air; With Integrated Side Arm With Attached 3-Way Stopcock. • With Suture Eye For Securing Sheath, Kink Resistant, With Snap-On Dilator-Hub Lock Mechanism To Prevent Its Back-Out During Insertion , Femoral Introducer Kit 4-11F (10, 16 & 25 Cm) – Ce/Dcgi Approved ?Sizes - 4 – 11 French, Length – 10, 16 & 25 Cm ?Pack Must Include 18 G/20G, Surflash Entry Needle, 0.035- Or 0.025-Inch X 45 Cm Mini Plastic Guidewire ?Must Have Etfe Sheath Tubing, Dilator Tube Should Be Made Up Of Polypropylene And Should Have Silicon Coating. ?Should Contain Haemostatic Crosscut Valve To Prevent Back Leak Of Blood And Aspiration Of Air; With Integrated Side Arm With Attached 3-Way Stopcock. ?With Suture Eye For Securing Sheath, Kink Resistant, With Snap-On Dilator-Hub Lock Mechanism To Prevent Its Back-Out During Insertion , Femoral Introducer Kit - Hydrophilic Cto Approachable Slender Profile 4F-18F, Length - 11Cm, 15Cm, 25Cm – Ce Approved ?Sizes - 4 – 18 French. Length - 11Cm, 15Cm, 25Cm ?Pack Must Include 18G/70 Mm Plastic Entry Needle, 0.038-Inch X 45/80 Cm & .035 For 4F Hydrophilic Mini Guidewire. ?Must Have Metal Mesh Braided Structure ?Must Have 3 Layer Sandwich Of Ptfe Sheath Tubing With Pebax Inner Layer And Ss Braid, Dilator Tube Should Be Made Up Of Polypropylene And Should Have Silicon Coating. ?Should Contain Haemostatic Crossover Valve To Prevent Back Leak Of Blood And Aspiration Of Air; With Integrated Side Arm With Attached 3-Way Stopcock. ?With Suture Eye For Securing Sheath, Kink Resistant, With Rotation-Hub Lock Mechanism To Prevent Its Back-Out During Insertion , Braided Long Sheath – 6-8F – 45Cm - Usfda/Pmda Approved ?Diameter 6,7,8F And Length 45Cm. Atraumatic Tip For Carotid & Distal Procedures ?Haemostatic Valves (Cross Cut Valve & Tbv- Detachable Valves For Thrombus Management) ?Gold Coil Marker - For Distal Visibility ?Ptfe Coating - Seamless Device Transition, Distal Hydrophilic Coated For Navigability ?Nylon Outer Layer With Reinforced Stainless-Steel Coil - Helps In Smooth & Anti-Kink Effect , Braided Long Sheath – 6-8F – 45Cm – Ce/Dcgi Approved ?Diameter 6,7,8F And Length 45Cm. Atraumatic Tip For Carotid & Distal Procedures ?Haemostatic Valves (Cross Cut Valve & Tbv- Detachable Valves For Thrombus Management) ?Gold Coil Marker - For Distal Visibility ?Ptfe Coating - Seamless Device Transition, Distal Hydrophilic Coated For Navigability ?Nylon Outer Layer With Reinforced Stainless-Steel Coil - Helps In Smooth & Anti-Kink Effect , Braided Long Sheath – 6-8F – 65Cm - Usfda/Pmda Approved ?Diameter 6,7,8F And Length 65Cm. Atraumatic Tip For Carotid & Distal Procedures ?Haemostatic Valves (Cross Cut Valve & Tbv- Detachable Valves For Thrombus Management) ?Gold Coil Marker - For Distal Visibility ?Ptfe Coating - Seamless Device Transition, Distal Hydrophilic Coated For Navigability ?Nylon Outer Layer With Reinforced Stainless-Steel Coil - Helps In Smooth & Anti-Kink Effect , Braided Long Sheath – 6-8F – 65Cm – Ce/Dcgi Approved ?Diameter 6,7,8F And Length 65Cm. Atraumatic Tip For Carotid & Distal Procedures • Haemostatic Valves (Cross Cut Valve & Tbv- Detachable Valves For Thrombus Management) • Gold Coil Marker - For Distal Visibility • Ptfe Coating - Seamless Device Transition, Distal Hydrophilic Coated For Navigability • Nylon Outer Layer With Reinforced Stainless-Steel Coil - Helps In Smooth & Anti-Kink Effect , Braided Long Sheath – 6-8F – 90Cm - Usfda/Pmda Approved ?Diameter 6,7,8F And Length 90Cm. Atraumatic Tip For Carotid & Distal Procedures ?Haemostatic Valves (Cross Cut Valve & Tbv- Detachable Valves For Thrombus Management) ?Gold Coil Marker - For Distal Visibility ?Ptfe Coating - Seamless Device Transition, Distal Hydrophilic Coated For Navigability ?Nylon Outer Layer With Reinforced Stainless-Steel Coil - Helps In Smooth & Anti-Kink Effect , Braided Long Sheath – 6-8F – 90Cm – Ce/Dcgi Approved ?Diameter 6,7,8F And Length 90Cm. Atraumatic Tip For Carotid & Distal Procedures ?Haemostatic Valves (Cross Cut Valve & Tbv- Detachable Valves For Thrombus Management) ?Gold Coil Marker - For Distal Visibility ?Ptfe Coating - Seamless Device Transition, Distal Hydrophilic Coated For Navigability ?Nylon Outer Layer With Reinforced Stainless-Steel Coil - Helps In Smooth & Anti-Kink Effect , Braided Long Sheath – 8-18F – All Length – Ce/Dcgi Approved ?Diameter 8-18F And All Length. Atraumatic Tip For Carotid & Distal Procedures ?Haemostatic Valves (Cross Cut Valve & Tbv- Detachable Valves For Thrombus Management) ?Gold Coil Marker - For Distal Visibility ?Ptfe Coating - Seamless Device Transition, Distal Hydrophilic Coated For Navigability ?Nylon Outer Layer With Reinforced Stainless-Steel Coil - Helps In Smooth & Anti-Kink Effect , Hydrophilic Guidewire (Length - 150) With Mcoat/Hydrocoat Technology – Pmda/Ce Approved ?Standard Tip & .035, .032, .038, .025. .018 Diameter & 150 Cm Length - Straight / Angled / 1.5Mm J Shape ?Tapered Tip, Single Nitinol Core Alloy, Tungsten-Infused Polyurethane Jacket ?Hydrophilic Polymer Coat. One Piece Construction & Radiopaque Polyurethane Jacket. , Hydrophilic Guidewire (Length - 150) With Mcoat/Hydrocoat Technology – Dcgi Approved ?Standard Tip & .035, .032, .038, .025. .018 Diameter & 120 Cm & 150 & 180 Cm Length - Straight / Angled / 1.5Mm J Shape, Straight A, S, R-1.5Mmj, R-3Mmj In Standard And Stiff Support Level ?Tapered Tip, Single Nitinol Core Alloy, Tungsten-Infused Polyurethane Jacket ?Hydrophilic Polymer Coat. One Piece Construction & Radiopaque Polyurethane Jacket. , Hydrophilic Guidewire (Length - 180) With Mcoat/Hydrocoat Technology – Pmda/Ce Approved ?Standard Tip & .035, .032, .038, .025. .018 Diameter & 180 Cm Length - Straight / Angled ?Tapered Tip, Single Nitinol Core Alloy, Tungsten-Infused Polyurethane Jacket ?Hydrophilic Polymer Coat. One Piece Construction & Radiopaque Polyurethane Jacket. , Hydrophilic Guidewire (Length - 260) With Mcoat/Hydrocoat Technology – Pmda/Ce Approved ?Standard Tip & .035, .032, .038, .025. .018 Diameter & 260 Cm Length - Straight / Angled ?Tapered Tip, Single Nitinol Core Alloy, Tungsten-Infused Polyurethane Jacket ?Hydrophilic Polymer Coat. One Piece Construction & Radiopaque Polyurethane Jacket. , Hydrophilic Guidewire (220 & 260) With Mcoat/Hydrocoat Technology – Dcgi Approved • Standard Tip & .035, .032, .038, .025. .018 Diameter & 220 Cm & 260 Cm Length - Straight / Angled / 1.5Mm J Shape, Straight A, S, R-1.5Mmj, R-3Mmj In Standard And Stiff Support Level • Tapered Tip, Single Nitinol Core Alloy, Tungsten-Infused Polyurethane Jacket • Hydrophilic Polymer Coat. One Piece Construction & Radiopaque Polyurethane Jacket. , Extra Stiff - Hydrophilic Guidewire -150 Cm Usfda/Pmda Approved • 0.035, .032, .038, .025, .018 Diameter And 150 Cm Length - Straight / Angled -Half Stiff And Stiff, Extra Stiff • With Mcoat Technology Tapered Tip, Single Nitinol Core Alloy, Tungsten-Infused Polyurethane Jacket • Hydrophilic Polymer Coat. One Piece Construction & Radiopaque Polyurethane Jacket. , Extra Stiff - Hydrophilic Guidewire -260 Cm Usfda/Pmda Approved • 0.035, .032, .038, .025, .018 Diameter And 150 Cm Length - Straight / Angled -Half Stiff And Stiff, Extra Stiff • With Mcoat Technology Tapered Tip, Single Nitinol Core Alloy, Tungsten-Infused Polyurethane Jacket • Hydrophilic Polymer Coat. One Piece Construction & Radiopaque Polyurethane Jacket. , Ptfe Guidewire 150 Cm - Usfda/Pmda Approved ?150Cm, 175 Cm Of Lengths & 0.018 To 0.038 Diameter With Silicon Coated Tip. ?Silicon Coated Tip With Choice Of Stainless-Steel Core Or Nitinol Core, ?Should Be Available Fixed As Well As Movable Core. , Ptfe Guide Wire – 150 Cm – Ce/Dcgi Approved ?Should Be Available In 0.025, 0.032, 0.035 & 0.038 Inches, 150 Cm Long, Straight & J-Shaped Tip ?Should Be Available In Variable Lengths Of Flexible/Floppy End, Variable J Tip Sizes ?Should Be Available Fixed As Well As Movable Core. , Ptfe Guidewire – 260 Cm - Usfda/Pmda Approved ?260 Cm Of Lengths & 0.018 To 0.038 Diameter With Silicon Coated Tip. ?Silicon Coated Tip With Choice Of Stainless-Steel Core Or Nitinol Core, ?Should Be Available Fixed As Well As Movable Core. , Ptfe Guide Wire – 260 Cm – Ce/Dcgi Approved ?Should Be Available In 0.025, 0.032, 0.035 & 0.038 Inches, 150 Cm Long, Straight & J-Shaped Tip ?Should Be Available In Variable Lengths Of Flexible/Floppy End, Variable J Tip Sizes ?Should Be Available Fixed As Well As Movable Core. , Amplatz Super-Stiff Guide Wire - 260 – Usfda/Ce/Dcgi Approved ?Should Be Available In 0.035- And 0.038-Inches Size, 260/300 Cm Long, Straight Or J-Shaped Tip ?Should Be Available Fixed As Well As Movable Core. , Double Curve Extra Stiff Guide Wire – Landerquist Type – Regular Length , Double Curve Extra Stiff Guide Wire – Landerquist Type – 260Cm/300Cm , Pre-Shaped – Tavi Support Wire – Usfda Approved ?Outer Diameter: 0.035” (0.889 Mm), Length: 275 Cm ?Core Material: Stainless Steel With Lubrigree Ptfe Coating ?Unique Product Dimensions By Curve Size - Extra Small, Small, Large Curve , Radial Angiographic Catheter – Tig Curve (4-6F) - Usfda/Pmda -Approved ?Sizes - 4F, 5F, 6F, Shapes - Tig/3.5 Jacky/4-Sarah ?Two-Layer Construction, Double Braided Stainless-Steel Two-Ply Mesh Sandwiched Between Layers Of Polyurethane And Polyamide Elastomers. ?Must Have The Shaft Inner Layer And Outer Layer Contain Barium Sulphate With 32 Strands Of Stainless-Steel Braid ?Must Have Anti-Kinking Protector Sleeve, With Non-Braided Tip Shaft (Distal -2 Cm). ?Must Have Inner Diameter Of 4F = 1.03Mm, 5F= 1.20Mm, 6F = 1.30Mm , Radial Angiographic Catheter Hydrophilic – Tig Curve (4-6F) - Dcgi Approved ?Length - 80Cm / 100Cm / 110Cm / 130Cm, Sizes - 4F, 5F, 6F ?Must Have Triple-Layer Construction, Double Braided Stainless-Steel Two-Ply Mesh Sandwiched Between Layers Of Nylon And Pebax. ?Must Have Anti-Kinking Protector Sleeve, With Uncoated Non-Braided Tip Shaft (Distal -2 Cm) ?Must Have Inner Diameter Of 4F = 1.05Mm, 5F= 1.20Mm, 6F = 1.47Mm With 1000Psi Flow Rate. , Radial Angiographic Catheter Hydrophilic – Tig Curve (4-6F) - Dcgi Approved ?Length - 80Cm / 100Cm / 110Cm / 130Cm, Sizes - 4F, 5F, 6F ?Must Have Triple-Layer Construction, Double Braided Stainless-Steel Two-Ply Mesh Sandwiched Between Layers Of Nylon And Pebax. ?Must Have Anti-Kinking Protector Sleeve, With Uncoated Non-Braided Tip Shaft (Distal -2 Cm) ?Must Have Inner Diameter Of 4F = 1.05Mm, 5F= 1.20Mm, 6F = 1.47Mm With 1000Psi Flow Rate. , Femoral Diagnostic Catheter: 4 -6 Fr (Jl, Jr, Al, Ar, Pigtail) - Ce Approved ? Shapes - Jl, Jr, Al, Ar,Pigtail ? Triple-Layer Construction, Double Braided Stainless-Steel Two-Ply Mesh Sandwiched Between Layers Of Nylon And Pebax. ? Inner Diameter Of 4F = 1.04Mm, 5F= 1.20Mm, 6F = 1.47Mm With 1000Psi Flow Rate. ? Catheter Should Have Slender Profile Ultra-Thin Wall That Creates Large Lumen. ? Catheter Should Have Anti-Kinking Protector, With Uncoated Non-Braided Tip Shaft (Distal -2 Cm). , Femoral Diagnostic Catheter: 4 -6 Fr (Jl, Jr, Al, Ar, Im, Pigtail, Mp) - Usfda/Pmda -Approved ?Transfemoral Catheter Shapes Jl, Jr, Al, Ar, Im, Pigtail, Mp ?Braided Catheter With Stainless Steel Mesh Technology. ?Inner Diameter Of 4Fr =1.03Mm ,5Fr = 1.20Mm, 6Fr = 1.30Mm Or More Resulting In Higher Flow Rates. ?The Shaft Inner Layer And Outer Layer Should Contain Barium Sulphate With 32 Strands Of Stainless-Steel Braid ?Catheter Should Have Ultra-Thin Wall That Creates Large Lumen. ?Catheter Should Have Anti-Kinking Protector, With Non-Braided Tip Shaft (Distal -2 Cm). , Judkins Catheter (Jr & Jl) – 4 – 6 Fr ?Size - 4 French/5 French /6 French Size , Amplatz Catheter – Al & Ar – 4 6 Fr ?Size - 4 French/5 French /6 French , Multipurpose Catheter (Mp) 4-6 Fr ?Size - 4 French/5 French /6 French Size , Pigtail Catheter – 4 -6 Fr ?Size – 4 – 6 French , Angiographic Sizing Pigtail Catheter 5F/ 6F/ 7F – ?Size – 5 F – 7 F , Internal Mammary Catheter – 4 -6 Fr ?Size - 4 French/5 French /6 French In Various Standard Curves And Lengths. , By-Pass Graft Catheter ?Size - 4 French/5 French /6 French In Various Standard Curves And Lengths. , Nih Catheter - ?4 French/5 French /6 French/7 French/8French In Various Standard Curves And Lengths. , Cournard Catheter ?4 French/5 French /6 French/7 French/8French In Various Standard Curves And Lengths. , Diagnostic Catheters For Neonatal Use - 3- ‘French’ ?Pigtail, Judkins, Multipurpose, Cobra And Other Diagnostic Catheters Of 3 Fr. Size ?Varying Lengths And Shapes , Drug Delivery/Infusion Catheter , Coronary Probing Catheter , Coronary Perfusion Catheter , Coronary Trapeer Catheter , Swan Ganz Catheter - Us Fda Approved- 6F/7F , Swan Ganz Catheter – Ce/Dcgi Approved- 6F/7F , Special Swan Ganz Catheter ?Sizes - 4F, 5F, 6F And 7F And 8 Fr ?4 F Catheter Should Allow The Passage Of At Least 0.021, 5 F – 0.025, 6 F – 0.035 And 7 F, 8F – 0.038-Inch Hydrophilic Guide Wire Catheter Should Be Tapered At Tip To Ensure Uniform Diameter Of The Whole Catheter, 10 Cm Marking Along The Catheter Body. , Balloon Tipped Angiography Catheter , Berman Catheter ?Must Be Available In 4F, 5F, 6F And 7F Sizes ?Should Have 6-8 Holes Proximal To The Balloon For Dye Injection ?Catheter Should Be Tapered At Tip To Ensure Uniform Diameter Of The Whole Catheter, 10 Cm Marking Along Catheter , Reverse Berman Catheter ?Should Be Available In 4F, 5F, 6F & 7F Sizes ?Catheter Should Be Tapered At Tip To Ensure Uniform Diameter Of The Whole Catheter ?Should Have Holes Proximal To The Balloon For Dye Injection ?Should Have A Hole At The Proximal Tip To Allow The Passage Over The Wire , Pigtail Catheter (Pediatric) ?Sizes 3 French/ 4 French/ 5 French/ 6 French ?Smaller Length For Neonatal And Pediatric Use , Special Judkins Coronary Catheter With 2.5 Cm Curve (Pediatric) ?Sizes - 4 F/ 5 F/ 6 F , Angiographic Double Leumen Tracking Catheter – 4 F/5F/ 6F , Renal Double Curve Catheter ?In Various Standard Lengths And Curves , Head Hunter Catheter ?In Various Standard Lengths And Curves ?035-038 Compatible ?100 Cm Long , Simmons/ Sidewinder Catheter ?In Various Standard Lengths And Curves ?035-038 Compatible ?100 Cm Long , Preshaped Catheter For Uterine Artery Embolisation ?In Various Standard Lengths And Curves , Vertebral Catheter ?In Various Standard Lengths And Curves , Coeliac Axis Catheter ?In Various Standard Lengths And Curves , Shepherd’S Hook Catheter ?In Various Standard Lengths And Curves , Vtk Diagnostic Catheter ?In Various Standard Lengths And Curves 5F, 6F Size , 3D Space Rca Angiographic Catheter , Adjustable Hemostasis Valve For Catheters – Usfda Approved ?Should Meet Highest Medical Industrial Standards Click-On ?Quality Certification Should Be Provided From Authorized Agencies. , Adjustable Hemostasis Valve For Catheters - Ce Approved ?Should Meet Highest Medical Industrial Standards ?Quality Certification Should Be Provided From Authorized Agencies. , Adjustable Hemostasis Valve For Catheters - Dcgi Approved ?Should Meet Highest Medical Industrial Standards ?Quality Certification Should Be Provided From Authorized Agencies. , Hemostasis Valve - 8 Fr. Inner Lumen – Usfda Approved ?Star-Shaped Seal With Rotolock , Hemostasis Valve - 8 Fr. Inner Lumen – Ce Approved ? Star-Shaped Seal With Rotolock , Hemostasis Valve - 8 Fr. Inner Lumen – Dcgi Approved ? Star-Shaped Seal With Rotolock , Ptca Pressure Console – Usfda Approved , Ptca Pressure Console – Ce Approved , Ptca Pressure Console – Dcgi Approved , Angioplasty Pressure Diversion Module (Dual-Pathway) – Usfda Approved , Angioplasty Pressure Diversion Module (Dual-Pathway) -Ce Approved , Angioplasty Pressure Diversion Module (Dual-Pathway) -Dcgi Approved , Angioplasty Pressure Diversion Module (Tri-Pathway) – Usfda Approved , Angioplasty Pressure Diversion Module (Tri-Pathway) – Ce Approved , Angioplasty Pressure Diversion Module (Tri-Pathway) – Dcgi Approved , High – Presure Injector Lines - Dcgi Approved ? Should Be Available In Various Lengths ? Should Have Male And Female Luer Locks ? Should Be Transparent And Kink Resistant ? Should Be Able To Take High Pressure Of Angiographic Injections , Disposable Ecg Electrodes For Adults - Us Fda Approved ? Adult Diaphoretic Foam Electrodes. ? Should Be Pre-Gelled, Peel And Stick Electrode With Excellent Adhesion ? Should Have No Residue Once Removed ? Should Conform To Or Exceed The Highest Industrial Standard For Ecg Electrodes,Ation , Special Radiolucent Disposable Ecg Electodes For Adults – Dcgi Approved ? Radiolucent Electrodes For Electro-Physiologic Studies ? Wet Gel Electrodes, Should Be Porous And Breathable ? Should Conform To Or Exceed The Highest Industrial Standard For Ecg Electrodes, ? Quality Certification From Authorized Agencies To Be Provided , Syringe For Pressure Injector Installed In Cath Lab ? Should Be Compatible With Existing Machines At Cath Lab, Gmck , High-Pressure – Contrast Delivery Injector – With Luer Lock Mechanism- 10 Ml , High-Pressure – Contrast Delivery Injector – With Luer Lock Mechanism- 20 Ml , Arterial Pressure Monitor Lines (100, 150 & 200 Cm Long) ?Should Be Available In Sizes Of 100, 150 & 200 Cm Should Have Male Luer Lock Connection At One End And A Female Luer Lock Connection At The Other End , High-Fidelity Pressure Monitoring Extension Line – 200 ? Medical-Grade Pvc Or Dehp-Free Polyethylene, Male And Female Luer Lock Connectors, ? Must Be Dehp-Free (Diethylhexyl Phthalate-Free) And Latex-Free.Pressure Ratings – 1200 Psi , Disposable Transducers For Invasive Pressure Monitoring Compatible With Available System In Cath Lab In Gmck Hospital ?Disposable Transducers For Invasive Pressure Monitoring ?Should Be Compatible With Available System In Cath Lab (Iabp – Data Scope & Cath Lab Transducer) And Iccu At Gmck ?Should Meet Highest Medical Industrial Standards ?Quality Certification Should Be Provided Form Authorized Agencies , Domes For Transducer For Invasive Pressure Monitoring - Dcgi Approved ?Should Be Compatible With Existing Available System At Cath Lab And Ccu At Gmck ?Should Meet Or Exceed Highest Standards ?Quality Certification From Authorized Agencies To Be Provided , Ptca Inflation Device - Us Fda Approved ?Efficient Locking System To Maintain High Pressure ?Rapid Inflation And Deflation, Clear Barrel For Easy Visualization Of De-Bubbling ?Luminescent Analog Pressure Gauge (Up To 30 Atm), 20/30 Inflation Device Registers Pressures Up To 30 Atmospheresergometric And Use Friendly Hand Held Design. , Ptca Inflation Device - Ce Approved ?Efficient Locking System To Maintain High Pressure ?Rapid Inflation And Deflation, Clear Barrel For Easy Visualization Of De-Bubbling ?Luminescent Analog Pressure Gauge (Up To 30 Atm),20/30 Inflation Device Registers Pressures Up To 30 Atmospheres Ergometric And Use Friendly Hand Held Design. , Ptca Inflation Device - Dcgi Approved ?Efficient Locking System To Maintain High Pressure ?Rapid Inflation And Deflation, Clear Barrel For Easy Visualization Of De-Bubbling ?Luminescent Analog Pressure Gauge (Up To 30 Atm), 20/30 Inflation Device Registers Pressures Up To 30 Atmospheresergometric And Use Friendly Hand Held Design. , Y-Connector – Push Pull Mechanism - Us Fda/Pmda Approved ?9F Bore Size For Usage With A Variety Of Devices ?Should Accommodate Virtually All Interventional Devices ?Luer Connector At The Guiding Catheter End, Rotating Adapter At The Guiding Catheter End ?Should Have Bleed Back Safety Mechanism, Stepwise Control For Open, Semi-Open And Closed Position , Y-Connector– Push Pull Mechanism – Ce/Dcgi Approved ?9F Bore Size For Usage With A Variety Of Devices ?Should Accommodate Virtually All Interventional Devices ?Luer Connector At The Guiding Catheter End, Rotating Adapter At The Guiding Catheter End ?Should Have Bleed Back Safety Mechanism, Stepwise Control For Open, Semi-Open And Closed Position , Y-Connector – Push Click Mechanism –180 Psi Pressure Sustenace - Dcgi Approved ?9F Bore Size For Usage With A Variety Of Devices, With 180 Psi Of Pressure Sustenance. ?Should Accommodate Virtually All Interventional Devices ?Luer Connector At The Guiding Catheter End, Rotating Adapter At The Guiding Catheter End ?Should Have Bleed Back Safety Mechanism, Stepwise Control For Open, Semi-Open And Closed Position , Y-Connector – Push Click Mechanism - 300 Psi Pressure Sustenace –Dcgi Approved ?9F Bore Size For Usage With A Variety Of Devices, With 300 Psi Of Pressure Sustenance. ?Should Accommodate Virtually All Interventional Devices ?Luer Connector At The Guiding Catheter End, Rotating Adapter At The Guiding Catheter End ?Should Have Bleed Back Safety Mechanism, Stepwise Control For Open, Semi-Open And Closed Position , Y- Connector Kit – Push Pull Mechanism - Stepwise Control For Open, Semi-Open And Closed Position (Okay – 2 Type) - Us Fda / Ce Approved ?Should Accommodate Virtually All Interventional Devices ?Luer Connector At The Guiding Catheter End, Rotating Adapter At The Guiding Catheter End ?Should Have Bleed Back Safety Mechanism , W-Connector - Bifurcation Ptca – Usfda/Ce//Dcgi Approved ?Two Ports For Insertion Of Two Ptca Balloons Or One Balloon And One Other Part At The Same Time ?Luer Connector At The Guiding Catheter End, Rotating Adapter At The Guiding Catheter End , Manifold With Attached Tubings (Angio Kit) With 3 Port Left-Off /Right Off Orientation - Us Fda/Ce/Dcgi Approved ? Pressure Integrity - 250 Pascal Per Square Inches -500 Pascal Per Square Inches Rating And Wide Port Spacing. Clear Polycarbonate Body ? Integrated Pre-Flushed Transducer Port ? Minimum Flow Rate Of 85 Ml/Sec At 500 Psi. The Design Must Minimize Turbulence And Air Entrapment, Evidenced By An Airless Rotator Mechanism For Enhanced Patient Safety ? Three Side Port Manifold, One Connector Tubing For Connecting Manifold To Tuohy Borst ? One Luer Lock Control Syringe (10 Or 12 Ml) For Contrast Injection ? Two Large Bore Tubing (With Flow Regulating Knob) For Withdrawing Contrast & Saline One 3 Way Stop-Cock ? Color Coded Manifold With Left-Off /Right Off Orientation. , Manifold With Attached Tubings (Angio Kit) With 2 Port Left-Off /Right Off Orientation – Usfda/Ce/Dcgi Approved ? Pressure Integrity - 250 Pascal Per Square Inches -500 Pascal Per Square Inches Rating And Wide Port Spacing. Clear Polycarbonate Body ? Integrated Pre-Flushed Transducer Port ? Minimum Flow Rate Of 85 Ml/Sec At 500 Psi. The Design Must Minimize Turbulence And Air Entrapment, Evidenced By An Airless Rotator Mechanism For Enhanced Patient Safety ? Two Side Port Manifold, One Connector Tubing For Connecting Manifold To Tuohy Borst ? One Luer Lock Control Syringe (10 Or 12 Ml) For Contrast Injection ? Two Large Bore Tubing (With Flow Regulating Knob) For Withdrawing Contrast & Saline One 3 Way Stop-Cock ? Color Coded Manifold With Left-Off /Right Off Orientation. , Guiding Catheter With Special Extra Backup Curve Length (Abu 3.0, 3.25, 3.5, 3.75, 4.0) – Ce Approved ? Must Have (Abu 3.0, 3.25, 3.5, 3.75, 4.0) And Must Include 6.5 French Catheter ? Must Have Triple Layered Ss Braided Sandwich Structure With Outer Polymer Blend Layer & Inner Ptfe Layer ? Must Have Flat Wire Braided Structure, Should Have Uncoated And Non-Braided Atraumatic Soft Tip ? Must Have Various Tip Shapes And Curves – Extrabackup Left, Jl&Jr, Al&Ar, Mp ? Should Have Od Of 6F, 6.5F, 7F-8F. , Special 6.5 Introducer & 6.5F Guiding Catheter (Combo) – For Tri Procedures – Ce Approved ? Must Have Triple Layered Ss Braided Sandwich Structure With Outer Polymer Blend Layer & Inner Ptfe Layer ? Must Have Flat Wire Braided Structure ? Should Have Uncoated And Non-Braided Atraumatic Soft Tip ? Must Have Various Tip Shapes And Curves – Extrabackup Left, Jl&Jr, Al&Ar, Mp , Radial Guiding Catheter Both Curve -Us Fda Approved ? Should Be Braided With Low Friction Inner Layer ? Should Have Atraumatic Soft Tip ? Should Be Available In Various Tip Shapes And Curves For Access To Different Parts Of The Peripheral Vasculature, Including Renal Double Curve, Cobra, Multi – Purpose And Other Shapes ? Should Have Od Of 6F-8F Available ? Should Have The Largest Id For Each Od ? Should Have Lengths Ranging From 55-90 Cm , Radial Guiding Catheter Both Curve -Ce Approved ? Should Be Braided With Low Friction Inner Layer ? Should Have Atraumatic Soft Tip ? Should Be Available In Various Tip Shapes And Curves For Access To Different Parts Of The Peripheral Vasculature, Including Renal Double Curve, Cobra, Multi – Purpose And Other Shapes ? Should Have Od Of 6F-8F Available ? Should Have The Largest Id For Each Od ? Should Have Lengths Ranging From 55-90 Cm , Radial Guiding Catheter Both Curve -Dcgi Approved ? Should Be Braided With Low Friction Inner Layer ? Should Have Atraumatic Soft Tip ? Should Be Available In Various Tip Shapes And Curves For Access To Different Parts Of The Peripheral Vasculature, Including Renal Double Curve, Cobra, Multi – Purpose And Other Shapes ? Should Have Od Of 6F-8F Available ? Should Have The Largest Id For Each Od ? Should Have Lengths Ranging From 55-90 Cm , Transradial Guiding Catheter Right Curve/ Left Curve – Us Fda /Ce Approved ? Should Be Braided With Low Friction Inner Layer ? Should Have Atraumatic Soft Tip ? Should Be Available In Various Tip Shapes And Curves For Access To Different Parts Of The Peripheral Vasculature, Including Renal Double Curve, Cobra, Multi – Purpose And Other Shapes ? Should Have Od Of 6F-8F Available ? Should Have The Largest Id For Each Od ? Should Have Lengths Ranging From 55-90 Cm , Radial Guiding Catheter Ikari Curve -Dcgi Approved ?Should Be Braided With Low Friction Inner Layer ?Should Have Atraumatic Soft Tip ?Should Be Available In Various Tip Shapes And Curves For Access To Different Parts Of The Vasculature ?Should Have Od Of 6F-8F Available ?Should Have The Largest Id For Each Od ?Should Have Lengths Ranging From 90 Cm Or Above , Guiding Catheter For Peripheral Vascular Use – Us Fda Approved ?Should Be Available In Various Tip Shapes And Curves For Access To Different Parts Of The Coronary Vasculature, Including Judkins, Multi – Purpose And Other Shapes ?Should Have Od Of 5F-8F Available ?Should Have Lengths Ranging From 55-100 Cm , Guiding Catheter For Peripheral Vascular Use – Ce Approved ?Should Be Available In Various Tip Shapes And Curves For Access To Different Parts Of The Coronary Vasculature, Including Judkins, Multi – Purpose And Other Shapes ?Should Have Od Of 5F-8F Available ?Should Have Lengths Ranging From 55-100 Cm , Guiding Catheter For Peripheral Vascular Use – Dcgi Approved ?Should Be Available In Various Tip Shapes And Curves For Access To Different Parts Of The Coronary Vasculature, Including Judkins, Multi – Purpose And Other Shapes ?Should Have Od Of 5F-8F Available ?Should Have Lengths Ranging From 55-100 Cm , Guiding Catheter For Peripheral Vascular Use (5- 10F)– Dcgi Approved ?Should Be Available In Various Tip Shapes And Curves For Access To Different Parts Of The Coronary Vasculature, Including Judkins, Multi – Purpose And Other Shapes ?Should Have Od Of 5F-10F Available ?Should Have Lengths Ranging From 55-100 Cm , Long Sheath For Contra – Lateral Iliac/ Femoral Access – Us Fda Approved ?Should Be Low Friction With Inner Coating To Allow Catheter Manipulation ?Should Have Distal Radio-Opaque Tip For Enhanced Visibility On Fluoroscopy ?Should Have A Proximal Hemostasis Valve/ Provision For Tuohyborst Valve ?Shove Be Color Coded For Size Identification ?Should Be Available In 4F – 9 F Size With The Largest Id, Lengths Ranging From 40-110 Cm , Renal Guiding Catheter / Renal Guiding Catheter Double Curve/ Renal Guiding Catheter Single Curve – Us Fda /Ce Approved ?Should Be Braided With Low Friction Inner Layer Should Be Available In Various Tip Shapes And Curves For Access To Different Parts Of The Peripheral Vasculature, Including Renal Double Curve, Cobra, Multi – Purpose And Other Shapes ?Should Have Od Of 6F-8F Available, Should Have Lengths Ranging From 55-90 Cm , Renal Guiding Catheter / Renal Guiding Catheter Double Curve/ Renal Guiding Catheter Single Curve – Dcgi Approved ?Should Be Braided With Low Friction Inner Layer Should Be Available In Various Tip Shapes And Curves For Access To Different Parts Of The Peripheral Vasculature, Including Renal Double Curve, Cobra, Multi – Purpose And Other Shapes ?Should Have Od Of 6F-8F Available, Should Have Lengths Ranging From 55-90 Cm , Mother & Child Catheter – Us Fda/Ce Approved ?With Reliable Support With Large Inner Lumen And Inner Ptfe. , Mother & Child Catheter – Dcgiapproved ?With Reliable Support With Large Inner Lumen And Inner Ptfe. , Intubation Catheter For Assisting Delivery Of Stent In Difficult Anatomies – Us Fda/Ce Approved , Intubation Catheter For Assisting Delivery Of Stent In Difficult Anatomies – Dcgi Approved , Rdc Shape Guiding Catheter For Renal & C-Lilac Artery Angioplasty – - Us Fda/Ce / Dcgi Approved , Guide Extention Catheter: (Guide Plus Type) – Usfda/Pmda Approved Guide Extension Catheter Available In Variable Diameters Of 4.7F And 5.0F For Accessing Distal Anatomy And Delivering High Profile Devices; Guide Extension Catheter With A Tapered Distal Shaft For Accessing Distal And Challenging Coronary Anatomy; Guide Extension Catheter With A Resinous Atraumatic Tip; Guide Extension Catheter With A Large Entry Port Design For Easy Device Insertion , Guide Extention Catheter (Guidezilla Type) - Us Fda Approved ? 120 Proximal Hypo-Tube Shaft ? 0.57 Inner Diameter & 0.066” Outer Diameter ? Should Be With Proximal Marker And 1 X 1 Braiding , Guide Extention Catheter (Guidezilla Type) - Ce Approved ? 120 Proximal Hypo-Tube Shaft ? 0.57 Inner Diameter & 0.066” Outer Diameter ? Should Be With Proximal Marker And 1 X 1 Braiding , Guide Extention Catheter (Guidezilla Type) - Dcgi Approved ? 120 Proximal Hypo-Tube Shaft ? 0.57 Inner Diameter & 0.066” Outer Diameter Should Be With Proximal Marker And 1 X 1 Braiding , Manual Aspiration Catheter Aspiration Catheter Of 6F And 7F Guiding Catheter Compatibility; 140 Cm Working Length Catheter With 140 Cm Stylet Length; 90 Cm And 100 Cm Depth Markers; Provide 60Ml Aspiration Syringe For High Suction Efficiency; Large Size Collecting Filter. , Mechanical Aspiration Device – Usfda , Mechanical Aspiration Device – Ce/Dcgi , Thrombectomy Catheters With Distal Balloon Occlusion And Automated Suction During Ptca - Us Fda Approved , Thrombectomy Catheters With Distal Balloon Occlusion And Automated Suction During Ptca – Ce/Dcgi Approved , Thrombectomy Catheters With Motorized Cutting And Suction During Ptca - Us Fda Approved , Thrombectomy Catheters With Motorized Cutting And Suction During Ptca – Ce/Dcgi Approved , Aspiration Thrombectomy Catheter –1.30 Mm Square Suction Area - Usfda/Pmda Approved • Available In Size 6F, 7F Both, Must Have Entry Profile 0.019 Inches • Braided Polyamide Elastomer Shaft, Stainless Steel Wire Braiding And Guide Wire Type Stylet, • 6.0Mm Tip Length For Making Aspiration Inlet To Come Closer To The Target Thrombus And 10Cm-Length Depth. • Must Have Distal 40 Cm Hydrophilic Coating. , Aspiration Thrombectomy Catheter –1.30 Mm Square Suction Area – Ce Approved • Available In Size 6F, 7F Both, Must Have Entry Profile 0.019 Inches • Braided Polyamide Elastomer Shaft, Stainless Steel Wire Braiding And Guide Wire Type Stylet, • 6.0Mm Tip Length For Making Aspiration Inlet To Come Closer To The Target Thrombus And 10Cm-Length Depth. • Must Have Distal 40 Cm Hydrophilic Coating. , Aspiration Thrombectomy Catheter –1.30 Mm Square Suction Area – Dcgi Approved • Available In Size 6F, 7F Both, Must Have Entry Profile 0.019 Inches • Braided Polyamide Elastomer Shaft, Stainless Steel Wire Braiding And Guide Wire Type Stylet, • 6.0Mm Tip Length For Making Aspiration Inlet To Come Closer To The Target Thrombus And 10Cm-Length Depth. • Must Have Distal 40 Cm Hydrophilic Coating. , Computer Aided Vaccum Thrombectomy Catheter Kit Forvte Mechanical Aspiration With Working Length Of 100/115/130 Cm. ? Should Have Multi-Pitch, Laser-Cut Stainless Steel Hypotube For 1:1 Torque Transfer & Advance Deliverability. ? Catheter Should Have Id Of (3.33 Mm), Od Of 12 Fr With Htorq Tip With 50 Mm Circumferencial Sweep. ? Compatible With 12 Fr Sheath & Wire Platform (.014-.038) With Proprietoryseperator Technology. ? Aspiration Tubing Audio Visual Cues To Help Indicate Location Of Clot In System & Compatible With Engine With (-29.2) Inhg Deep Vacuum , Computer Aided Vaccum Thrombectomy Catheter Kit Forvte Mechanical Aspiration With Working Length Of 100 Cm With Flash Mode Designed For Expedited Venous Clot Removal. ? Should Have Multi-Pitch, Laser-Cut Stainless Steel Hypotube For 1:1 Torque Transfer & Advance Deliverability With Lightning Flash Tubing + Flash Catheter +Accessories + Select Catheter. ? Catheter Should Have Id Of 4.5 Mm, Od Of 16 Fr With Htorq Tip With 50 Mm Circumferencial Sweep. ? Compatible With 16 Fr Sheath & Wire Platform (.014-.038) With Proprietoryseperator Technology. ? Should Have Catheter Hub Port +Aspiration Tubing Port + Flow Cap + Flush Port As Rhv ? Packaged With 6F Select Catheter With Ber Or H1 Tip To Further Aid In Vessel Selection. ? Dual Clot Detection Algorithems With Max Id Technology. Aspiration Tubing Audio Visual Cues To Help Indicate Location Of Clot In System & Compatible With Engine With (-29.2) Inhg Deep Vacuum , Computer Aided Vaccum Thrombectomy Catheter Kit Forvte Mechanical Aspiration With Working Length Of 115 Cm With Flash Mode Designed For Expedited Venous Clot Removal. ? Should Have Multi-Pitch, Laser-Cut Stainless Steel Hypotube For 1:1 Torque Transfer & Advance Deliverability With Lightning Flash Tubing + Flash Catheter +Accessories + Select Catheter. ? Catheter Should Have Id Of (4.5 Mm), Od Of 16 Fr With Htorq Tip With 50 Mm Circumferencial Sweep. ? Compatible With 16 Fr Sheath & Wire Platform (.014-.038) With Proprietoryseperator Technology. ? Should Have Catheter Hub Port +Aspiration Tubing Port + Flow Cap + Flush Port As Rhv ? Packaged With 6F Select Catheter With Ber Or H1 Tip To Further Aid In Vessel Selection. ? Dual Clot Detection Algorithems With Max Id Technology. Aspiration Tubing Audio Visual Cues To Help Indicate Location Of Clot In System & Compatible With Engine With (-29.2) Inhg Deep Vaccum , Catheter- ? Stainless Steel Hypotube At The Proximal End,Designed To Enhance Deliverability To The Desired Vesselwith Optimal Visualization And Placement. ? Catheter Size : 6 F Catheter Type : Low Crossing Profile Of 1.75Mm With An Id Of .044”. ? Separator : Proprietary Separator Technology For Easy And Quick Aspiration, With 200 Cm Length And Distal Od Of .89 Mm. Safety Features : Ability To Get The Clot Out And Not Macerate . , Separator Componant: ? 150Cm - Proprietary Separator Technology For Easy And Quick Aspiration, With150 Cm Length And Distal Od Of 1.83 Mm. ? 175 Cm - Proprietary Separator Technology For Easy And Quick Aspiration, With175 Cm Length And Distal Od Of 1.40 Mm. , Aspiration Source - Engine Canister _ ? 1 Litre Capacity Collecting Jar With Measuring Marks. Integrated Clot Catcher With Completely Airtight And Break Resistant To – 2 Atm Pressure. Single Touch Operation. Led Canister Lighting. , Engine Powerful Aspiration Pump ? With 29-Inch Hg Deep Vacuum. Canister With Integrated Clot Catheter. Led Canister Should Be Sleek And Simple Design. , Coronary Micro-Guide Catheter With Gold Marker– Distal 70 Cm Hydrophilic Coat. Usfda/Pmda Approved • Must Have Tapered Stainless Steel Braid Mesh Construction And Inner Ptfe Layer. • Must Have 13 Cm Floppy Distal Segment, 70Cm Distal Hydrophilic Coating • Must Have Distal Outer Diameter 1.8 Fr Or Less And Proximal Outer Diameter 2.6Fr. • Catheter Length 130Cm For Antegrade Approach And 150 Cm For Retrograde Approach. , Coronary Micro-Guide Catheter With Gold Marker– Distal 70 Cm Hydrophilic Coat. Ce/Dcgi Approved • Must Have Tapered Stainless Steel Braid Mesh Construction And Inner Ptfe Layer. • Must Have 13 Cm Floppy Distal Segment, 70Cm Distal Hydrophilic Coating • Must Have Distal Outer Diameter 1.8 Fr Or Less And Proximal Outer Diameter 2.6Fr. • Catheter Length 130Cm For Antegrade Approach And 150 Cm For Retrograde Approach. , Re-Entry Catheter For Cto For Coronary – Us Fda/Ce / Dcgi Approved , Re-Entry Wire For Cto For Coronary – Us Fda/Ce / Dcgi Approved , Re-Entry Balloon With Two Exit Port For Cto For Coronary – Us Fda/Ce / Dcgi Approved , Microcatheter – Tip Entry – 1.3F - 135, 150 Cm - Usfda Approved • Tapered Soft Tip, Tip Entry 1.3 Fr Distal 2.6 Fr & Proximal 2.8 Fr Having Shinka Shaft Length 135 & 150 Cm • Usfda Approved , Microcatheter –Tip Entry – 1.3F -135, 150 Cm – Ce/Dcgi Approved • Tapered Soft Tip, Tip Entry 1.3 Fr Distal 2.6 Fr & Proximal 2.8 Fr Having Shinka Shaft Length 135 & 150 Cm • Usfda Approved , Microcatheter – Tip Entry – 1.4F -135, 150 Cm - Usfda Approved • Tapered Soft Tip, Tip Entry 1.4 Fr Distal 1.9 Fr & Proximal 2.6 Fr Having Shinka Shaft Length 135 & 150 Cm • Usfda Approved , Microcatheter – Tip Entry – 1.4F -135, 150 Cm – Ce/Dcgi Approved • Tapered Soft Tip, Tip Entry 1.4 Fr Distal 1.9 Fr & Proximal 2.6 Fr Having Shinka Shaft Length 135 & 150 Cm • Usfda Approved , Microcatheter - Double Lumen – Usfda Approved , Microcatheter - Double Lumen – Usfda Approved , Coaxial Microcatheter System For Peripheral Vessels – Usfda/Pmda Approved ? 2.8Fr And 2.4Fr - 2.4 And 2.0Fr Pre-Shaped Tip ? Tungsten Coil Pitch Construction, Ptfe Inner Layer, Dmso Compatible, Radiopaque 0.7 Mm Platinum/Iridium Markers , Coaxial Microcatheter System For Peripheral Vessels – Ce/Dcgi Approved ? 2.8Fr And 2.4Fr - 2.4 And 2.0Fr Pre-Shaped Tip Tungsten Coil Pitch Construction, Ptfe Inner Layer, Dmso Compatible, Radiopaque 0.7 Mm Platinum/Iridium Markers , Radial Artery Haemostasis Device- (Trans Radial Band) – Usfda/Pmda Approved ?Sizes – 24Cm And 29Cm, Must Have Belt Magic Tape For Fast Application. ?Consists Of Two Balloon Specially Designed For Spot Compression Of The Radial Puncture Site. ?Must Have Curved Support Plate. Must Have Green Positioning Marker , Radial Artery Haemostasis Device- (Trans Radial Band) – Ce/Dcgi Approved ?Sizes – 24Cm And 29Cm, Must Have Belt Magic Tape For Fast Application. ?Consists Of Two Balloon Specially Designed For Spot Compression Of The Radial Puncture Site. Must Have Curved Support Plate. Must Have Green Positioning Marker , Femoral Compression Devices – Disc / Dome Based Compression- Us Fda Approved , Femoral Compression Devices – Disc / Dome Based Compression – Ce/Dcgi Approved , Icd/Pi Compression Devices , Ptca/Coronary Angiography Drap Set ?Contains Absorbable Disposable Woven Cloth Sheet Of Size 1.5 Meter Z 2.5 Meter (2No) ?Contains Absorbable Disposable Woven Cloth Sheet Of Size 1.5 Meter X 1Metr (2No) , G- Kit Type Disposable Surgeons Gown Set , Disposable Plastic Sheet Of Size 1.5X2.5 Mtr , Angiography Cine Recordable Disk- Compact R Type Media With Cover With Govt. Medical College Kota & M.C Logo Printed Over The Cover , Angiography Cinerecordable -Digital Versetile – Rtype Media With Cover With Govt. Medical College Kota & M.C Logo Printed Over The Cover , G-Kit Type Disposable Sterile Surgeon Gowns , Disposable E.O. Sterile Angiography Drap Set Kit (Radial), ?Should Have Two Long Disposable Sheet In Both Sizes ?( 1.50 Meter X 1.0 Meter With Hole Of 3 Inch Radius -1 Quantity) ?( 1.50 Meter X 2.5 Meter With Hole Of 3 Inch Radius – 2 In Quantity) , Disposable E.O Sterile Angiography Drap Set Kit (Femoral), ?Should Have Two Long Disposable Sheet In Both Sizes ?( 1.50 Meter X 1.0 Meter With Hole Of 3 Inch Radius -1 Quantity), ?( 1.50 Meter X 2.5 Meter With Hole Of 3 Inch Radius – 2 In Quantity) , Long Disposable E.O Sterile Sheet(1.50 Meter X 2.5 Meter Size) , Small Disposable E.O Sterile Sheet(1.50 Meter X 1.0 Meter Size) , Rat Pad Type Radiation Protection Device Shield In All Sizes , Disposable Radiation Protection Shields & Drapes ? Disposable Non Fenestrated Lead Free Absorbable Sterile Barrier Pad For Protection During Fluoroscopy For Coronary Interventional Procedures With A Minimum Thickness Of 0.25 Mm Lead Equivalence, With Patented Bi-Layer Homogenous Sheet Tested & Certified To Iec 61-1:2014, Astm F3094-14, Din 6857-1, Usfda Approved, Iso 13485 & Barc Certified With Attenuation Greater Than 92% At 90Kvp. Dimensions: 12” X 17” , Disposable Radiation Protection Shields & Drapes ? Disposable Scoop Fenestrated Lead Free Absorbable Sterile Barrier Pad For Protection During Fluoroscopy For Coronary Interventional Procedures With A Minimum Thickness Of 0.25 Mm Lead Equivalence, With Patented Bi-Layer Homogenous Sheet Tested & Certified To Iec 61-1:2014, Astm F3094-14, Din 6857-1, Usfda Approved, Iso 13485 & Barc Certified With Attenuation Greater Than 92% At 90Kvp. Dimensions: 12” X 17”, Fenestration: 3.5” X 1.5” , Disposable Radiation Protection Shields & Drapes ? Disposable Circular Fenestrated Lead Free Absorbable Sterile Barrier Pad For Protection During Fluoroscopy For Coronary Interventional Procedures With A Minimum Thickness Of 0.25 Mm Lead Equivalence, With Patented Bi-Layer Homogenous Sheet Tested & Certified To Iec 61-1:2014, Astm F3094-14, Din 6857-1, Usfda Approved, Iso 13485 & Barc Certified With Attenuation Greater Than 92% At 90Kvp. Dimensions: 12” X 17”, Fenestration: Circle Fenestration: 1.5” , Disposable Radiation Protection Shields & Drapes ? Disposable Non Fenestrated Lead Free Absorbable Sterile Barrier Pad For Protection During Fluoroscopy For Peripheral Interventional Procedures With A Minimum Thickness Of 0.25 Mm Lead Equivalence, With A Minimum Length Of 34 Inches And Covering The Length From Hip To Toe; With Patented Bi-Layer Homogenous Sheet Tested & Certified To Iec 61-1:2014, Astm F3094-14, Din 6857-1, Usfda Approved, Iso 13485 & Barc Certified With Attenuation Greater Than 92% At 90Kvp. Dimensions: 12” X 34” , Disposable Radiation Protection Caps Disposable Non Fenestrated Lead-Free Absorbable Head Cap For Protection During Fluoroscopy For Interventional Procedures With A Minimum Thickness Of 0.25 Mm Lead Equivalence And Usfda Approved , External Temporary Pacemaker , Ptca Guide Wire – 2 Mm Silicon Coated Distal Tip, 0.014” Diameter And 180 Cm Length – Usfda/Pmda Approved • Must Have Platinum Coil At Distal Tip. Balance Of Hydrophilic And Hydrophobic Coating • Must Have Directly Jointed Sus And Nitinol Shaft Through Duocore Technology And Silicon Coated Joint. • Must Have Ptfe Coating From 25 To 180 Cm Length. & Mucus Coat Hydrophilic Coating Up To 248 Mm • Should Have 0.6 & 1.0 Gram Force Tip Loads , Ptca Guide Wire – 2 Mm Silicon Coated Distal Tip, 0.014” Diameter And 180 Cm Length – Ce/Dcgi Approved • Must Have Platinum Coil At Distal Tip. Balance Of Hydrophilic And Hydrophobic Coating • Must Have Directly Jointed Sus And Nitinol Shaft Through Duocore Technology And Silicon Coated Joint. • Must Have Ptfe Coating From 25 To 180 Cm Length. & Mucus Coat Hydrophilic Coating Up To 248 Mm • Should Have 0.6 & 1.0 Gram Force Tip Loads , Cto Stiff Ptca Wire - 3.6-Gram Force Tip Load – 2 Mm Silicon Coated Distal Tip, 0.014” Diameter And 180 Cm – Usfda/Pmda Approved •Must Have Platinum Coil At Distal Tip. Balance Of Hydrophilic And Hydrophobic Coating •Must Have Directly Jointed Sus And Nitinol Shaft Through Duocore Technology And Silicon Coated Joint. •Must Have M Coat Hydrophilic Coating Up To 248 Mm & Ptfe Coating From 25 To 180 Cm Length. ? Should Have 3.6-Gram Fore Tip Load , Cto Stiff Ptca Wire - 3.6-Gram Force Tip Load – 2 Mm Silicon Coated Distal Tip, 0.014” Diameter And 180 Cm – Ce/Dcgi Approved •Must Have Platinum Coil At Distal Tip. Balance Of Hydrophilic And Hydrophobic Coating •Must Have Directly Jointed Sus And Nitinol Shaft Through Duocore Technology And Silicon Coated Joint. •Must Have M Coat Hydrophilic Coating Up To 248 Mm & Ptfe Coating From 25 To 180 Cm Length. •Should Have 3.6-Gram Fore Tip Load , Ptca Guidewire For Septal Navigation - 0.03 Gm Tip Load– Usfda Approved •Tip Load 0.3 Gm, Hydrophilic Coating With Sion Tec Technology, Coil Length 19 Cm, Length 190 Cm & 300 Cm , Ptca Guidewire For Septal Navigation - 0.03 Gm Tip Load – Ce/Dcgi Approved •Tip Load 0.3 Gm, Hydrophilic Coating With Sion Tec Technology, Coil Length 19 Cm, Length 190 Cm & 300 Cm , Ptca Guidewire For Cto – 3 Gm Tip Load - 8.5 Cm Spring Coil - Usfda Approved •Stainless Core, Actone Technology, Polymer Jacket With Hydrophilic Coating, Tip Load 3 Gm, Radiopaque Length 3 Cm, Spring Coil 8.5 Cm, Length 190 Cm & 300 Cm , Ptca Guidewire For Cto – 3 Gm Tip Load - 8.5 Cm Spring Coil - Ce/Dcgi Approved •Stainless Core, Actone Technology, Polymer Jacket With Hydrophilic Coating, Tip Load 3 Gm, Radiopaque Length 3 Cm, Spring Coil 8.5 Cm, Length 190 Cm & 300 Cm , Ptca Guidewire For Cto – 3 Gm Tip Load – 3 Cm Spring Coil – Usfda Approved •Stainless Core, Actone Technology, Polymer Jacket With Hydrophilic Coating, Tip Load 3 Gm, Radiopaque Length 3 Cm, Spring Coil 3 Cm, Length 190 Cm & 300 Cm , Ptca Guidewire For Cto – 3 Gm Tip Load – 3 Cm Spring Coil – Ce/Dcgi Approved •Stainless Core, Actone Technology, Polymer Jacket With Hydrophilic Coating, Tip Load 3 Gm, Radiopaque Length 3 Cm, Spring Coil 3 Cm, Length 190 Cm & 300 Cm , Ptca Guidewire For Cto – 3 Gm Tip Load – 11 Cm Spring Coil – Usfda Approved •Stainless Core, Actone Technology, Polymer Jacket Length 40 Cm With Hydrophilic Coating 50 Cm, Tip Load 3 Gm, Radiopaque Length 3 Cm, Spring Coil 11 Cm, Length 200 Cm & 300 Cm With Straight Tip & 1 Mm Pre Shape , Ptca Guidewire For Cto – 3 Gm Tip Load – 11 Cm Spring Coil – Ce/Dcgi Approved •Stainless Core, Actone Technology, Polymer Jacket Length 40 Cm With Hydrophilic Coating 50 Cm, Tip Load 3 Gm, Radiopaque Length 3 Cm, Spring Coil 11 Cm, Length 200 Cm & 300 Cm With Straight Tip & 1 Mm Pre Shape , Ptca Guidewire For Cto – 0.6 Gm Tip Load – 28 Cm Spring Coil – Usfda Approved Sion Tecc Technology, Actone Braiding, 17 Cm Polymer Jacket 17 Cm Slip Coat Coating, Radiopaque Length 16 Cm 28 Cm Spring Coil, Tapered Tip 0.010-Inch, Tip Load 0.6 Gm , Ptca Guidewire For Cto – 0.6 Gm Tip Load – 28 Cm Spring Coil – Ce/Dcgi Approved Sion Tecc Technology, Actone Braiding, 17 Cm Polymer Jacket 17 Cm Slip Coat Coating, Radiopaque Length 16 Cm 28 Cm Spring Coil, Tapered Tip 0.010-Inch, Tip Load 0.6 Gm , Ptca Guidewire For Cto – 1.0 Gm Tip Load – 28 Cm Spring Coil – Usfda Approved Sion Tecc Technology, Actone Braiding, 17 Cm Polymer Jacket 17 Cm Slip Coat Coating, Radiopaque Length 16 Cm 28 Cm Spring Coil, Tapered Tip 0.010-Inch, Tip Load 1.0 Gm , Ptca Guidewire For Cto – 1.0 Gm Tip Load – 28 Cm Spring Coil – Ce/Dcgi Approved Sion Tecc Technology, Actone Braiding, 17 Cm Polymer Jacket 17 Cm Slip Coat Coating, Radiopaque Length 16 Cm 28 Cm Spring Coil, Tapered Tip 0.010-Inch, Tip Load 1.0 Gm , Ptca Guidewire For Cto – 1.7, 3.5, 4.5 Gm Tip Load – 15 Cm Spring Coil – Usfda Approved ? Sion Tecc Technology, Actone Braiding, Spring Coil Length 15 Cm, Radiopaque Length 15 Cm, Tapered Tip 0.010 Inch ? Gaia 1St Tip Load 1.7 Gm Tapered Tip 0.011 Inch ? Gaia 2Nd Tip Load 3.5 Gm, Tapered Tip 0.012 Inch ? Gaia 3Rd Tip Load 4.5 Gm, •All Are Mini - Pre Shaped 1Mm 45 Degree Angle , Micro Cone Tip Used For Cto Cases , Ptca Guidewire For Cto – 1.7, 3.5, 4.5 Gm Tip Load – 15 Cm Spring Coil – Ce/Dcgi Approved ? Sion Tecc Technology, Actone Braiding, Spring Coil Length 15 Cm, Radiopaque Length 15 Cm, Tapered Tip 0.010 Inch ? Gaia 1St Tip Load 1.7 Gm Tapered Tip 0.011 Inch ? Gaia 2Nd Tip Load 3.5 Gm, Tapered Tip 0.012 Inch ? Gaia 3Rd Tip Load 4.5 Gm, ? All Are Mini - Pre Shaped 1Mm 45 Degree Angle , Micro Cone Tip Used For Cto Cases , Ptca Guidewire For Cto – 3.0 Gm Tip Load ? Single Core , Core To Tip , Tip Load 3 Gm , Tip Radiopacity 3 Cm , Tip Diameter 0.014 Inch , Tip Radiopacity 11 Cm , Slip Coat Over The Spring Coil Used For Cto Lesion , Ptca Guidewire For Cto – 3.0, 6.0, 12 Gm Tip Load ? Single Core , Core To Tip , Tip Load 3 Gm ,6 Gm , 12 Gm Tip Radiopacity 3 Cm , Tip Diameter 0.014 Inch , Tip Radiopacity 11 Cm , Silicone Coating Coat Over The Spring Coil Used For Cto Lesion , Ptca Guidewire For Cto – 9.0, 12, 20 Gm Tip Load ? Single Core Core To Tip , Tip Load 9 Gm Tapered 0.090 , 12 Gm Tapered 0.090 Inch & 20 Gm Tapered Tip 0.080 Inch For Cto Lesion , Ptca Guidewire For Cto – 3.0 Gm Tip Load Single Core Core To Tip , Tip Load 3 Gm, Radiopacity 3 Cm , Guide Wire Length 330 Cm , Slip Coat Over The Spring Coil , Ptca Guidewire For Cto – 2.0, 4.0, 6.0 Gm Tip Load ? Sion Tecc Technology, Actone Braiding, Spring Coil Length 15 Cm , Radiopaque Length 15 Cm , Tapered Tip 0.010 Inch ? Gaia 1St Tip Load 2 Gm Tapered Tip 0.011 Inch ? Gaia 2Nd Tip Load 4 Gm, Tapered Tip 0.012 Inch ? Gaia 3Rd Tip Load 6 Gm, ? All Are Mini - Pre Shaped 1Mm 45 Degree Angle , Micro Cone Tip , Xtrand Coil , Ptca Wires With Facility Of Boot Links For Extension Of Regular Wire - Us Fda Approved , Micro-Wire (0.008”-0.012” ) With Hydrophilic Coating , Special Inflation Device For High Pressure (55 Atm), High Resolution , Ptca Wire – Tip Load - 0.5-0.7Gm – Usfda Approved ? Regular Workhorse Guidewire With Tapered Elastinite Nitinol Core, Durasteel Ribbon Tip And Available In Both Hydrophilic And Hydrophobic Coatings Between Tip Load 0.5-0.7Gm , Ptca Wire – Tip Load - 0.5-0.7Gm –With Intermediate Polymer Sleeve - Usfda Approved ? Regular Workhorse Guidewire With Elastinite Nitinol Core, Hyten Stainless Steel Tip, Intermediate Polymer Sleeve With Hydrocoat On Distal Tip Between Tip Load 0.5-0.7Gm , Ptca Wire – Tip Load - 0.5-0.7Gm –With Intermediate Polymer Sleeve - Ce/Dcgi Approved ? Regular Workhorse Guidewire With Elastinite Nitinol Core, Hyten Stainless Steel Tip, Intermediate Polymer Sleeve With Hydrocoat On Distal Tip Between Tip Load 0.5-0.7Gm , Ptca Wire – Tip Load - 0.5-0.7Gm –With Hyten Stainless Steel Tip - Usfda Approved ? Regular Workhorse Guidewire With Elastinite Nitinol Core, Hyten Stainless Steel Tip Intermediate Polymer Sleeve With Smoothglide Coating On Proximal And Turbocoat On Distal Tip Between Tip Load 0.5-0.7Gm , Ptca Wire – Tip Load - 0.5-0.7Gm –With Hyten Stainless Steel Tip - Ce/Dcgi Approved ? Regular Workhorse Guidewire With Elastinite Nitinol Core, Hyten Stainless Steel Tip Intermediate Polymer Sleeve With Smoothglide Coating On Proximal And Turbocoat On Distal Tip Between Tip Load 0.5-0.7Gm , Ptca Wire – Tip Load – 0.6 Gm –With Stainless Steel Core With Shaping Ribbon Tip - Usfda Approved ? Regular Workhorse Guidewire With Tapered Stainless Steel Core And Shaping Ribbon Tip Available In Tip Load Of 0.6Gm With Poly Tetra Fluoro Ethylene Coating On Proximal End , Ptca Wire – Tip Load – 0.6 Gm –With Stainless Steel Core With Shaping Ribbon Tip – Ce/Dcgi Approved ? Regular Workhorse Guidewire With Tapered Stainless Steel Core And Shaping Ribbon Tip Available In Tip Load Of 0.6Gm With Poly Tetra Fluoro Ethylene Coating On Proximal End , Ptca Wire – Tip Load – 0.8 Gm – Responsease Core Grind With Palladium-Rhenium Tip – Usfda Approved ? Regular Workhorse Guidewire With Responsease Core Grind Technology And 3Cm Palladium-Rhenium Radiopaque Distal Tip Available In Tip Load Of 0.8Gm With 190 And 300Cm , Ptca Wire – Tip Load – 0.8 Gm – Responsease Core Grind With Palladium-Rhenium Tip – Ce/Dcgi Approved ? Regular Workhorse Guidewire With Responsease Core Grind Technology And 3Cm Palladium-Rhenium Radiopaque Distal Tip Available In Tip Load Of 0.8Gm With 190 And 300Cm , Ptca Wire – Tip Load – 0.9 Gm – Responsease Core Grind With Uncoated Tip – Usfda Approved ? Workhorse Guidewire With Durasteel Core, Responsease Core Grind Technology And 1.5 Cm Uncoated Distal Tip For Tactile Feedback Available In Multiple Variants With Exact Same Tip Load Of 0.9Gm , Ptca Wire – Tip Load – 0.9 Gm – Responsease Core Grind With Uncoated Tip – Ce/Dcgi Approved ? Workhorse Guidewire With Durasteel Core, Responsease Core Grind Technology And 1.5 Cm Uncoated Distal Tip For Tactile Feedback Available In Multiple Variants With Exact Same Tip Load Of 0.9Gm , Ptca Wire – Tip Load – 0.6-.8 Gm – Triple Spring With Rotary Swagging Tip – Usfda Approved ? Workhorse Guidewire With Triple Spring 304V Stainless Steel With Niti Distal Core And Cold Working Rotary Swagging Tip Available In Tip Loads Between 0.6-0.8Gm And Lengths (190/300Cm). , Ptca Wire – Tip Load – 0.6-.8 Gm – Triple Spring With Rotary Swagging Tip – Ce/Dcgi Approved ? Workhorse Guidewire With Triple Spring 304V Stainless Steel With Niti Distal Core And Cold Working Rotary Swagging Tip Available In Tip Loads Between 0.6-0.8Gm And Lengths (190/300Cm). , Speciality Ptca Wire – Low Support - Tip Load 0.8-1.0 Gm – Usfda Approved ? Low Support Durasteel Guidewire With Full Polymer Coating Available In Tip Loads Between 0.8-1.0Gm , Speciality Ptca Wire – Low Support - Tip Load 0.8-1.0 Gm – Ce/Dcgi Approved ? Low Support Durasteel Guidewire With Full Polymer Coating Available In Tip Loads Between 0.8-1.0Gm , Speciality Ptca Wire – Medium Support - Tip Load 1.0-1.2 Gm – Usfda Approved ? Medium Support Durasteel Guidewire With Full Polymer Coating Available In Tiploads Between 1.0-1.2Gm , Speciality Ptca Wire – Medium Support - Tip Load 1.0-1.2 Gm – Ce/Dcgi Approved ? Medium Support Durasteel Guidewire With Full Polymer Coating Available In Tiploads Between 1.0-1.2Gm , Speciality Ptca Wire – Extra Support - Tip Load 1.0-1.2 Gm – Usfda Approved ? Extra Support Durasteel Guidewire With Full Polymer Coating Available In Tiploads Between 1.0-1.2Gm , Speciality Ptca Wire – Extra Support - Tip Load 1.0-1.2 Gm – Ce/Dcgi Approved ? Extra Support Durasteel Guidewire With Full Polymer Coating Available In Tiploads Between 1.0-1.2Gm , Speciality Ptca Wire – Extra Support - Tip Load 1.3-1.5 Gm – Usfda Approved ? Extra Support Durasteel Guidewire With Full Polymer Cover, Marker At 4.5Cm From Distal Tip And Tipload Between 1.3-1.5Gm , Speciality Ptca Wire – Extra Support - Tip Load 1.3-1.5 Gm – Ce/Dcgi Approved ? Extra Support Durasteel Guidewire With Full Polymer Cover, Marker At 4.5Cm From Distal Tip And Tipload Between 1.3-1.5Gm , Speciality Ptca Wire – Stainless Steel - Tip Load 1.0 Gm – Usfda Approved ? Stainless Steel Guidewire With Stainless Steel Coils And Hydrophilic Coating Availabe In Tipload Of 1Gm With Radioapaque Tip Of 3Cm , Speciality Ptca Wire – Stainless Steel - Tip Load 1.0 Gm – Ce/Dcgi Approved ? Stainless Steel Guidewire With Stainless Steel Coils And Hydrophilic Coating Availabe In Tipload Of 1Gm With Radioapaque Tip Of 3Cm , Speciality Ptca Wire – Stainless Steel - Tip Load 0.6 - 0.7 Gm – Usfda Approved ? Stainless Steel Guidewire With Intermediate Polymer Sleeve And Hydrophobic Coating Availabe In Tipload Between 0.6-0.7Gm With Radioapaque Tip Of 3Cm , Speciality Ptca Wire – Stainless Steel - Tip Load 0.6 - 0.7 Gm – Ce/Dcgi Approved ? Stainless Steel Guidewire With Intermediate Polymer Sleeve And Hydrophobic Coating Availabe In Tipload Between 0.6-0.7Gm With Radioapaque Tip Of 3Cm , Speciality Ptca Wire – Elastinite Nitinol - Tip Load 0.7 - 0.8 Gm – Usfda Approved ? Elastinite Nitinol Guidewire With Shaping Ribbon Tip And Hydrophilic Coating Avaialble In Tipload Between 0.7-0.8Gm With Radiopaque Tip Of 4.5Cm , Speciality Ptca Wire – Elastinite Nitinol - Tip Load 0.7 - 0.8 Gm – Ce/Dcgi Approved ? Elastinite Nitinol Guidewire With Shaping Ribbon Tip And Hydrophilic Coating Avaialble In Tipload Between 0.7-0.8Gm With Radiopaque Tip Of 4.5Cm , Speciality Ptca Wire – Stainless Steel - Tip Load 1.7, 4.7, 6.2, 8.7 Gm – Usfda Approved ? Stainless Steel Penetration Guidewire With Core-To-Tip Design And Hydrophilic Coating Available In Tipload Of 1.7, 4.7, 6.2, 8.7 Gm , Speciality Ptca Wire – Stainless Steel - Tip Load 1.7, 4.7, 6.2, 8.7 Gm – Ce/Dcgi Approved ? Stainless Steel Penetration Guidewire With Core-To-Tip Design And Hydrophilic Coating Available In Tipload Of 1.7, 4.7, 6.2, 8.7 Gm , Speciality Ptca Wire – Durasteel - Tip Load 2.5-2.7 Gm – Usfda Approved ? Extra Support Durasteel Cto Guidewire With Full Polymer Cover, Gold Marker At 4.5Cm From Distal Tip And Tipload Between 2.5-2.7Gm , Speciality Ptca Wire – Durasteel - Tip Load 2.5-2.7 Gm – Ce/Dcgi Approved ? Extra Support Durasteel Cto Guidewire With Full Polymer Cover, Gold Marker At 4.5Cm From Distal Tip And Tipload Between 2.5-2.7Gm , Ptca Wire For Cto Tip Load –4.5-4.8 – Usfda Approved ? Cto Guidewire Having Durasteel Core, Intermediate Polymer Sleeve Available In Tipload Between 4.5-4.8Gm Tipload And Penetration Power Of 40 Kgpsin , Ptca Wire For Cto Tip Load –9.5-9.7– Usfda Approved ? Ptca Cto Guidewire Having Durasteel Core, Intermediate Polymer Sleeve Available In Tipload Between 9.5-9.7Gm Tipload And Penetration Power Of 80 Kgpsin , Ptca Wire For Cto Tip Load –13.5-13.9 – Usfda Approved ? Ptca Cto Guidewire Having Durasteel Core, Intermediate Polymer Sleeve Available In Tipload Between 13.5-13.9Gm Tipload And Penetration Power Of 120 Kgpsin , Ptca Wire For Cto Tip Load –12-12.5 – Usfda Approved Cto Guidewire Having Durasteel Core, Intermediate Polymer Sleeve Available In Tipload Between 12.0-12.5Gm Tipload And Penetration Power Of 140 Kgpsin , Ptca Wire For Cto Tip Load –12.8-13.0 – Usfda Approved Cto Guidewire Having Durasteel Core, Intermediate Polymer Sleeve Available In Tipload Between 12.8-13.0Gm Tipload And Penetration Power Of 200 Kgpsin , Ptca Wire For Cto – Tip Load – 11, 14 Gm - Usfda Approved Cto Guidewire Having Having Durasteel Core, Hydrophilic Coating (Excluding The Tip) For Lubricity And Ease Of Movement Within A Microcathete, Textured Tip With Tip Size Of 0.009 Inches And Tip Angle Of 25 Degrees At 1 Mm Of Tip. Should Have The Tip Load Of 11, 14Gm , High Pressure Non-Compliant Balloon – Three Pleats Re-Wrappable Structure - Pmda Approved •With Innovative Triple Layer Balloon Technology With High Pressure Resistance Of 22 Atm. •Must Have Elastomer Outer Layer, Middle Layer Of Polyamide And Inner Most Layer Of Elastomer. •Must Have Nominal Pressure Of 12Atm And Rbp Of 22Atm. •Shorter Thin Distal Tip Of 2.9Mm With Low Entry Profile Of 0.43 Mm. Must Have Hydrophilic Mucus Coating •Must Have 3.0 Mm Short Taper Balloon Shoulder & Must Have 0.8Mm Shorter And 25?M Thinner Radiopaque Marker For Lower Crossing Profile. •Must Have 2.6 French Stainless Steel Core Wire Structured Shaft & Stainless-Steel Stylet In Mid Shaft. Must Have Hypotube Without Ptfe Coating. , High Pressure Non-Compliant Balloon – Three Pleats Re-Wrappable Structure – Ce/Dcgiapproved ? With Innovative Triple Layer Balloon Technology With High Pressure Resistance Of 22 Atm. ? Must Have Elastomer Outer Layer, Middle Layer Of Polyamide And Inner Most Layer Of Elastomer. ? Must Have Nominal Pressure Of 12Atm And Rbp Of 22Atm. ? Shorter Thin Distal Tip Of 2.9Mm With Low Entry Profile Of 0.43 Mm. Must Have Hydrophilic Mucus Coating ? Must Have 3.0 Mm Short Taper Balloon Shoulder & Must Have 0.8Mm Shorter And 25?M Thinner Radiopaque Marker For Lower Crossing Profile. ? Must Have 2.6 French Stainless Steel Core Wire Structured Shaft & Stainless-Steel Stylet In Mid Shaft. Must Have Hypotube Without Ptfe Coating. , Cto Balloon With Ultra – Ultra Low Entry Profile Of 0.016 Must Have Hydrophilic Mucus Coating -Pmda Approved ? Should Have Smallest Diameter 1.00Mm And 5Mm Length. - Three Pleats Re-Wrappable Structure. ? Must Have 0.8Mm Shorter And 25?M Thinner Radiopaque Marker For Lower Crossing Profile. ? Must Have Flexible Tip With Short Balloon Bonding Part Of 0.4Mm. ? Nominal Pressure Of 06 Atm And Rbp Of 14 Atm ? Must Have 2.4 To 2.7 French Tapered Stainless Steel Core Wire Structured Shaft , Cto Balloon With Ultra – Ultra Low Entry Profile Of 0.016 Must Have Hydrophilic Mucus Coating -Ce/Dcgi Approved ? Should Have Smallest Diameter 1.00Mm And 5Mm Length. - Three Pleats Re-Wrappable Structure. ? Must Have 0.8Mm Shorter And 25?M Thinner Radiopaque Marker For Lower Crossing Profile. ? Must Have Flexible Tip With Short Balloon Bonding Part Of 0.4Mm. ? Nominal Pressure Of 06 Atm And Rbp Of 14 Atm ? Must Have 2.4 To 2.7 French Tapered Stainless Steel Core Wire Structured Shaft , Ptca Balloon Semi Compliant For Cto – Usfda Approved ? Cto Indicated Slim Seal Technology On Distal Tip With Lesion Entry Profile Of 0.016, Crossing Profile Of 0.021 And Single Flexible Tungsten Marker Available In Unique Diameter Of 1.2Mm With Variety Of Lengths ? Diameter – 1.2, 1.5. 2.0 ? Length – 6, 8, 12, 15, 20 & In 2Mm-25, 30 , Ptca Balloon Semi Compliant For Cto – Ce/Dcgi Approved ? Cto Indicated Slim Seal Technology On Distal Tip With Lesion Entry Profile Of 0.016, Crossing Profile Of 0.021 And Single Flexible Tungsten Marker Available In Unique Diameter Of 1.2Mm With Variety Of Lengths ? Diameter – 1.2, 1.5. 2.0 ? Length – 6, 8, 12, 15, 20 & In 2Mm-25, 30 , Ptca Balloon Semi Compliant – Usfda Approved ? With Slim Seal Technology On Distal Tip With Crossing Profile Of 0.021”, Lesion Entry Profile Of 0.017” And Microglide Coating Available In Diameter 2.25-5.00Mm And Lengths 6-30Mm ? Diameter – 2.25, 2.5, 2.75, 3.0, 3.25, 3.5, 3.75, 4.0, 4.5, 5.0 Mm ? Length - 6, 8, 12, 15, 20, 25, 30 , Ptca Balloon Semi Compliant – Ce/Dcgi Approved ? With Slim Seal Technology On Distal Tip With Crossing Profile Of 0.021”, Lesion Entry Profile Of 0.017” And Microglide Coating Available In Diameter 2.25-5.00Mm And Lengths 6-30Mm ? Diameter – 2.25, 2.5, 2.75, 3.0, 3.25, 3.5, 3.75, 4.0, 4.5, 5.0 Mm ? Length - 6, 8, 12, 15, 20, 25, 30 , Ptca Balloon Non-Compliant – Usfda Approved ? With Multilayer Crossflex Balloon Technology And Round Tip With Lesion Entry Profile Of 0.018” Available In Diameter 1.5Mm-5Mm And Lengths In 6Mm-25Mm With Skive Technology On Mid Shaft Of Dilatation Catheter ? Diameter – 1.5, 2.0, 2.25, 2.5, 2.75, 3.0, 3.25, 3.5, 3.75, 4.0, 4.5, 5.0 Mm ? Length- 6, 8, 12, 15, 20, 25 , Ptca Balloon Non-Compliant – Ce/Dcgi Approved ? With Multilayer Crossflex Balloon Technology And Round Tip With Lesion Entry Profile Of 0.018” Available In Diameter 1.5Mm-5Mm And Lengths In 6Mm-25Mm With Skive Technology On Mid Shaft Of Dilatation Catheter ? Diameter – 1.5, 2.0, 2.25, 2.5, 2.75, 3.0, 3.25, 3.5, 3.75, 4.0, 4.5, 5.0 Mm ? Length- 6, 8, 12, 15, 20, 25 , Ptca Balloon Non-Compliant – Usfda Approved ? Multilayer And Single Piece Outer Member And Large Hypotube And Visible Hub Printing Should Have Shorter Deflation Time And Shall Come In Sizes Of 1.5 Mm To 6 Mm ? Diameter – 1.5, 2.0, 2.25, 2.5, 2.75, 3.0, 3.25, 3.5, 3.75, 4.0, 4.5, 5.0, 5.5, 6.0 Mm ? Length- 6, 8, 12, 15, 20, 25 , Ptca Balloon Non-Compliant – Ce/Dcgi Approved ? Multilayer And Single Piece Outer Member And Large Hypotube And Visible Hub Printing Should Have Shorter Deflation Time And Shall Come In Sizes Of 1.5 Mm To 6 Mm ? Diameter – 1.5, 2.0, 2.25, 2.5, 2.75, 3.0, 3.25, 3.5, 3.75, 4.0, 4.5, 5.0, 5.5, 6.0 Mm ? Length- 6, 8, 12, 15, 20, 25 , Ptca Balloon Semi-Compliant – Ce Approved ? Balloon With Laser Bond Technology On Distal Tip With Crossing Profile Of 0.021” And Tip Entry Profile Of 0.017” Available In Diameter 2.25-5.00Mm And Lengths 6-30Mm ? Diameter –2.25, 2.5, 2.75, 3.0, 3.25, 3.5, 3.75, 4.0, 4.5, 5.0 Mm ? Length- 6, 8, 12, 15, 20, 25, 30 , Ptca Balloon Semi-Compliant –Dcgi Approved ? Balloon With Laser Bond Technology On Distal Tip With Crossing Profile Of 0.021” And Tip Entry Profile Of 0.017” Available In Diameter 2.25-5.00Mm And Lengths 6-30Mm ? Diameter –2.25, 2.5, 2.75, 3.0, 3.25, 3.5, 3.75, 4.0, 4.5, 5.0 Mm ? Length - 6, 8, 12, 15, 20, 25, 30 , Ptca Balloon Non-Compliant – Ce Approved ? Non-Complaint Coronary Balloon With Tri-Fold Layers And Tip Entry Profile Of 0.018” Available In Diameter 2.0-4.5Mm And Lengths In 8Mm-25Mm ? Diameter –2.0, 2.25, 2.5, 2.75, 3.0, 3.25, 3.5, 3.75, 4.0, 4.5 Mm ? Length - 8, 12, 15, 20, 25 Mm , Ptca Balloon Non-Compliant – Dcgi Approved ? Non-Complaint Coronary Balloon With Tri-Fold Layers And Tip Entry Profile Of 0.018” Available In Diameter 2.0-4.5Mm And Lengths In 8Mm-25Mm ? Diameter –2.0, 2.25, 2.5, 2.75, 3.0, 3.25, 3.5, 3.75, 4.0, 4.5 Mm ? Length - 8, 12, 15, 20, 25 Mm , Slender Profile Tapered Tip Cto Balloon Semi Compliant – With Unique Diameter 1Mm & 6Mm Length – Ce Approved ? Tapered Fit Tungsten Tip With Lesion Entry Profile Of 0.0158, With Tip Entry Id - .0145”Crossing Profile Of 0.021 ? Must Have Special Trifold Rewrap Design, With Selective Hydrophilic Coating Over Balloon ? Must Have Flexible Platinum Iridium Marker With Tungsten Tip ? Diameter – 1, 1.25, 1.5, 2.0, 2.25, 2.5, 2.75, 3.0, 3.25, 3.5, 3.75, 4.0, 4.5, 5.0 Mm, ? Length – 6, 9, 12, 15, 20, 30 Mm ? Must Have Nominal Pressure 8 Atm, Rbp -12 Atm , Tapered Tip Non-Compliant Ptca Balloon With Selective Hydrophilic Coating – Ce Approved ? Must Have Tapered Tungsten Tip With Tungsten Lesion Entry Profile Of 0.0158, With Tip Entry Id - .0145” Crossing Profile Of 0.021, Must Have Gradient Stiff Shaft ? Must Have Flexible Platinum Iridium Marker With Tungsten Tip ? Must Have Special Trifold Rewrap Design, With Selective Hydrophilic Coating Over Balloon ? Diameter –2.0, 2.25, 2.5, 2.75, 3.0, 3.25, 3.5, 3.75, 4.0, 4.5, 5.0 Mm, ? Length – 6, 8, 12, 15, 20, 30 Mm ? Must Have Nominal Pressure 12 Atm, Rbp -20 Atm , Spherical Tip Non-Compliant Lolipop Ptca Balloon With Selective Hydrophilic Coating – Ce Approved ? Must Have Spherical Tungsten Tip With Tungsten Lesion Entry Profile Of 0.0158, With Tip Entry Id - .0145”Crossing Profile Of 0.021, Must Have Gradient Stiff Shaft ? Must Have Flexible Platinum Iridium Marker With Tungsten Tip ? Must Have Special Trifold Rewrap Design, With Selective Hydrophilic Coating Over Balloon ? Diameter –2.0, 2.25, 2.5, 2.75, 3.0, 3.25, 3.5, 3.75, 4.0, 4.5, 5.0 Mm, ? Length – 6, 8, 12, 15, 20, 30 Mm ? Must Have Nominal Pressure 12 Atm, Rbp -20 Atm , Non-Compliant Ptca Balloon – Usfda Approved ? 0.017” Lesion Entry Profile, Crossing Profile - .031, Bi-Segmen Inner Shaft Design With Hydrophilic Coating, Over-The-Inner Tip Design, Slop Outer Shaft ? Platinum Iridium Marker Bands, Nominal Pressure 12 Atm, Rbp -18 Atm ? Diameter –2.0, 2.25, 2.5, 2.75, 3.0, 3.25, 3.5, 3.75, 4.0, 4.5, 5.0, 5.5, 6.0 Mm, ? Length – 6, 8, 12, 15, 20, 30 Mm , Non-Compliant Ptca Balloon – Ce/Dcgi Approved ? 0.017” Lesion Entry Profile, Crossing Profile - .031, Bi-Segmen Inner Shaft Design With Hydrophilic Coating, Over-The-Inner Tip Design, Slop Outer Shaft ? Platinum Iridium Marker Bands, Nominal Pressure 12 Atm, Rbp -18 Atm ? Diameter –2.0, 2.25, 2.5, 2.75, 3.0, 3.25, 3.5, 3.75, 4.0, 4.5, 5.0, 5.5, 6.0 Mm, ? Length – 6, 8, 12, 15, 20, 30 Mm , Semi-Compliant Ptca Balloon – Usfda Approved ? 0.017” Lesion Entry Profile, Crossing Profile - .026, Bi-Segmen Inner Shaft Design With Hydrophilic Coating, Unique, Over-The- Inner Tip Design: Outer Tip Material Rides Over The Inner Shaft Material, Slop Outer Shaft, Optileap Material Withzglide Hydrophilic Coating ? Platinum Iridium Marker Bands, Nominal Pressure 12 Atm, Rbp -18 Atm ? Diameter –1.2, 1.5, 2.0, 2.25, 2.5, 2.75, 3.0, 3.25, 3.5, 3.75, 4.0, 4.5, 5.0 Mm, ? Length – 8, 12, 15, 20, 30, 40 Mm , Semi-Compliant Ptca Balloon – Ce/Dcgi Approved ? 0.017” Lesion Entry Profile, Crossing Profile - .026, Bi-Segmen Inner Shaft Design With Hydrophilic Coating, Unique, Over-The- Inner Tip Design: Outer Tip Material Rides Over The Inner Shaft Material, Slop Outer Shaft, Optileap Material Withzglide Hydrophilic Coating ? Platinum Iridium Marker Bands, Nominal Pressure 12 Atm, Rbp -18 Atm ? Diameter –1.2, 1.5, 2.0, 2.25, 2.5, 2.75, 3.0, 3.25, 3.5, 3.75, 4.0, 4.5, 5.0 Mm, ? Length – 8, 12, 15, 20, 30, 40 Mm , 6F Kbt - Ultra Low Profile Semi Complaint Ptca Balloon – Multilayer Polyamide Sandwich - Ce Approved •Kbt Shaft Compliance - Proximal - 1.73 F, Distal : 2.67 F •Ultra-Low Tip Entry Profile -.040Mm - Crossing Profile: 0.72 Mm/0.028, Rewrap Profile Of 1.84 Mm •Soft Multi-Layered Polyamide Sandwich Design, Trifold Rewrap Design With Selective Hydrophilic Coating At Distal Shaft Including Balloon Tip, Nominal Pressure: 6 Atm, Rated Burst Pressure (Rbp) - 16 Atm (14 Atm For 4.5Mm) •Length (Mm): 9,12,15,20,25,30 ? Diameter(Mm): 2,2.25,2.50,2.75,3.00,3.25,3.5,3.75,4.00 & 4.5 Mm , 6F Kbt – Non-Complaint Ptca Balloon – Multilayer Polyamide Sandwich - Ce Approved ? Kbt Shaft Compliance - Proximal 1.95F, Distal 2.67F ? Ultra-Low Tip Entry Profile -.041Mm - Crossing Profile: 0.72 Mm/0.028, Rewrap Profile Of 1.84 Mm ? Soft Multi-Layered Polyamide Sandwich Design, Trifold Rewrap Design With Selective Hydrophilic Coating At Distal Shaft Including Balloon Tip, Nominal Pressure: 12 Atm, Rated Burst Pressure (Rbp) - 20 Atm. ? Shortest Shoulder Length Of 2.51 Mm ? Length (Mm): 6, 8, 10,12,15,20,25,30 ? Diameter(Mm): 2, 2.25, 2.50, 2.75, 3.00, 3.25, 3.5, 3.75, 4.00 & 4.5 Mm , Thinnest Wall 0.08 Semi Compliant Balloon – Long Length– Ce Approved ? Np -6 Atm, Rbp – 18 Atm, Crossing Profile .65 ? Diameter – 1.25, 1.5, 2.0, 2.25, 2.50, 2.75, 3.00, 3.25, 3.5, 4.00 & 4.5 Mm ? Length –10,12,15,20,25,30, 35, 40 , Angled Shoulder Non-Compliant Balloon – Long Length– Ce Approved ? Angled Shoulder Balloon With Trifold Design, Polyamide Dual Layer, ? Np -8 Atm, Rbp – 20 Atm, Entry Profile -0.016,Crossing Profile .70 ? Diameter – 1.25, 1.5, 2.0, 2.25, 2.50, 2.75, 3.00, 3.25, 3.5, 4.00 & 4.5 Mm ? Length –10,12,15,20,25,30, 35, 40 , Ptca Scoring Balloon – Nitinol Helical Shaped Scoring Element – Usfda Approved ? Tapered Tip And Three Nitinol, Helical Shaped, Electropolished Scoring Elements With Rectangular Edges, Mounted On A Balloon With A Larger Working Range Of 2 Atm - 20 Atm ? Lesion Entry Profile .0172, Hydrophilic Coating, Laser Cut Hypotube, Np – 8 Atm, Rbp – 16 Atm ? Diameter -2.0Mm, 2.5Mm, 3.0Mm, 3.5Mm ? Lengths - 6Mm, 10Mm & 15Mm, 20Mm , Ptca Scoring Balloon – Nitinol Helical Shaped Scoring Element – Ce/Dcgi Approved ? Tapered Tip And Three Nitinol, Helical Shaped, Electropolished Scoring Elements With Rectangular Edges, Mounted On A Balloon With A Larger Working Range Of 2 Atm - 20 Atm ? Lesion Entry Profile .0172, Hydrophilic Coating, Laser Cut Hypotube, Np – 8 Atm, Rbp – 16 Atm ? Diameter -2.0Mm, 2.5Mm, 3.0Mm, 3.5Mm ? Lengths - 6Mm, 10Mm & 15Mm, 20Mm , Ptca Scoring Balloon – Triple Triangular Microtome – Pmda Approved ? Scoring Balloon With Triple Triangular Nylon Microtomes 0.0155” In Height With 120-Degree Angle Between Them. ? An Entry Profile Of O.0167 Inch With 2.2Fr Proximal Shaft And 2.6F Distal Shaft. ? Np-14 Atm Rbp Of 24 Atm ? Diameter -2.0Mm, 2.25Mm, 2.5Mm, 2.75Mm, 3.0Mm, 3.25Mm, 3.5Mm, 4.0Mm. ? Length – 13 Mm , Ptca Scoring Balloon Non-Compliant – High Presure - Single Wire – Usfda Approved ? Scoring Balloon With Single Wire Element, Tip Length – 10Mm, Crossing Profile .0350”. ? Slider Hydrophilic Catheter And Silicon Coated Lumen. ? An Entry Profile Of O.0167 Inch With 2Fr Proximal Shaft And 3F Distal Shaft. ? Np-12 Atm Rbp Of 22 Atm, Average Burst Pressure – 30Atm ? Diameter -2.0Mm, 2.25Mm, 2.5Mm, 2.75Mm, 3.0Mm, 3.25Mm, 3.5Mm, 3.75Mm, 4.0Mm. ? Length – 6, 8, 10, 12, 15, 18, 20, 23, 25, 30 Mm , Ptca Scoring Balloon Non-Compliant – High Presure - Single Wire – Ce/Dcgi Approved ? Scoring Balloon With Single Wire Element, Tip Length – 10Mm, Crossing Profile .0350”. ? Slider Hydrophilic Catheter And Silicon Coated Lumen. ? An Entry Profile Of O.0167 Inch With 2Fr Proximal Shaft And 3F Distal Shaft. ? Np-12 Atm Rbp Of 22 Atm, Average Burst Pressure – 30Atm ? Diameter -2.0Mm, 2.25Mm, 2.5Mm, 2.75Mm, 3.0Mm, 3.25Mm, 3.5Mm, 3.75Mm, 4.0Mm. ? Length – 6, 8, 10, 12, 15, 18, 20, 23, 25, 30 Mm , Ptca Cutting Balloon – Usfda Approved ? Bumper Tip, Acrylated Urethane Atherotome Adhesive, Atherotomes , Z-Glide™ Hydrophilic Coating ? Diameter -2.0Mm, 2.25Mm, 2.5Mm, 2.75Mm, 3.0Mm, 3.25Mm, 3.5Mm, 3.75Mm, 4.0Mm. ? Blade Length – 6, 10, 15 Mm , Ptca Cutting Balloon – Ce/Dcgi Approved ? Bumper Tip, Acrylated Urethane Atherotome Adhesive, Atherotomes , Z-Glide™ Hydrophilic Coating ? Diameter -2.0Mm, 2.25Mm, 2.5Mm, 2.75Mm, 3.0Mm, 3.25Mm, 3.5Mm, 3.75Mm, 4.0Mm. ? Blade Length – 6, 10, 15 Mm , Triploblastic Coated Drug Eluting Ptca Balloon - Ce/Dcgi Approved ? Must Have Optimum Concentration Of Sirolimus – 2.75Ug/Mm ? Diameter – 2 - 4Mm, Length - 10 – 30Mm ? Must Have Nominal Pressure 8Atm, Rbp-16Atm , Durg Eluting Pta Balloon For Below The Knee Peripheral Artery-Dcgi Approved Paclitaxel Drug-Coated Pta Balloon Recommended Guide Wire- Otw (Btk): 0.018 Length (Mm): 80,100,120 & 150 Diameter (Mm): 2,2.5,3 & 4 Recommended Guide Wire- Otw (Sfa): 0.035 Length (Mm): 100,120 & 150 Diameter (Mm): 5,6 & 7 , Drug Eluting Ptca Balloon- Us Fda Approved ? All Types & Sizes ? Different Types Of Drugs , Drug Eluting Ptca Balloon- Ce Approved ? All Types & Sizes ? Different Types Of Drugs , Drug Eluting Ptca Balloon- Dcgi Approved ? All Types & Sizes ? Different Types Of Drugs , Balloon Dilatation Catheter For Aorta & Ivc- Us Fda Approved ?Monorail (Rapid Exchange) And Over-The-Wire (Otw) Balloons ?Available In The Sizes And Lengths , Balloon Dilatation Catheter For Aorta & Ivc- Ce Approved ?Monorail (Rapid Exchange) And Over-The-Wire (Otw) Balloons ?Available In The Sizes And Lengths , Balloon Dilatation Catheter For Aorta & Ivc- Dcgi Approved ?Monorail (Rapid Exchange) And Over-The-Wire (Otw) Balloons ?Available In The Sizes And Lengths , Bib (Balloon In Balloon) Type Balloons For Coarctation Dilatation - Us Fda Approved ?Monorail (Rapid Exchange) And Over-The-Wire (Otw) Balloons ?Available In The Sizes And Lengths , Bib (Balloon In Balloon) Type Balloons For Coarctation Dilatation - Ce Approved ?Monorail (Rapid Exchange) And Over-The-Wire (Otw) Balloons ?Available In The Sizes And Lengths , Bib (Balloon In Balloon) Type Balloons For Coarctation Dilatation - Dcgi Approved ?Monorail (Rapid Exchange) And Over-The-Wire (Otw) Balloons Available In The Sizes And Lengths , Z Med Type Balloon For Aortic Coactation – Us Fda/Ce Approved ?5 To 20 Cm Diameter In All Sizes Otw / Rapid Exchange, Compatible With 0.014”/0.035” And 0.038” Wire , Z Med Type Balloon For Aortic Coactation – Dcgi Approved ?5 To 20 Cm Diameter In All Sizes ?Otw / Rapid Exchange, Compatible With 0.014”/0.035” And 0.038” Wire , Z Med Type Balloon For Aortic Coactation – Us Fda/Ce Approved More Than 20 Cm Diameter In All Sizes Otw / Rapid Exchange, Compatible With 0.014”/0.035” And 0.038” Wire , Z Med Type Balloon For Aortic Coactation – Dcgi Approved ?More Than 20 Cm Diameter In All Sizes ?Otw / Rapid Exchange, Compatible With 0.014”/0.035” And 0.038” Wire , Proximal Optimization Balloon – Usfda Approved ? Specialised Proximal Optimisation Balloon Dilatation Catheter With Ultra Short Balloon Shoulder Of 0.6Mm And An Rbp Of 22 Atm With Sizes Ranging From A Length Of 6-15 Mm And Diameters Ranging From 2.25-5 Mm. Hydrophilic External Surface Coating From Tip To Adjacent Guidewire Port And Silicone Coating Inside Guidewire Lumen. , Proximal Optimization Balloon – Ce/Dcgi Approved ? Specialised Proximal Optimisation Balloon Dilatation Catheter With Ultra Short Balloon Shoulder Of 0.6Mm And An Rbp Of 22 Atm With Sizes Ranging From A Length Of 6-15 Mm And Diameters Ranging From 2.25-5 Mm. Hydrophilic External Surface Coating From Tip To Adjacent Guidewire Port And Silicone Coating Inside Guidewire Lumen. , Ptca High Pressure Cto Balloon – Usfda Approved ? 0.75 Mm Cto Balloon With A Tip Entry Profile Of 0.015” And Ultra Low Crossing Profile Of 0.020” With A Proprietary Distal Welding Technology, 2.2F Distal Shaft, Rated Burst Pressure Of 20 Atm And Average Burst Pressure Of = 28 Atm. ? Diameters From 0.75Mm, 1.0Mm, 1.25Mm, 1.50Mm, 1.75Mm & 2.0Mm ? Lengths From 5Mm, 8Mm, 10Mm, 15Mm, 20Mm, 25Mm & 30Mm. , Ptca High Pressure Cto Balloon – Ce/Dcgi Approved ? 0.75 Mm Cto Balloon With A Tip Entry Profile Of 0.015” And Ultra-Low Crossing Profile Of 0.020” With A Proprietary Distal Welding Technology, 2.2F Distal Shaft, Rated Burst Pressure Of 20 Atm And Average Burst Pressure Of = 28 Atm. ? Diameters From 0.75Mm, 1.0Mm, 1.25Mm, 1.50Mm, 1.75Mm & 2.0Mm ? Lengths From 5Mm, 8Mm, 10Mm, 15Mm, 20Mm, 25Mm & 30Mm. , Rotalink Burr - Us Fda Approved (Compatible With Existing Rota Machine Cath Lab Gmc Kots). , Rotalink Burr – Dcgi Approved (Compatible With Existing Rota Machine Cath Lab Gmc Kota). , Rotalink Advancer - Us Fda Approved (Compatible With Existing Rota Machine Cath Lab Gmc Kota). , Rotalink Advancer - Ce Approved (Compatible With Existing Rota Machine Cath Lab Gmc Kota). , Rotalink Advancer – Dcgi Approved (Compatible With Existing Rota Machine Cath Lab Gmc Kota). , Rotalink Plus (Advancer & Burr) - Us Fda Approved (Compatible With Existing Rota Machine Cath Lab Gmc Kota ). , Rotalink Plus (Advancer & Burr) - Ce Approved (Compatible With Existing Rota Machine Cath Lab Gmc Kota , Rotalink Plus (Advancer And Burr) – Dcgi Approved (Compatible With Existing Rota Machine Cath Lab Gmc Kota , Rotational Atherectomy Guide Wires - Us Fda Approved , Rotational Atherectomy Guide Wires - Ce Approved , Rotational Atherectomy Guide Wires –Dcgi Approved , Rotaglide Lubricant - Us Fda Approved , Rotaglide Lubricant - Ce Approved , Rotaglide Lubricant – Dcgi Approved , Rotawire – Us Fda Approved Should Be Compatible To Rota Machine In Cath Lab Gmc Kota , Rotawire – Dcgiapproved Should Be Compatible To Rota Machine In Cath Lab Gmc Kota. , Heart Pump Catheter And Smartassist Sensor ? Usfda & Ce Approved Percutaneous Heart Pump Capable Of Pumping Blood @ 3.5-5 L/Min To Provide Hemodynamic Support For Hemodynamic Stabilization To Enable Heart Recovery. Maintain Patient Hemodynamics During Planned Temporary Coronary Occlusions By Maintaining Mean Arterial Pressure (Map), Which May Allow For A More Thorough Procedure And A More Complete Revisualization Ma Single Session. , Nirs+Ivus Catheter ? Usfda & Japan Pmda Approved Near Infrared Spectroscopy & Intravascular Imaging Catheter For Detection Of Lipid Core Plaques (Lcp) And Assessment Of Vessel Structure With An Automatically Adjustable Frequency Bandwidth Of 35-65 Mhz Depending On The Need Of The Calcium With A Pullback Speed Upto 2Mm/Sec And A Pullback Length If 150 Mm. Catheter Working Length Of 160 Cm , Ivus Catheter With Accessories - Usfda Approved ? Compitable To Volcano Imaging Machine In Cath Lab, Govt.Medical College Kota- , Ivus Catheter With Accessories - Ce/Dcgi Approved ? Compitable To Volcano Imaging Machine In Cath Lab, Govt.Medical College Kota- , Shockwave I.V.L Intravascularlithotripsy Catheter System With Connector Cable - Dcgi With Us Fda / Ce Approved , I.V.L Indegenous Intravascularlithotripsy Catheter System With Connector Cable – Dcgi , Ivus Catheter Hd 60 Mhz Coronary Imaging Catheters. - Us Fda Approved Should Be Compatible With Available Machine , Ivus Catheter Hd 60 Mhz Coronary Imaging Catheters. – Ce/Dcgi Approved Should Be Compatible With Available Machine , Ivus Catheter40 Mhz Coronary Imaging Catheters. - Us Fda Approved Should Be Compatible With Available Machine , Ivus Catheter40 Mhz Coronary Imaging Catheters. - Us Fda Approved Should Be Compatible With Available Machine , Laser Atherectomy Catheter X-80 Catheters With Guidewire Compatanility Of 0.014 Inch , Guiding Catheter Compatability Of 6F, Maximum Tip Outer Diameter Ofm 0.038Inch , Maximum Shaft Outer Diameter Of 0.049 Inchwith A Working Length Of 100 Mm , Capability To Generate A Fluence Of 30- 80 Mj/Mm2 With A Repitation Rate Of 25-80 Hertz. Available In 0.9 Mm And 1.4 Mm Sizes. , Fractional Flow Reserve Pressure Wire 1. Shouldbe0.014”Guidewire. 2. Should Have High-Fidelity Piezo Electric Pressure Sensor Technology For Measurement Of Intravascular Pressure. 3. The System Should Work Wireless Radio Using Frequency-Hopping Spread Spectrum To Ensure Secured Radio Connection With Pressurewire 4. Thepressurewireshouldbecapableofwiredconnectiontoffrmachine. 5. Shouldhavesensorhousingdesignwithmultiplelargewindows(Multiwindow Jacket). 6. Shouldhaveaflatcoretipdesignforabettershapeability&Shaperetention. 7. Shouldpreferablyhavehydrophiliccoating 8. Shouldhavearadioopaquetip. 9. Shouldhaveoperatingpressurerangeof-30To+300Mmhg. 10.Should Have Frequency Response Of Dc To 25 Hz. 11.Should Have Radio Range Of At Least 2M. 12.Should Have Battery Time Of Transmitter For At Least 3 Hours. 13.Should Have A Wireless Transmission Frequency Range Of 2.4000 – 2.4835 Ghz , Oct Catheter: Catheter For Intracoronary Oct, 0.014 Guidewire And 6 F Guide Catheter Compatibility. Lubricous Hydrophilic Coating And Low Tip Entry Profile For Crossing Tight, Distal Lesions.2.7 F Crossing Profile And Supportive Proximal Shaft Provide Superb Deliverability To The Area Of Interest. Lens Marker Is Immediately Proximal To Imaging Lens And The Distance Of Lens Marker From Tip Should Be 23 Mm And Proximal Marker At 82 Mm From The Lens Marker. Threeradiopaque Marker , Temporary Bipolar Pacing Catheter- Flow Directed 1. Should Be Us Fda & Dcgi Approved 2. Should Be Latex Balloon Tipped, Flow Guided For Stable Insertion. 3. Should Have 10 Cm Depth Markers To Enhance Placement. 4. Should Have Smooth, Polyurethane Hemocompatible Coating. 5. Should Have Clearly Marked Terminals. 6. Should Have Shrouded 2 Mm Pin Connector Leads. 7. Should Have Platinum Electrodes 8. It Should Have Flexible Tip Design For Delicate Placement. , Temporary Bipolar Pacing Catheter- Torque Control 1. Should Be Us Fda & Dcgi Approved 2. Should Have 10 Cm Depth Markers To Enhance Placement. 3. Should Have Smooth, Polyurethane Hemocompatible Coating. 4. Should Have Clearly Marked Terminals. 5. Should Have Shrouded 2 Mm Pin Connector Leads. 6. Should Have Stainless Steel Centre Conductor And Stainless Steel Electrodes. 7. It Should Have Solid Core Enables User To Customize The Curve. 8. Should Have Optimal Torque Control For Challenging Anatomy , Orbital Atherectomy Device 6F Compatible Orbital Atherectomy Device With 1.25Mm Diamond Coated Crown Designed For Bidirectional Superficial Calcium Sanding And Modify Deep Calcium Through Pulsatile Forces To Facilitates Stent Delivery And Expansion In Severely Calcified Lesions With Durable Nitinol Guidewire With 0.12” Proximal And 0.14” Distal End Along With Viper Slide Lubricant , Oas Pump Provides The Saline Pumping Mechanism And Power To The Oad With 250 V 4A Slow Blow, 1/4” X 1 - 1¼” Meter Fuse, Abs Plastic External Housing, (100–240 Vac @ 50–60 Hz) External Connector. Includes A Bult In Audible Information Signal For Approximately Every 25 Sec Of Oad Spin Time. Audible Information Signal Every 5 Sec For A Total Of 30 Sec When The Saline Level Falls Below 200 Ml.During A Treatment Period. The Small, Reusable, And Portable Oas Pump Attaches To A Standard Five-Wheel Rolling Intravenous (Iv) Pole Or Table Mount Pole. , Pressure Wire For Ffr/Dfr – Usfda , Pressure Wire For Ffr/Dfr – Ce/Dcgi , Iabp Catheter With Accessories - Us Fda Approved Should Be Compatible With Existing Machine (Data Scope) In Cath Lab, Gmck , Iabp Catheter With Accessories - Ce Approved Should Be Compatible With Existing Machine (Data Scope) In Cath Lab, Gmck , Iabp Catheter With Accessories Dcgi Approved Should Be Compatible With Existing Machine (Data Scope) In Cath Lab, Gmck , Tpi Lead – Usfda Approved , Tpi Lead – Ce Approved , Tpi Lead – Dcgi Approved , Vascular Closure Device With Bio Absorbable Pga Suture That Provide A Secure Seal •Bioabsorbable Collagen Designed, •Low Profile Bioabsorbable Anchor (50:50 Blend Glycolide And Lactide Polyer) •Must Have Bovine Collagen Plug. Must Have 9 Hole V-Twist Pattern Suture Weave. •Must Be Available In 6F And 8F Sizes. Usfda+Pmda Approved , Vascular Closure Device With Bio Absorbable Pga Suture That Provide A Secure Seal •Bioabsorbable Collagen Designed, •Low Profile Bioabsorbable Anchor (50:50 Blend Glycolide And Lactide Polyer) •Must Have Bovine Collagen Plug. Must Have 9-Hole V-Twist Pattern Suture Weave. •Must Be Available In 6F And 8F Sizes. Ce/Dcgi Approved , Everolimus Eluting Cobalt Chromium Stent – Usfda Approved ? Everolimus Eluting Cobalt Chromium Stent With Peak To Valleynon-Linear Links With Narrower And Slimmer Crests And Ultra- Low Crossing Profile Of 0.039 Inches For Precise Placement And Zero Transition Distal Shaft. Should Have Flourinated Co- Polymer. Should Come In Diameters From 2.00 Mm To 4.00 Mm With 5.5 Mm Post-Dilatation Capability For 3.5 Mm And 4.0 Mm Stents , Everolimus Eluting Cobalt Chromium Stent – Ce/Dcgi Approved ? Everolimus Eluting Cobalt Chromium Stent With Peak To Valley Non Linear Links With Narrower And Slimmer Crests And Ultra-Low Crossing Profile Of 0.039 Inches For Precise Placement And Zero Transition Distal Shaft. Should Have Flourinated Co-Polymer. Should Come In Diameters From 2.00 Mm To 4.00 Mm With 5.5 Mm Post-Dilatation Capability For 3.5 Mm And 4.0 Mm Stents , Everolimus Eluting Cobalt Chromium Stent – Usfda Approved ? Everolimus Eluting Cobalt Chromium Stent With Peak To Valley Taller Non Linear Links And True Centre Tip Technology For Precise Placement And Zero Transition Distal Shaft. Should Have Flourinated Co-Polymer. Should Come In Diameters From 2.00 Mm To 4.00 Mm , Everolimus Eluting Cobalt Chromium Stent – Ce/Dcgi Approved ? Everolimus Eluting Cobalt Chromium Stent With Peak To Valley Taller Non Linear Links And True Centre Tip Technology For Precise Placement And Zero Transition Distal Shaft. Should Have Flourinated Co-Polymer. Should Come In Diameters From 2.00 Mm To 4.00 Mm , Everolimus Eluting Cobalt Chromium Stent – Usfda Approved ? Everolimus Eluting Cobalt Chromium Stent With Peak To Valley Taller Non Linear Links And 5 Fold Balloon Technology And Should Have Flourinated Co Polymer. Skive Technology To Have A Better Pushability. Should Come In Diameters From 2.00 Mm To 4.00 Mm. , Everolimus Eluting Cobalt Chromium Stent – Ce/Dcgi Approved ? Everolimus Eluting Cobalt Chromium Stent With Peak To Valley Taller Non Linear Links And 5 Fold Balloon Technology And Should Have Flourinated Co Polymer. Skive Technology To Have A Better Pushability. Should Come In Diameters From 2.00 Mm To 4.00 Mm. , Everolimus Eluting Cobalt Chromium Stent – Logn Length Usfda Approved ? Everolimus Eluting Cobalt Chromium Stent With Peak To Valley Taller Non Linear Links And 5 Fold Balloon Technology And Should Have Flourinated Co Polymer. Skive Technology To Have A Better Pushability. Should Come In Diameters From 2.00 Mm To 4.00 Mm Upto 48 Mm Length. , Everolimus Eluting Cobalt Chromium Stent – Logn Length - Ce Approved ? Everolimus Eluting Cobalt Chromium Stent With Peak To Valley Taller Non Linear Links And 5 Fold Balloon Technology And Should Have Flourinated Co Polymer. Skive Technology To Have A Better Pushability. Should Come In Diameters From 2.00 Mm To 4.00 Mm Upto 48 Mm Length. , Everolimus Eluting Cobalt Chromium Stent – Usfda Approved ? Usfda Approved Everolimus Eluting Cobalt Chromium Stent With Peak To Valley Taller Non Linear Links And Dual Layer Pebax Balloon Technology And Should Have Flourinated Co Polymer. Ss Junction Support Mandrel To Have A Better Pushability. Should Come In Diameters From 2.00 Mm To 4.00 Mm. , Everolimus Eluting Cobalt Chromium Stent – Ce/Dcgi Approved ? Usfda Approved Everolimus Eluting Cobalt Chromium Stent With Peak To Valley Taller Non Linear Links And Dual Layer Pebax Balloon Technology And Should Have Flourinated Co Polymer. Ss Junction Support Mandrel To Have A Better Pushability. Should Come In Diameters From 2.00 Mm To 4.00 Mm. , Everolimus Eluting Platinum Chromium Stent - Durable Polymer– Usfda Approved , Everolimus Eluting Platinum Chromium Stent - Durable Polymer – Ce/Dcgi Approved , Everolimus Eluting Platinum Chromium Stent – Biodegradable Polymer - Ce/Dcgi Approved , Everolimus Eluting Platinum Chromium Stent – Biodegradable Polymer -Ce/Dcgi Approved , Sirolimus Eluting Cobalt-Chromium Stent With Abluminal Gradient Coating - (L-605 Co-Cr Alloy) – Usfda/Pmda (Should Not Have Drug & Polymer Coating On Joints & Bends). 2 Links – 8 Crown Design •Bioresorbable Polymer Of Plcl (Poly Lactic Acid + Poly Capro Lactone Pcl) With Degradation Time Of 3-4 Months. Should Have Bioinspired Open Cell In Phase Design. •Low Concentration Of Sirolimus (0.8Ug/Mmsq). •Minimum Tip Entry Profile Of 0.42Mm , Sirolimus Eluting Cobalt-Chromium Stent With Abluminal Gradient Coating - (L-605 Co-Cr Alloy) – Ce/Dcgi (Should Not Have Drug & Polymer Coating On Joints & Bends). 2 Links – 8 Crown Design •Bioresorbable Polymer Of Plcl (Poly Lactic Acid + Poly Capro Lactone Pcl) With Degradation Time Of 3-4 Months. Should Have Bioinspired Open Cell In Phase Design. •Low Concentration Of Sirolimus (0.8Ug/Mmsq). Minimum Tip Entry Profile Of 0.42Mm , Optimized Overexpansion, Up To 6.25 Mm For Large Vessel- Sirolimus Eluting Cobalt-Chromium Stent With Advanced Core Wire Shaft Technology & Abluminal Gradient Coating - (L-605 Co-Cr Alloy) – Usfda/Pmda ? Should Not Have Drug & Polymer Coating On Joints & Bends. 2 Links – 8 & 10 Crown Design ? Must Have Advanced Core Wire Shaft Technology. ? Should Have An Over Expansion Limit Of More Than 1.5 Mm Of The Stated Diameter ? Must Have Rounded & Flexible Tip Made Up Of Polyamide Elastomer. ? Bioresorbable Polymer Of Plcl (Poly Lactic Acid + Poly Caprolactone Pcl) With Degradation Time Of 3-4 Months. Should Have Bioinspired Open Cell In Phase Design. Low Concentration Of Sirolimus (0.8Ug/Mmsq), Tip Entry Profile Of 0.42Mm. , Optimized Overexpansion, Up To 6.25 Mm For Large Vessel- Sirolimus Eluting Cobalt-Chromium Stent With Advanced Core Wire Shaft Technology & Abluminal Gradient Coating - (L-605 Co-Cr Alloy) – Ce/Dcgi ? Should Not Have Drug & Polymer Coating On Joints & Bends. 2 Links – 8 & 10 Crown Design ? Must Have Advanced Core Wire Shaft Technology. ? Should Have An Over Expansion Limit Of More Than 1.5 Mm Of The Stated Diameter ? Must Have Rounded & Flexible Tip Made Up Of Polyamide Elastomer. ? Bioresorbable Polymer Of Plcl (Poly Lactic Acid + Poly Caprolactone Pcl) With Degradation Time Of 3-4 Months. Should Have Bioinspired Open Cell In Phase Design. Low Concentration Of Sirolimus (0.8Ug/Mmsq), Tip Entry Profile Of 0.42Mm. , Sirolimus Eluting With Probio Coating Stent – Usfda Approved Sirolimus Eluting Cobalt Chromium Stents, Ultrathin Struts 60 Um. Should Have Coating Passive Probio Coating (Amorphous Silicon Carbide). Should Have Active Coating Bio Lute Bioabsorbable Ploy-L-Lactide. Should Be Usfda Approved. , Sirolimus Eluting With Probio Coating Stent – Ce/Dcgi Approved Sirolimus Eluting Cobalt Chromium Stents, Ultrathin Struts 60 Um. Should Have Coating Passive Probio Coating (Amorphous Silicon Carbide). Should Have Active Coating Bio Lute Bioabsorbable Ploy-L-Lactide. Should Be Usfda Approved. , Sirolimus Eluting With Silicon Carbide Coating Stent – Usfda Approved Sirolimus Eluting Cobalt Chromium Stents With Amorphous Silicon Carbide Coating. Should Be Usfda Approved. , Sirolimus Coated Stainless Steel Stent – Ce Approved ?Porus Surface, Shellac Resin (Wax-Free), Bioresorbable Polymer , Sirolimus Eluting Cobalt Chromium Platform, - Us Fda / Ce Approved ? Biodegradable Polymer, And Microporus ? Surface With Soft Coating Of Shellac Rasin. , Sirolimus Cluting, Stainless Steel Platform, - Us Fda / Ce Approved ? Biodegradable Polymer, Microporus Surfacewith Soft Coating Of Shellac Rasin With Temperature Control Packing & Temperature ? Sensitive Check Meter. , Dual Drug Polymer Free Drug Eluting Stent - Dcgi With Us Fda /Ce Approved ? Should Have Cobalt Chromium Platform With Prubocol Drug At Place Of Polymer. ? Should Have No Polymer. ? Abluminal Coating On Microporus Surface With Soft Coating Of Shellac Rasin. , Dual Drug Polymer Free Drug Eluting Stent - Dcgi Approved ? Should Have Cobalt Chromium Platform With Prubocol Drug At Place Of Polymer. ? Should Have No Polymer. Abluminal Coating On Microporus Surface With Soft Coating Of Shellac Rasin. , Bio-Resorbable Scaffold (Brs) ? Sirolimus Eluting Bio-Resorable Scaffold Stent System - Dcgi With Us Fda / Ce Approved ? All Sizes And Diameter , Sirolimus Coated Drug Stent - Ce Approved • Open Cell Design Only With Two Connectors Between The Rings, Stent Material: Cocr Per Astm F562 • 60? Ultra-Thin Struts Across All Diameters And Lengths • Crossing Profile Of = 0.97Mm Tip Entry Profile: 0.017”, Ldz Link: Long Dual ‘Z’ Link • Rbp: 16 Atm • Length (Mm): 8 To 48 Mm • Diameter(Mm): 2.25 To 4.00 Mm , Sirolimus Coated Drug Stent - Dcgi Approved • Open Cell Design Only With Two Connectors Between The Rings, Stent Material: Cocr Per Astm F562 • 60? Ultra-Thin Struts Across All Diameters And Lengths • Crossing Profile Of = 0.97Mm Tip Entry Profile: 0.017”, Ldz Link: Long Dual ‘Z’ Link • Rbp: 16 Atm • Length (Mm): 8 To 48 Mm • Diameter(Mm): 2.25 To 4.00 Mm , Everolimus Coated Drug Eluting Cobalt Chromium Coronary Stent - Dcgi Approved • Everolimus Drug Eluting Stent, Open Cell Design Only With Two Connectors Between The Rings • Stent Material & Design: L-605 Co-Cr Alloy With Laser Cut Seamless Tubing In Serpentine Pattern. • 60? Ultra-Thin Struts Across All Diameters And Lengths, Crossing Profile Of = 0.97Mm, Tip Entry Profile: 0.017” • Ldz Link: Long Dual ‘Z’ Link, Ifu Labeled Overexpansion Of The Highest Available Diameter Should Be = 5.50 Mm • Rbp: 16 Atm • Length (Mm): 8 To 48 Mm • Diameter(Mm): 2.25 To 4.00 Mm , Sirolimus Coated Drug Stent Ce Approved • Open Cell Design Only With Two Connectors Between The Rings • Stent Material & Design: L-605 Co-Cr Alloy With Laser Cut Seamless Tubing In Serpentine Pattern. • 60? Ultra-Thin Struts Across All Diameters And Lengths -Long Link Design • Crossing Profile Of = 0.97Mm,M Tip Entry Profile: 0.41Mm • Rbp: 16 Atm • Length (Mm): 8 To 48 Mm • Diameter(Mm): 2.25 To 4.00 Mm , Sirolimus Coated Drug Stent Dcgi Approved • Open Cell Design Only With Two Connectors Between The Rings • Stent Material & Design: L-605 Co-Cr Alloy With Laser Cut Seamless Tubing In Serpentine Pattern. • 60? Ultra-Thin Struts Across All Diameters And Lengths -Long Link Design • Crossing Profile Of = 0.97Mm,M Tip Entry Profile: 0.41Mm • Rbp: 16 Atm • Length (Mm): 8 To 48 Mm • Diameter(Mm): 2.25 To 4.00 Mm , Covered Stent Usfda Approved , Covered Stent Ce/Dcgi Approved , Covered Coronary Stents - Us Fda Approved , Covered Coronary Stents – Ce/Dcgi Approved Covered Graft Stent For Dissected Artery , Guidewire For Peripheral Intervention – Nitinol Alloy Regular Length ? Tip Load Options Of 6 G, Nitinol Lengths Of 10 Cm , Guidewire For Peripheral Intervention – Nitinol Alloy Regular Length ? Tip Load Options Of 4 G, Nitinol Lengths Of 25 Cm , Guidewire For Peripheral Intervention – Nitinol Alloy Regular Length– ? Tip Load Options Of 3.5 G, Nitinol Lengths Of 40 Cm , Guidewire For Peripheral Intervention – Nitinol Alloy Regular Length– ? Tip Load Options Of 2.8 G, Nitinol Lengths Of 40 Cm , Guidewire For Peripheral Intervention – Stainless Steel, Regular Length ? .018Short Taper, Bare Coil, Core To Tip, Tip Load – 4.6 Gm , Pta Balloon – 12-200Mm - Usfda ? Diameters 1.5, 2.0, 2.5, 3.0, And 4.0 Mm, Length – 12, 20, 40, 60, 80, 120, 200 ? 4F Sheath Compatible, Hydrophilic Coating, Tungsten Markers, Np- 8, Rbp - 14 , Pta Balloon - 12-200Mm – Ce/Dcgi ? Diameters 1.5, 2.0, 2.5, 3.0, And 4.0 Mm, Length – 12, 20, 40, 60, 80, 120, 200 ? 4F Sheath Compatible, Hydrophilic Coating, Tungsten Markers, Np- 8, Rbp - 14 , Pta Balloon – 20-200Mm - Usfda Approved ? Diameters 2.0, 2.5, 3.0, 4.0, 5.0, 5.5, 6.0, Length – 20, 40, 60, 80, 120, 150, 180, 200 ? 4F/5F Sheath Compatible, Hydrophilic Coating, Tungsten Markers, Np- 8, Rbp – 14 ? Coaxial, Over-The-Wire Design,One-Piece Catheter Construction,Hydrophobic Coating , Pta Balloon – 20-200Mm Ce/Dcgi ? Diameters 2.0, 2.5, 3.0, 4.0, 5.0, 5.5, 6.0, Length – 20, 40, 60, 80, 120, 150, 180, 200 ? 4F/5F Sheath Compatible, Hydrophilic Coating, Tungsten Markers, Np- 8, Rbp – 14 ? Coaxial, Over-The-Wire Design,One-Piece Catheter Construction,Hydrophobic Coating , Pta Balloon – 20-250Mm - Usfda ? Diameters 3 -12 Mm, Length – 20, 40, 60, 80, 120, 150, 200, 250 ? 5-7 F Sheath Compatible, Hydrophilic Coating, Tungsten Markers, , Pta Balloon – 20-250Mm – Ce/Dcgi ? Diameters 3 -12 Mm, Length – 20, 40, 60, 80, 120, 150, 200, 250 ? 5-7 F Sheath Compatible, Hydrophilic Coating, Tungsten Markers, , Pta Balloon – 15-40Mm – Usfda ? Diameters 4 -7 Mm, Lengths Of 15 Mm, 20 Mm, 30 Mm, And 40 Mm ? Xcelon Balloon Material With A 14 Atm Rbp,Hydrophobic Coated Shaft And Balloon,Np- 8, Rbp – 14 , Pta Balloon – 15-40Mm – Ce/Dcgi ? Diameters 4 -7 Mm, Lengths Of 15 Mm, 20 Mm, 30 Mm, And 40 Mm Xcelon Balloon Material With A 14 Atm Rbp,Hydrophobic Coated Shaft And Balloon,Np- 8, Rbp – 14 , Pta Balloon Dilatation Catheter – Usfda ? Diameters 3 -12 Mm, Length – 20, 30, 40, 60, 80, 100, 120, 150, 200 -? Up To 24 Atm (2431 Kpa) Rated Burst Pressure ? Nybax Balloon Material, 3 Wings On 3-5 Mm, 5 Wings On 6 Mm And Plus, Mediglide Hydrophilic Coating , Pta Balloon Dilatation Catheter – Ce/Dcgi ? Diameters 3 -12 Mm, Length – 20, 30, 40, 60, 80, 100, 120, 150, 200 ? Up To 24 Atm (2431 Kpa) Rated Burst Pressure Nybax Balloon Material, 3 Wings On 3-5 Mm, 5 Wings On 6 Mm And Plus, Mediglide Hydrophilic Coating , Ultra-High-Pressure Balloon -With Pressures Up To 40 Atm - Usfda ? Diameters 4 -12 Mm, Length – 20, 30, 40, 60, 80, 100 - ? Up To 40 Atmrated Burst Pressure , Ultra-High-Pressure Balloon -With Pressures Up To 40 Atm -Ce/Dcgi ? Diameters 4 -12 Mm, Length – 20, 30, 40, 60, 80, 100 Up To 40 Atmrated Burst Pressure , 0.018” Balloon Dilatation Catheter - Usfda ? 0.020” Lesion Entry Profile On A 0.018” Wire ? 2-10 Mm Diameters, 10-220 Mm Lengths , 0.018” Balloon Dilatation Catheter -Ce/Dcgi ? 0.020” Lesion Entry Profile On A 0.018” Wire 2-10 Mm Diameters, 10-220 Mm Lengths , 0.035” Balloon Dilatation Catheter -Usfda ? 0.020” Lesion Entry Profile On A 0.018” Wire ? 12, 14, 16, 18 Mm Diameters, 20, 40, 60 Mm Lengths , 0.035” Balloon Dilatation Catheter -Ce/Dcgi ? 0.020” Lesion Entry Profile On A 0.018” Wire 12, 14, 16, 18 Mm Diameters, 20, 40, 60 Mm Lengths , 0.014” Balloon Dilatation Catheter -Usfda ? 0.017 Lesion Entry Profile, Nybax Balloon Material , 0.014” Balloon Dilatation Catheter -Ce/Dcgi 0.017 Lesion Entry Profile, Nybax Balloon Material , Cutting Balloon For Renal And Peripheral Arteries - Us Fda Approved ?Monorail (Rapid Exchange) And Over-The-Wire (Otw) Balloons Available In The Sizes And Lengths , Cutting Balloon For Renal And Peripheral Arteries - Ce Approved ?Monorail (Rapid Exchange) And Over-The-Wire (Otw) Balloons Available In The Sizes And Lengths , Cutting Balloon For Renal And Peripheral Arteries - Dcgi Approved ?Monorail (Rapid Exchange) And Over-The-Wire (Otw) Balloons Available In The Sizes And Lengths , Otw Balloon For Periferal Angioplasty All Size And Diameters- Ce/ Fda Approved , Otw Balloon For Periferal Angioplasty All Size And Diameters- Dcgi Approved , Btk Everolimus Eluting Resorbable Scaffold System – Usfda , Btk Everolimus Eluting Resorbable Scaffold System – Ce/Dcgi , Peripheral Self Expandable Interwoven Nitinol Stent Forsuperficial Femoral Artery (Sfa) And / Or Proximal Popliteal Artery- Usfda Approved , Peripheral Self Expandable Interwoven Nitinol Stent Forsuperficial Femoral Artery (Sfa) And / Or Proximal Popliteal Artery- Dcgi/Ce Approved , Self-Expanding Peripheral Stent – Usfda Approved ? Tri-Axial Technology Specifications, Flexible Nitinol Material , Self-Expanding Peripheral Stent – Ce/Dcgi Approved ? Tri-Axial Technology Specifications, Flexible Nitinol Material , Balloon-Expanding Peripheral Stent – Usfda Approved ? Cobalt Chromium Multi-Link Technology, Dual-Layer Balloon , Balloon-Expanding Peripheral Stent – Usfda Approved ? Cobalt Chromium Multi-Link Technology, Dual-Layer Balloon , Renal Stent System – Usfda Approved ? Cobalt Chromium Multi-Link Technology , Renal Stent System – Ce/Dcgi Approved Cobalt Chromium Multi-Link Technology , Carotid Stent – Usfda ? Closed-Cell Design For Crush Resistance,Rotational Deployment Handle With Freestyle,U- And S-Shaped Connectors , Carotid Stent – Ce/Dcgi ? Closed-Cell Design For Crush Resistance,Rotational Deployment Handle With Freestyle,U- And S-Shaped Connectors , Carotid Stent – Usfda Straight And Tapered Stent Options, Nitinol Material , Carotid Stent – Ce/Dcgi Closed-Cell Design For Crush Resistance,Rotational Deployment Handle With Freestyle,U- And S-Shaped Connectors , Embolic Protection System – Usfda Centered Wire Design, Circumferential Nitinol Frame, Platinum-Tungsten Frame Coils, Barewir Technology , Embolic Protection System – Ce/Dcgi Centered Wire Design, Circumferential Nitinol Frame, Platinum-Tungsten Frame Coils, Barewir Technology , Vascular Plug – Single Lobe , Vascular Plug- Multi-Layered Mesh Designed, Six Planes Of Cross Sectional Coverage , Suture-Mediated Closure And Repair System – Usfda Approved , Suture-Mediated Closure (Smc) For Both Arterial And Venous Access – Usfda , Suture-Mediated Closure (Smc) For Both Arterial And Venous Access – Ce/Dcgi , Renal And Biliary Premounted Stent System – Usfda Macr Elements And Additional Proximal Connectors , Renal And Biliary Premounted Stent System – Ce/Dcgi Macr Elements And Additional Proximal Connectors , Drug Coated Balloon For Pta – Usfda Transpax Coating,Paclitaxel-Coated Pta Balloon Catheter , Drug Coated Balloon For Pta – Usfdace/Dcgi Transpax Coating,Paclitaxel-Coated Pta Balloon Catheter , Carotid Stent – Usfda Approved Closed Cell Design, , Carotid Stent – Ce/Dcgi Approved Closed Cell Design, , Iliac And Biliary Premounted Stent System – Usfda Macro Elements Engineered , Iliac And Biliary Premounted Stent System – Ce/Dcgi Macro Elements Engineered , Renal And Biliary Premounted Stent System – Usfda Tandem Architectur Stent Design , Renal And Biliary Premounted Stent System – Ce/Dcgi Tandem Architectur Stent Design , Self Expanding Peripheral Stent – Usfda Approved , Peripharel Drug-Eluting Vascular Stent -Usfda , Peripharel Drug-Eluting Vascular Stent -Ce/Dcgi , Self-Expanding Stent System For Iliac – Usfda , Self-Expanding Stent System For Iliac – Ce/Dcgi , Distal Protection Device 0.014 Wire Umbrella Type Coronary Filter - Us Fda/Ce Approved , Distal Protection Device 0.014 Wire Umbrella Type Coronary Filter - Dcgi Approved , Distal Protection Device 0.014 Wire Umbrella Type Carotid Artery Filter - Us Fda/Ce Approved , Distal Protection Device 0.014 Wire Umbrella Type Carotid Artery Filter - Dcgi Approved , Embolic Protection Devices Based On Filter Technology/Mechanism - Us Fda Approved , Embolic Protection Devices Based On Filter Technology/Mechanism - Dcgi Approved , Embolic Protection Devices With Distal Balloon Occlusive Techonology - Us Fda Approved , Embolic Protection Devices With Distal Balloon Occlusive Techonology-Ce Approved , Embolic Protection Devices With Distal Balloon Occlusive Techonology - Dcgi Approved , Distal Embolic Protection Device - Us Fda Approved ? Should Be Made Of Polyurethane With Radio-Opaque Nitinol Loop ?Should Be Suspended On The .014” Wire With A Suspension Arm. ?Should Not Occlude Flow While In Placement, Should Be Rapid Exchange Type ? Should Be Compatible With A 6 F Guiding Catheter (0.066” Id) Should Allow Optimal Filtration In Vessels 3.5 - 5.5 Mm Size , Distal Embolic Protection Device – Ce/Dcgi Approved ? Should Be Made Of Polyurethane With Radio-Opaque Nitinol Loop ?Should Be Suspended On The .014” Wire With A Suspension Arm. ?Should Not Occlude Flow While In Placement, Should Be Rapid Exchange Type ? Should Be Compatible With A 6 F Guiding Catheter (0.066” Id) Should Allow Optimal Filtration In Vessels 3.5 - 5.5 Mm Size , Peripheral Cutting Balloon Catheter - Us Fda Approved ? Should Be Available In Balloon Od Of 3-6 Mm ? Should Have Up To 15 Mm Or Up To 20 Mm Working Length , Peripheral Cutting Balloon Catheter – Ce/Dcgi Approved ? Should Be Available In Balloon Od Of 3-6 Mm ? Should Have Up To 15 Mm Or Up To 20 Mm Working Length Catheter Shaft Length Should Be Up To 140 Cm , Balloon In Balloon Catheter (Bib)- Dcgi With Us Fda /Ce Approved , Plaque Modification Device For Highly Calcified Lesions - Dcgi With Us Fda / Ce Approved ? Available In The Sizes And Length ? Should Be Along With Support Accessories ? Super High Pressure Balloon Dialation Catheter Non Compliant Rbp -35 Bar Must Be Twin Layer In Balloon With Low Lesion Entry Profile”0.16” , Ivc Filter – Us Fda Approved ?For Optimal Filtration Of Ivc Diameter Of Up To 40 Mm ?Made Of Either Nitinol Or Stainless Steel ?Catheter Carrier System Inner Diameter Should Be Of Maximum 12 F ?It Should Be Possible To Insert From Either Jugular Or Femoral Access Should Be For Permanent Use , Ivc Filter – Ce Approved ?For Optimal Filtration Of Ivc Diameter Of Up To 40 Mm ?Made Of Either Nitinol Or Stainless Steel ?Catheter Carrier System Inner Diameter Should Be Of Maximum 12 F ?It Should Be Possible To Insert From Either Jugular Or Femoral Access Should Be For Permanent Use , Ivc Filter – Dcgiapproved ?For Optimal Filtration Of Ivc Diameter Of Up To 40 Mm ?Made Of Either Nitinol Or Stainless Steel ?Catheter Carrier System Inner Diameter Should Be Of Maximum 12 F ?It Should Be Possible To Insert From Either Jugular Or Femoral Access Should Be For Permanent Use , Endovascular Stent Graft Device For Treatment Of Thoracic Aortic Aneurysms And Dissections - Us Fda Approved ?Device Should Be With Proximal Barbs, With Or Without Distal Bare Spring Configuration, And Should Be Tapered Or Non – Tapered. ?The Aortic Device Should Be Available In Any One Or More Of The Following Sizes: Od 26-44Mm; Length 4-24 Cm. The Device Should Be Able To Be Advanced On Up To 24 Fr Shaft Size. The Manufacturer Should Agree To Supply The Size Customized To The Patient’S Anatomy Based On Ct Angiography , Endovascular Stent Graft Device For Treatment Of Thoracic Aortic Aneurysms And Dissections – Ce/Dcgi Approved ?Device Should Be With Proximal Barbs, With Or Without Distal Bare Spring Configuration, And Should Be Tapered Or Non – Tapered. ?The Aortic Device Should Be Available In Any One Or More Of The Following Sizes: Od 26-44Mm; Length 4-24 Cm. The Device Should Be Able To Be Advanced On Up To 24 Fr Shaft Size. The Manufacturer Should Agree To Supply The Size Customized To The Patient’S Anatomy Based On Ct Angiography , Endovascular Stent Graft Device For Treatment Of Abdominal Aortic Aneurysms – Usfda Approved ?Device Should Be With Proximal Barbs, With Or Without Distal Bare Spring Configuration, And Should Be Either Tapered Or Non – Tapered ?Devices With Trans-Renal Or Suprarenal Fixation Should Be Quoted. ?The Aortic Device Should Be Available In Any 1 Or More Of The Following Sizes: Od 12-44Mm; Length 4-24 Cm. The Device Should Be Able To Be Advanced On Up To 24 Fr Shaft Size. ?The Limb Extensions Of The Main Device For Abdominal Aortic Applications Should Be Available In 12-22 Mm Diameter, With Or Without Flared Ends And Up To 12 Cm In Length The Manufacturer Should Agree To Supply The Size Customized To The Patient’S Anatomy Based On Ct Angiography , Endovascular Stent Graft Device For Treatment Of Abdominal Aortic Aneurysms – Ce/Dcgi Approved ?Device Should Be With Proximal Barbs, With Or Without Distal Bare Spring Configuration, And Should Be Either Tapered Or Non – Tapered ?Devices With Trans-Renal Or Suprarenal Fixation Should Be Quoted. ?The Aortic Device Should Be Available In Any 1 Or More Of The Following Sizes: Od 12-44Mm; Length 4-24 Cm. The Device Should Be Able To Be Advanced On Up To 24 Fr Shaft Size. ?The Limb Extensions Of The Main Device For Abdominal Aortic Applications Should Be Available In 12-22 Mm Diameter, With Or Without Flared Ends And Up To 12 Cm In Length The Manufacturer Should Agree To Supply The Size Customized To The Patient’S Anatomy Based On Ct Angiography , Renal Denervation Device For Rf Ablation Of Renal – Ce / Us Fda Approved , Renal Denervation Device For Rf Ablation Of Renal –Dcgiapproved , C.P. Stent Covered – Ce Approved Should Be Balloon Mounted. , C.P. Stent Covered – Us Fda Approved , C.P. Stent Covered – Dcgiapproved , Amplatzer Plug – Ce Approved , Amplatzer Plug – Us Fda Approved , Amplatzer Plug – Dcgiapproved , Snare For Periferal Use – Us Fda/Ceapproved , Snare For Periferal Use – Dcgiapproved , Long Artrial Sheeth 6F/7F/8F Length >=90 Cm – Braided –Us Fda/ Ce Approved , Long Artrial Sheeth 6F/7F/8F Length >=90 Cm – Braided – Dcgiapproved , Long Artrial Sheeth 6F/7F/8F Length >=90 Cm – Un Braided– Us Fda/ Ce Approved , Long Artrial Sheeth 6F/7F/8F Length >=90 Cm – Un Braided– Dcgiapproved , Long Artrial Sheeth Upto 90 Cm - Braided – Us Fda/ Ce Approved , Long Artrial Sheeth Upto 90 Cm - Braided – Dcgiapproved , Long Artrial Sheeth Upto 90 Cm - Unbraided – Us Fda/ Ce Approved , Long Artrial Sheeth Upto 90 Cm - Unbraided – Dcgiapproved , Cross – Over Sheeth - Braided – Us Fda/ Ce Approved , Cross – Over Sheeth - Braided – Dcgiapproved , Cross – Over Sheeth - Unbraided – Us Fda/ Ce Approved , Cross – Over Sheeth - Unbraided – Dcgiapproved , Visceral Type Catheter – Us Fda/ Ce Approved , Visceral Type Catheter – Dcgiapproved , Head Hunter Type Catheter – Us Fda/ Ce Approved , Head Hunter Type Catheter – Dcgiapproved , Vtk Type Catheter – Us Fda/ Ce Approved , Vtk Type Catheter – Dcgi Approved , Simmons Type Catheter – Us Fda/ Ce Approved , Simmons Type Catheter – Dcgiapproved , Cobra Type Catheter – Us Fda/ Ce Approved , Abdominal Stent Graft For Treating Aortic Aneurysm– Us Fda Approved , Abdominal Stent Graft For Treating Aortic Aneurysm– Ce Approved , Abdominal Stent Graft For Treating Aortic Aneurysm– Dcgi Approved , Thorosic Stent Graft For Treating Thorasic Aneurysm And Thorosic Dissection – Us Fda Approved , Thorosic Stent Graft For Treating Thorosic Aneurysm And Thorosic Dissection– Ce Approved , Thorosic Stent Graft For Treating Thorosic Aneurysm And Thorosic Dissection– Dcgi Approved , Covered Aortic Stent Balloon Mounted - Us Fda Approved , Covered Aortic Stent Balloon Mounted – Ce Approved , Covered Aortic Stent Balloon Mounted (Andra Stent Type) – Dcgi Approved , Non-Covered Aortic Stent Balloon Mounted - Us Fda Approved , Non-Covered Aortic Stent Balloon Mounted – Ce Approved , Non-Covered Aortic Stent Balloon Mounted(Endra Stent Type)– Dcgi Approved , Asd Occluders, -Percutaneous Transcatheter Closure For Non-Surgical Closure Of Atrial Septal Defect. Device Should Be Self-Expandable Double Disc Made Up Of Soft Nitinol Wire Mesh That Is Shaped Into Two Flat Discs And A Waist Between. Polyester Fabric Sewn Into Each Disc And The Waist To Promote Occlusion And Tissue In Growth. The Matellic Material Should Be Intaglio Treated To Improve Biocompatibilty And Reduce Nickel (Ni) Leaching. Device Should Be Mr Conditional Upto 3Tesla Or Less. Device Should Be Backed By Strong Clinical Study With Proven Success Rate For Pediatrics And Adults. – Usfda Approved Sizes - 4Mm, 5Mm, 6Mm, 7Mm, 8Mm, 9Mm, 10Mm, 11Mm, 12Mm, 13Mm, 14Mm, 15Mm, 16Mm, 17Mm, 18Mm, 19Mm, 20Mm, 22Mm, 24Mm, 26Mm, 28Mm, 30Mm, 32Mm, 34Mm, 36Mm, 38Mm, And,40Mm , Asd - Multi Fenestrated (Cribriform) Occluders, Percutaneous Transcatheter Closure For Non-Surgical Closure Of Atrial Septal Defect. Device Should Be Self-Expandable Double Disc Made Up Of Soft Nitinol Wire Mesh That Is Shaped Into Two Flat Discs And A Very Thin Waist Of 3Mm. Device Should Have Matched Disc Diameters To Maximise The Coverage Of Multiple Fenestrations. Polyester Fabric Sewn Into Each Disc Promote Occlusion And Tissue In Growth. The Matellic Material Should Be Intaglio Treated To Improve Biocompatibilty And Reduce Nickel (Ni) Leaching. Device Should Be Mr Conditional Upto 3Tesla Or Less. Device Should Be Backed By Strong Clinical Study With Proven Success Rate For Pediatrics And Adults. Usfda Approved Sizes - 18Mm, 25Mm, 30Mm, 35Mm, And 40Mm , Pda Occluders, Percutaneous Transcatheter Closure For Non-Surgical Closure Of Patent Ductus Arteriosus. Device Should Be Self- Expandable Made Up Of Soft Nitinol Wire Mesh, Which Has Been Heated And Set To Expand Into T-Shape. Retention Skirt Design Should Provide Secure Positioning With The Ductus And Reduce Embolization. Polyester Fabric Sewn Into The Device To Promote Occlusion And Tissue In Growth. The Matellic Material Should Be Intaglio Treated To Improve Biocompatibilty And Reduce Nickel (Ni) Leaching. Device Should Be Mr Conditional Upto 3Tesla Or Less. Device Should Be Backed By Strong Clinical Study With Proven Success Rate For Pediatrics And Adults.Usfda Approved Sizes - 0405Mm, 0406Mm, 0608Mm, 0810Mm, 1012Mm, 1214Mm, And 1416Mm , Pda Occluder With Double Disc, Percutaneous Transcatheter Closure For Non-Surgical Closure Of Moderate Patent Ductus Arteriosus. Device Should Be Self-Expandable Made Up Of Soft Nitinol Compliant-Multilayered Mesh And Dual Articulating Discs That Provide High Conformability To Treat Maximum Types Of Pda. Device Should Have Symmetric Design That Offers Procedural Flexibility To Choose Antegrade Or Retrograde Approach. Device Should Have Fabric-Free Technology That Allows For Delivery Through Low-Profile Catheter While Maintaining High Rate Of Occlusion. The Matellic Material Should Be Intaglio Treated To Improve Biocompatibilty And Reduce Nickel (Ni) Leaching. Device Should Be Mr Conditional Upto 3Tesla Or Less. Device Should Be Backed By Strong Clinical Study With Proven Success Rate For Pediatrics And Adults. Usfda Approved Sizes - 0304Mm, 0306Mm, 0404Mm, 0406Mm, 0504Mm, 0506Mm, 0604Mm, And 0606Mm , Pda Occluder With Double Disc (For Neonates), Percutaneous Transcatheter Closure For Non-Surgical Closure Of Small Patent Ductus Arteriosus In Neonates While Minimizing Protrusion. Device Should Be Self-Expandable Made Up Of Soft Nitinol Compliant-Multilayered Mesh. Device Should Have Low-Profile Dual Articulating Discs That Provide High Conformability To Treat Maximum Types Of Small Pdas. Device Should Have Symmetric Design That Offers Procedural Flexibility To Choose Antegrade Or Retrograde Approach. Device Must Containt Tightly Woven, Single Layer Mesh Development To Minimize Residual Shunt After Placement. Device Should Be Preloaded On Delivery Cable And Comes With A Special Low-Profile Delivery Catheter Of 4Fr. The Matellic Material Should Be Intaglio Treated To Improve Biocompatibilty And Reduce Nickel (Ni) Leaching. Device Should Be Mr Conditional Upto 3Tesla Or Less. Device Should Be Backed By Strong Clinical Study With Proven Success Rate For Pediatrics And Adults.Usfda Approved Sizes - 0302Mm, 0304Mm, 0306Mm, 0402Mm, 0404Mm, 0406Mm, 0502Mm, 0504Mm, And, 0506Mm , Muscular Vsd Occluder, Is A Percutaenous Transcatheter Closure For Non-Surgical Closure Of A Ventricular Septal Defect. The Occluder Is Designed To Close Complex Muscular Vsds In Patients To Be At High Risk Of Surgical Repair. The Device Should Be Self-Expandable Symmetric Double Disc Made From A Soft Nitinol Mesh. The Device Waist Should Be Self-Centered And Fill The Defect. The Device Should Be Filled With Polyester Material That Promotes Occlusion And Tissue In Growth. The Waist Length Should Be 7Mm To Accomodate The Thickness Of Muscular Ventricular Septal Wall. Symmetric Design Should Allow Both Antegrade And Retrograde Approach. The Matellic Material Should Be Intaglio Treated To Improve Biocompatibilty And Reduce Nickel (Ni) Leaching. Device Should Be Mr Conditional Upto 3Tesla Or Less. Device Should Be Backed By Strong Clinical Study With Proven Success Rate For Pediatrics And Adults.Usfda Approved Sizes - 4Mm, 6Mm, 8Mm, 10Mm, 12Mm, 14Mm, 16Mm, And 18Mm , P.I. Muscular Vsd Occluder, Is A Percutaenous Transcatheter Closure For Non-Surgical Closure Of A Ventricular Septal Defect. The Occluder Is Designed To Close Complex Muscular Vsds In Patients To Be At High Risk Post Infarction Caused Due To Mi. The Device Should Be Self-Expandable Symmetric Double Disc Made From A Soft Nitinol Mesh. The Device Waist Should Be Self-Centered And Fill The Defect. The Device Should Be Filled With Polyester Material That Promotes Occlusion And Tissue In Growth. The Waist Length Should Be 10Mm To Accomodate The Thickness Of Apical Ventricular Septal Wall. Symmetric Design Should Allow Both Antegrade And Retrograde Approach. The Matellic Material Should Be Intaglio Treated To Improve Biocompatibilty And Reduce Nickel (Ni) Leaching. Device Should Be Mr Conditional Upto 3Tesla Or Less. Device Should Be Backed By Strong Clinical Study With Proven Success Rate For Pediatrics And Adults. Usfda Approved Sizes - 16Mm, 18Mm, 20Mm, 22Mm, And 24Mm , Membranous Vsd Occluder, Is A Percutaneous Transcatheter Closure For Non-Surgical Closure Of Peri-Membranous Ventricular Septal Defect. It Should Be Non-Concentric Design Allows For Placement That Avoida Interference With Aortic Or Av Valves. The Device Should Be Made Up Of Soft Nitinol Meshwith Interwoven Polyester To Promote Occlusion And Tissue In-Growth. The Device Should Be Delievered Using A Pusher Catheter From Venous Approach. The Matellic Material Should Be Intaglio Treated To Improve Biocompatibilty And Reduce Nickel (Ni) Leaching. Device Should Be Mr Conditional Upto 3Tesla Or Less. Device Should Be Backed By Strong Clinical Study With Proven Success Rate For Pediatrics And Adults.Usfda Approved Sizes - 4Mm, 5Mm, 6Mm, 7Mm, 8Mm, 9Mm, 10Mm, 11Mm, 12Mm, 13Mm, 14Mm, 15Mm, 16Mm, 17Mm, And 18Mm , Pfo Occluder, Is A Percutaneous Transcatheter Closure For Non-Surgical Closure Of Patent Foramen Ovale. Device Should Be Self- Expandable Double Disc Made Up Of Soft Nitinol Wire Mesh That Is Shaped Into Two Flat Discs And A Very Thin Waist Of 3Mm. Device Should Have Matched Disc Diameters To Maximise The Coverage Of Foramen Ovale. Polyester Fabric Sewn Into Each Disc Promote Occlusion And Tissue In Growth. The Matellic Material Should Be Intaglio Treated To Improve Biocompatibilty And Reduce Nickel (Ni) Leaching. Device Should Be Mr Conditional Upto 3Tesla Or Less. Device Should Be Backed By Strong Clinical Study With Proven Success Rate For Pediatrics And Adults. Usfda Approved Sizes - 18Mm, 25Mm, 30Mm, And 35Mm , Atv, Special Delivery System Designed For Asd And Pfo Cases. This Delivery System Comes With An Ultra-Flexible Tip For Better Positioning Of The Device. Enhanced Delivery Cable Improves The Assessment Of Device Final Position Prior To Cable Release. It Is Designed For No Compromise On Torque Strength, Sheath Diameter And Pushability.Usfda Approved Sizes - 6Fr, 7Fr, 8Fr, 9Fr, 10Fr, 12Fr, And 13Fr , Itv, Special Delivery System With Delivery Cable Angeled At 45°. Used For Asd And Pfo Cases Usfda Approved Sizes - 6Fr, 7Fr, 8Fr, 9Fr, 10Fr, 12Fr, And 13Fr , Itv, Special Delivery System With Delivery Cable Angeled At 180°. Used For Vsd And Pda Cases Usfda Approved Sizes - 5Fr, 6Fr, 7Fr, 8Fr, And 9Fr , Tvlp, Special Delivery System For Pda Occluder With Double Disc Angeled At 90° (Ado Ii) Usfda Approved Sizes - 4Fr And 5Fr , Tvlpc, Special Delivery Catheter For Speical Sizes Of Pda Occluder With Double Disc Angeled At 90° (Piccolo Device) Usfda Approved Sizes - 4Fr , Itvp, Special Delivery System With Pusher Catheter Angeled At 180°Usfdaapproved Sizes - 7Fr, 8Fr And 9Fr , Laa Closure, Is A Percutaneous Transcatheter Closure For Non-Surgical Closure Of Left Atrial Appendage. Having An Innovative Design Of Cylindrical Plug Attached With The Retention Skirt. Cylindrical Plug Shaped Head Is Designed To Trap Trabeculations. Device Should Be Preloaded On The Delivery Cable With Delivery Profile Of 12Fr To 14Fr. Devide Should Be Made Up Of Soft Woven Nitinol Mesh. The Matellic Material Should Be Intaglio Treated To Improve Biocompatibilty And Reduce Nickel (Ni) Leaching. Device Should Be Mr Conditional Upto 3Tesla Or Less. Device Should Be Backed By Strong Clinical Study With Proven Success Rate For Pediatrics And Adults. Usfda Approvedsizes - 16Mm, 18Mm, 20Mm, 22Mm, 25Mm, 28Mm, 31Mm, And, 34Mm , Tv, Special Delivery System With Dual Angeled Sheath At 45° X 45° With The Usable Length Of 80Cm Specially Designed For Laa Occludersusfda Approvedsize - 12Fr. And 14Fr. , Sizing Balloon With A Triple Lumen Balloon Catheter With Three Radiopaque Marker Bands Located Inside The Balloon To Allow For Radiographic Measurement. The Centre Of The Balloon Should Contains A Pair Of Marker Bands 0.4Mm Apart For Corrent Balloon Alignment While Measuing The Defect And One Marker Band 15Mm Proximal Of The Pair.Usfda Approvedsize - 18Mm, 24Mm. And 34Mm , Pvl Occluder Is A Percutaneour Transcatheter Closure Of Para Valvular Leak Which Is A Serious Complication Of Valve Replacement Surgery. Devide Should Be Made Up Of Soft Woven Muti-Layered Nitinol Mesh Designed To Increase Density And Provide Rapid Occlusion. Low Profile 4Fr To 7Fr Sheath To Facilitate Defect Crossing. Oblonged Shape To Improve Wall Apposition And Enhance Stability In Pvl. Device Orientation Should Be Defined Through A Small Platinum Marker On The Distal Rim. The Matellic Material Should Be Intaglio Treated To Improve Biocompatibilty And Reduce Nickel (Ni) Leaching. Device Should Be Mr Conditional Upto 3Tesla Or Less. Device Should Be Backed By Strong Clinical Study With Proven Success Rate For Pediatrics And Adults.Usfda Approved Size - 0204Mm, 0306Mm, 0408Mm, 0310Mm, 0510Mm, 0312Mm, 0512Mm, 0314Mm, And 0514Mm. , Pda Closure Devices Without Delivery System — Ce/Dcgi Approved Available In All The Sizes • Hat-Shaped Designed Pda Occluder Device • Platinum Coating Of =25 ? Using Nano Fusion Technology • Polypropylene Fabric Sewn Inside The Occluder Device • Extended Retention Portion Provides Proper Positioning Of The Device In The Ductus Arteriosus • Available Sizes- 4/6, 6/8, 8/10, 10/12, 12/14, 14/16, 16/18, 18/20Mm , Delivery Sheath For Pda Closure Device — Ce /Dcgi Approved , Pda Closure Devices With Delivery System – Ce Approved/ Dgci Approved ·Available In All The Sizes• Hat-Shaped Designed Pda Occluder Device • Platinum Coating Of =25 ? Using Nano Fusion Technology • Polypropylene Fabric Sewn Inside The Occluder Device • Extended Retention Portion Provides Proper Positioning Of The Device In The Ductus Arteriosus • Available Sizes- 4/6, 6/8, 8/10, 10/12, 12/14, 14/16, 16/18, 18/20Mm , Vsd Closure Devices Without Delivery System — Ce/Dcgi Approved• Self-Expanding, Self-Centering Double-Disc Device • Platinum Coating Of =25 ? Using Nano Fusion Technology • Polypropylene Fabric Sewn Inside The Occluder Device • Available Sizes- 4-4, 4-10, 6-4, 6-10, 8-4, 8-10, 10-4, 10-10, 12-4, 12-10Mm • Certificates- Ce & Dcgi Approved • Shelf Life- 3 Years , Delivery Sheath For Vsd Closure Device — Ce Approved , Vsd Closure Devices With Delivery System — Ce/Dcgi Approved• Self-Expanding, Self-Centering Double-Disc Device • Platinum Coating Of =25 ? Using Nano Fusion Technology • Polypropylene Fabric Sewn Inside The Occluder Device • Available Sizes- 4-4, 4-10, 6-4, 6-10, 8-4, 8-10, 10-4, 10-10, 12-4, 12-10Mm • Delivery Cable Available Along With Cable Sheath In Individual Packaging • Soft And Flexible Distal End Of Delivery Cable To Navigate In Various Anatomies • Availability Of ‘S-Shaped’ Sheath • Certificates- Ce & Dcgi Approved • Shelf Life- 3 Years , Valve • Self-Expanding Frame, Supra-Annular Valve Design, Bovine Pericardial Valve • Proprietary Anti-Calcification Tissue Treatment • Extended Internal Sealing Skirt • Two Rows Of Radio-Opaque Markers On The Frame • Varying Radial Force Frame – Optimal Forces At All 3 Parts Of The Frame • Available In Three Sizes Of 22, 26, And 30 Mm, Which Cover The Treatable Annular Diameter Range From 17 To 27 Mm • Post Dilatation Limits Of Valve Frame Equal To Approved Annulus Diameter Limit • Cell Size Of = 15 French • Less Metal At The Inflow Section • Certificates- Ce & Dcgi Approved , Pfo Closure Devices With Delivery System — Ce/Dcgi Approved• Self-Expanding, Self-Centering Double-Disc Occluder • Platinum Coating Of =25 ? Using Nano Fusion Technology • Polypropylene Fabric Sewn Inside The Occluder Device • Available In 6 Sizes, 5 Sizes (18/18, 25/18, 25/25, 30/25, 30/30 Mm) Which Are 8F Compatible And 1 Size (35/25 Mm) Which Is 9F Compatible • 6F Delivery Cable Available In Individual Packaging • Certificates- Ce & Dcgi Approved • Shelf Life- 3 Years , Pfo Closure Devices Without Delivery System — Ce/Dcgi Approved• Self-Expanding, Self-Centering Double-Disc Occluder • Platinum Coating Of =25 ? Using Nano Fusion Technology • Polypropylene Fabric Sewn Inside The Occluder Device • Available In 6 Sizes, 5 Sizes (18/18, 25/18, 25/25, 30/25, 30/30 Mm) Which Are 8F Compatible And 1 Size (35/25 Mm) Which Is 9F Compatible • Certificates- Ce & Dcgi Approved • Shelf Life- 3 Years , Delivery Sheath For Pfo Closure Device — Ce/Dcgi Approved •Compatible With The Device Approved , Asd Closure Devices Without Delivery System– Ce Approved/Dcgi Approved ·Approved For Pediatric/Adult Use • Self-Expanding, Self-Centering Double-Disc Device • Platinum Coating Of =25 ? Using Nano Fusion Technology • Polypropylene Fabric Sewn Inside The Occluder Device • Available In Sizes- 8, 10, 12, 14, 16, 18, 20, 22, 24, 26, 28, 30, 32, 34, 36, 38 & 40Mm , Asd Closure Devices With Delivery System – Ce Approved/Dcgi Approved ·Approved For Pediatric/Adult Use ·Self-Centering, Detachable Device With Delivery Cable • Self-Expanding, Self-Centering Double-Disc Device • Platinum Coating Of =25 ? Using Nano Fusion Technology • Polypropylene Fabric Sewn Inside The Occluder Device • Available In Sizes- 8, 10, 12, 14, 16, 18, 20, 22, 24, 26, 28, 30, 32, 34, 36, 38 & 40Mm And Delivery Sheath , Delivery Sheath For Asd Closure Device - Ce/Dcgi Approved , Delivery Cable For Asd/Vsd/Pda/Pfo Devices - Ce/Dcgi Approved , Left Atrial Appendage Closure Device Us Fda Approved , Occlusion Balloon-Dcgi With Us Fda / Ce Approved ?Shouldbe Soft Compliant Balloon Material With Radio-Opaque Markers At Both Distal And Proximal End Of Balloon ?Should Be 14Fr / 16Fr Sheath And 0.035”/0.038” Wire Compatible. Should Be Available In Diameter 20 Mm/ 27 Mm / 33 Mm And 40 Mm. , Pda Coils Made Of Steel/ Nitinol/Platinum - Us Fda Approved ? 0.035, 0.038 Inches Sizes Ranging From 2 X 2 To 15 X 15 , Pda Coils Made Of Steel/ Nitinol/Platinum - Ce Approved ? 0.035, 0.038 Inches Sizes Ranging From 2 X 2 To 15 X 15 , Pda Coils Made Of Steel/ Nitinol/Platinum – Dcgi Approved ? 0.035, 0.038 Inches Sizes Ranging From 2 X 2 To 15 X 15 , 0.052 Inch Pda Coils Made Of Steel/ Nitinol/Platinum - Us Fda Approved Sizes Ranging From 2 X 2 To 15 X 15 , 0.052 Inch Pda Coils Made Of Steel/ Nitinol/Platinum - Ce Approved Sizes Ranging From 2 X 2 To 15 X 15 , 0.052 Inch Pda Coils Made Of Steel/ Nitinol/Platinum – Dcgi Approved Sizes Ranging From 2 X 2 To 15 X 15 , Embolisation Coils (0.018 Inch) - Us Fda Approved Sizes Ranging From 2 X 2 To 15 X 15 , Embolisation Coils (0.018 Inch) - Ce Approved Sizes Ranging From 2 X 2 To 15 X 15 , Embolisation Coils (0.018 Inch) – Dcgi Approved Sizes Ranging From 2 X 2 To 15 X 15 , Embolisation Coils (0.035 Inch) - Us Fda Approved Sizes Ranging From 2 X 2 To 15 X 15 , Embolisation Coils (0.035 Inch) - Ce Approved Sizes Ranging From 2 X 2 To 15 X 15 , Embolisation Coils (0.035 Inch) – Dcgi Approved Sizes Ranging From 2 X 2 To 15 X 15 , Embolisation Coils (0.052 Inch) - Us Fda Approved Sizes Ranging From 2 X 2 To 15 X 15 , Embolisation Coils (0.052 Inch) - Ce Approved Sizes Ranging From 2 X 2 To 15 X 15 , Embolisation Coils (0.052 Inch) –Dcgi Approved Sizes Ranging From 2 X 2 To 15 X 15 , Park Blade Septectomy Catheter - Us Fda Approved , Park Blade Septectomy Catheter - Ce Approved , Park Blade Septectomy Catheter – Dcgi Approved , Embolisation Coils - Us Fda Approved ?Should Be 0.014/0.018” Compatible ?Should Be Made Of Platinum With Synthetic Fibres ?Should Be Non Tapering/Straight ?Should Be Mr Compatible ?Should Be Available In Any Or The Following Diameters: 2-10 Mm Should Be Of Various Lengths; The Length Of The Coil At Each Diameter Should Be Stated , Embolisation Coils - Ce Approved ?Should Be 0.014/0.018” Compatible ?Should Be Made Of Platinum With Synthetic Fibres ?Should Be Non Tapering/Straight ?Should Be Mr Compatible ?Should Be Available In Any Or The Following Diameters: 2-10 Mm Should Be Of Various Lengths; The Length Of The Coil At Each Diameter Should Be Stated , Embolisation Coils – Dcgi Approved ?Should Be 0.014/0.018” Compatible ?Should Be Made Of Platinum With Synthetic Fibres ?Should Be Non Tapering/Straight ?Should Be Mr Compatible ?Should Be Available In Any Or The Following Diameters: 2-10 Mm Should Be Of Various Lengths; The Length Of The Coil At Each Diameter Should Be Stated , Embolisation Coils - Usfda Approved ?Should Be 0.035/0.038” Compatible ?Should Be Made Of Platinum With Synthetic Fibres ?Should Be Mr Compatible ?Should Be Tapering From A Larger To A Smaller End ?Should Be Available In Following Sizes: Diameters: 5-10 Mm And Length 2-15 Cm The Diameter To Tapered End For Tapering Type Coil Should Be Mentioned , Embolisation Coils - Ce Approved ?Should Be 0.035/0.038” Compatible ?Should Be Made Of Platinum With Synthetic Fibres ?Should Be Mr Compatible ?Should Be Tapering From A Larger To A Smaller End ?Should Be Available In Following Sizes: Diameters: 5-10 Mm And Length 2-15 Cm The Diameter To Tapered End For Tapering Type Coil Should Be Mentioned , Embolisation Coils – Dcgi Approved ?Should Be 0.035/0.038” Compatible ?Should Be Made Of Platinum With Synthetic Fibres ?Should Be Mr Compatible ?Should Be Tapering From A Larger To A Smaller End ?Should Be Available In Following Sizes: Diameters: 5-10 Mm And Length 2-15 Cm The Diameter To Tapered End For Tapering Type Coil Should Be Mentioned , Embolisation Coils - Us Fda Approved ? Should Be 0.035/0.038/0.052” Compatible ? Should Be Non Tapering/Straight ? Should Be Made Of Stainless Steel With Synthetic Fibres Should Be Available In The Following Sizes: Diameters: 3-15 Mm And Length 2-15 Cm , Embolisation Coils - Ce Approved ? Should Be 0.035/0.038/0.052” Compatible ? Should Be Non Tapering/Straight ? Should Be Made Of Stainless Steel With Synthetic Fibres Should Be Available In The Following Sizes: Diameters: 3-15 Mm And Length 2-15 Cm , Embolisation Coils – Dcgi Approved ? Should Be 0.035/0.038/0.052” Compatible ? Should Be Non Tapering/Straight ? Should Be Made Of Stainless Steel With Synthetic Fibres Should Be Available In The Following Sizes: Diameters: 3-15 Mm And Length 2-15 Cm , Coil Pusher Wire For 0.014/0.018” Coils, Compatible With The Quoted Micro Catheters - Us Fda Approved , Coil Pusher Wire For 0.014/0.018” Coils, Compatible With The Quoted Micro Catheters - Ce Approved , Coil Pusher Wire For 0.014/0.018” Coils, Compatible With The Quoted Microcatheters – Dcgi Approved , Gelfoam Sheet For Vascular Embollization - Us Fda Approved , Gelfoam Sheet For Vascular Embollization - Ce Approved , Gelfoam Sheet For Vascular Embollization – Dcgi Approved , Liquid Embolization System Available In Various Sizes (2Ml, 3Ml & 6Ml)– Us Fda/ Ce / Dcgi Approved , Pbmv Balloon (All Types And Sizes) With Accessories – Us Fda Approved , Pbmv Balloon (All Types And Sizes) With Accessories – Ce Approved , Pbmv Balloon (All Types And Sizes) With Accessories – Dcgi Approved , Pbmv Balloon (All Types And Sizes) Without Accessories – Us Fda Approved , Pbmv Balloon (All Types And Sizes) Without Accessories –Ce Approved , Pbmv Balloon (All Types And Sizes) Without Accessories –Dcgi Approved , Accessories Only For The Above Pbmv Balloons – Us Fda Approved , Accessories Only For The Above Pbmv Balloons – Ce Approved , Accessories Only For The Above Pbmv Balloons – Dcgi Approved , Pbmv Balloon With Side Safety / Microholes With Accessories– Us Fda Approved , Pbmv Balloon With Side Safety / Microholes With Accessories– Ce Approved , Pbmv Balloon With Side Safety / Microholes With Accessories– Dcgiapproved , Pbmv Balloon With Side Safety / Microholes Without Accessories – Us Fda Approved , Pbmv Balloon With Side Safety/ Microholes Without Accessories– Ce Approved , Pbmv Balloon With Side Safety/ Microholes Without Accessories– Dcgiapproved , Ptmc Balloon With Hole In Balloon – Us Fda Approved , Ptmc Balloon With Hole In Balloon – Ce Approved , Ptmc Balloon With Hole In Balloon – Dcgi Approved , Ptmc Balloon (With Hole In Balloon) With All Acessories- Us Fda Approved , Ptmc Balloon (With Hole In Balloon) With All Acessories- Ce Approved , Ptmc Balloon (With Hole In Balloon) With All Acessories- Dcgi Approved , Tavi (|Trans Catheter Aortic Valve Replacement System With All Required Accessories) - – Dcgi With Us Fda /Ce Approved , Tavi (|Trans Catheter Aortic Valve Replacement System With All Required Accessories)- Ce Approved , Tavi (|Trans Catheter Aortic Valve Replacement System With All Required Accessories) – Dcgi Approved , Self Expandable Trans Catheter Aortic Valve Replacement System With All Required Accessories –Us Fda /Ce Approved ?Should Be Inall Sizes Diameter Anti – Calcification And Chemical Dehydration Thin & Strong Low Profile With Delivery System. , Self Expandable Trans Catheter Aortic Valve Replacement System With All Required Accessories – Dcgi Approved ?Should Be Inall Sizes Diameter Anti – Calcification And Chemical Dehydration Thin & Strong Low Profile With Delivery System. , Self Expandable Trans Catheter Tricuspidvalve Replacement System With All Required Accessories – Dcgi With Us Fda /Ce Approved ?Should Be Inall Sizes Diameter Anti – Calcification And Chemical Dehydration Thin & Strong Low Profile With Delivery System. , Trans Catheter Tricuspid Valve Replacement System With All Required Accessories – Dcgi With Us Fda /Ce Approved ?Should Be Inall Sizes Diameter Anti – Calcification And Chemical Dehydration Thin & Strong Low Profile With Delivery System. , Mitra-Clip (Trans Catheter Mitral Valve Clip System) - Dcgi With Us Fda / Ce Approved , Mitra-Valve (Trans Catheter Mitral Valve) - Dcgi , Tavi (|Trans Catheter Aortic Valve Replacement System With All Required Accessories)- Usfda Approved , Tavi (|Trans Catheter Aortic Valve Replacement System With All Required Accessories)- Ce Approved , Tavi (|Trans Catheter Aortic Valve Replacement System With All Required Accessories)- Dcgi Approved , Tavi Guide-Wire -Dcgi With Us Fda / Ce Approved ?Should Be Available In Diameter 0.035, Length 250-275 Cm, Should Have Spring Coil Ptfe Coating And Extra Small, Small & Large Curves. , Wire 0.018” Regular Length, Regular Shaft Stiffness - Us Fda Approved Floppy Tip, Straight / J Shaped Tip, 140-300Cm Long , Wire 0.018” Regular Length, Regular Shaft Stiffness - Ce Approved Floppy Tip, Straight / J Shaped Tip, 140-300Cm Long , Wire 0.018” Regular Length, Regular Shaft Stiffness – Dcgi Approved Floppy Tip, Straight / J Shaped Tip, 140-300Cm Long , Wire 0.018” Regular Length, Extra – Stiff Shaft - Us Fda Approved Floppy Tip, Straight / J Shaped Tip, 140-300Cm Long , Wire 0.018” Regular Length, Extra – Stiff Shaft- Ce Approved Floppy Tip, Straight / J Shaped Tip, 140-300Cm Long , Wire 0.018” Regular Length, Extra – Stiff Shaft- Dcgi Approved Floppy Tip, Straight / J Shaped Tip, 140-300Cm Long , Valvoplasty Balloon Catheters - Us Fda Approved ?Varying Sizes And Diameters Approved For Pediatric/Adults Use , Valvoplasty Balloon Catheters - Ce Approved ?Varying Sizes And Diameters Approved For Pediatric/Adults Use , Valvoplasty Balloon Catheters – Dcgi Approved ?Varying Sizes And Diameters Approved For Pediatric/Adults Use , Special Balloon Catheter Compatible With 4 French Sheath - Us Fda Approved ?Compatible With 0.018 Inch Guide Wire Varying Length And Diamete , Special Balloon Catheter Compatible With 4 French Sheath - Ce Approved ?Compatible With 0.018 Inch Guide Wire Varying Length And Diameter , Special Balloon Catheter Compatible With 4 French Sheath – Dcgi Approved ?Compatible With 0.018 Inch Guide Wire Varying Length And Diameter , Special Pediatric Valvoplasty Balloon Catheters Compatible With 4 French Sheath - Us Fda Approved ?Compatible With 0.025 Inch Guide Wire Varying Length And Diameter , Special Pediatric Valvoplasty Balloon Catheters Compatible With 4 French Sheath - Ce Approved ?Compatible With 0.025 Inch Guide Wire Varying Length And Diameter , Special Pediatric Valvoplasty Balloon Catheters Compatible With 4 French Sheath – Dcgi Approved ?Compatible With 0.025 Inch Guide Wire Varying Length And Diameter , Valvoplasty Balloon Catheters (Sizes 10 – 22 Mm)- Us Fda Approved ?Approved For Pediatric/Adults Use ?Varying Length And Diameter Nominal Pressure < 4 Atm , Valvoplasty Balloon Catheters (Sizes 10 – 22 Mm)- Ce Approved ?Approved For Pediatric/Adults Use ?Varying Length And Diameter Nominal Pressure < 4 Atm , Valvoplasty Balloon Catheters (Sizes 10 – 22 Mm)- Dcgi Approved ?Approved For Pediatric/Adults Use ?Varying Length And Diameter Nominal Pressure < 4 Atm , Balloon Catheters (Sizes 10 – 22 Mm)- Us Fda Approved ?Approved For Pediatric/Adults Use ?Varying Length And Diameter Nominal Pressure < 8 Atm , Balloon Catheters (Sizes 10 – 22 Mm)- Ce Approved ?Approved For Pediatric/Adults Use ?Varying Length And Diameter Nominal Pressure < 8 Atm , Balloon Catheters (Sizes 10 – 22 Mm)- Dcgiapproved ?Approved For Pediatric/Adults Use ?Varying Length And Diameter Nominal Pressure < 8 Atm , Balloon In Balloon Catheters- Us Fda Approved Quote In All Sizes , Balloon In Balloon Catheters- Ce Approved Quote In All Sizes , Balloon In Balloon Catheters- Dcgiapproved Quote In All Sizes , Fogarty Embolectomy Catheter - Us Fda Approved ?4Fr./5Fr./6 Fr. Sizes Metal Rod At Tip Of The Catheter To Enable Angulations Up To 60 Degrees , Fogarty Embolectomy Catheter - Ce Approved ?4Fr./5Fr./6 Fr. Sizes Metal Rod At Tip Of The Catheter To Enable Angulations Up To 60 Degrees , Fogarty Embolectomy Catheter - Dcgi Approved ?4Fr./5Fr./6 Fr. Sizes Metal Rod At Tip Of The Catheter To Enable Angulations Up To 60 Degrees , Atrial Septostomy Catheter - Us Fda Approved 4Fr./5Fr./6 Fr. Sizes , Atrial Septostomy Catheter - Ce Approved 4Fr./5Fr./6 Fr. Sizes , Atrial Septostomy Catheter – Dcgi Approved 4Fr./5Fr./6 Fr. Sizes , Detachable Balloon - Us Fda Approved , Detachable Balloon - Ce Approved , Detachable Balloon – Dcgi Approved , Vascular Plugs – Us Fda Approved , Vascular Plugs – Ce Approved , Vascular Plugs Implantation– Dcgi With Us Fda / Ce Approved ?Should Be Titanium Nitride Coated. ?Should Have Ptfe Layers For Enhanced Occlusion. Should Be Available In Various Sizes (4.0- 24.0 Mm. , Valvoplasty Balloon Catheters Tyshek Type (All Sizes) - Us Fda Approved ?Approved For Pediatric/Adults Use ?Varying Length And Diameter Nominal Pressure < 4 Atm , Valvoplasty Balloon Catheters Tyshek Type (All Sizes)- Ce Approved ?Approved For Pediatric/Adults Use ?Varying Length And Diameter Nominal Pressure < 4 Atm , Aortic Stent Graft Abdominal -Dcgi With Us Fda / Ce Approved ?Endovascular Stent Graft Device For The Treatment Of Thoracic Aortic Aneurysm Or Dissection With Ptfe Dual Membrane Coating. With Metal Spine On The Greater Curvature To Avoid Stent Shortening And Provide Axial Support. , A U I Stent Graft Systemdcgi With Us Fda / Ce Approved ?Specifically Designed For Treatment Of Endovascular Abdominal Aortic Aneurysm A Self – Expandable Nitinol Stent With Ptfe Dual Membrane Coating & Offers Axial Support Preventing Foreshortening Of Stent. , Iliac Stent Graft -Dcgi With Us Fda / Ce Approved ?Endo-Vascular Stent Graft Device For The Treatment Iliac Aneurysm Or Dissection. With Proximal Bare Spring Configuration. It Should Be An Extension To Aaa Graft System , Multifunctional Occluder-Dcgi With Us Fda / Ce Approved ?For Occlusion Of Muscular Vsd Peri-Membranous Vsd, Rsov, Apex Window & Av Fistula Should Be Low Profile (4F-6F) And Should Come With A Elongatable Waist. , Peripheral Snare With Tungsten Loop Coated With Titanium Nitride - Dcgi With Ce/ Us Fda Approved Loop Size 5Mm To 35Mm. Shaft Size Up To 6F , Peripheral Snare With Tungsten Loop Coated With Titanium Nitride (5Mm To 35Mm) -Dcgi With Us Fda / Ce Approved , Ivc Filter For Optimal Filtration Of Ivc Up To 23Mm -Dcgi With Us Fda / Ce Approved ?Made Of National And Filter Length Up To 40 ?For Temporary Placement It Should Be Administrable From Jugular/ Femoral Route , Coronary Snare With Tungsten Loop Coated With Titanium Nitride (4Mm&7Mm) -Dcgi With Us Fda / Ce Approved , Steerable Sheath With Deflectable Tip (190-160Degree) -Dcgi With Us Fda / Ce Approved , Pva Particles With Consistent Sized Particles - Dcgi With Us Fda/ Ce Approved , Endomyocardial Biopsy (Emb) Forceps Set - Us Fda Approved Set Should Include ?Should Include An Endomyo-Cardial Biopsy Foreeps And Compatible Pre-Shaped Introducer Sheath With Side Arm And Its Dilator , Endomyocardial Biopsy (Emb) Forceps Set – Ce/Dcgi Approved Set Should Include ?Should Include An Endomyo-Cardial Biopsy Foreeps And Compatible Pre-Shaped Introducer Sheath With Side Arm And Its Dilator ?Variable Lengths And Sizes Should Be Available For Both For Jugular And Femoral Access , Intravascular Retriever – Snare (‘Amplatz Gooseneck’ Type) - Us Fda Approved Snare Kit Should Include ?A Snare And Its Compatible Sheath ?Should Have Nitinol Shaft ?Should Have 90 Degree Preformed Snare Loop Variable Sizes Of Loop (5-35 Mm) , Intravascular Retriever – Snare (‘Amplatz Gooseneck’ Type) - Ce Approved Snare Kit Should Include ?A Snare And Its Compatible Sheath ?Should Have Nitinol Shaft ?Should Have 90 Degree Preformed Snare Loop Variable Sizes Of Loop (5-35 Mm) , Intravascular Retriever – Snare (‘Amplatz Gooseneck’ Type) –Dcgiapproved Snare Kit Should Include ?A Snare And Its Compatible Sheath ?Should Have Nitinol Shaft ?Should Have 90 Degree Preformed Snare Loop Variable Sizes Of Loop (5-35 Mm) , Sheaths For Intravascular Snares - Us Fda Approved Should Be Compatible With Item No. 3 &4 , Sheaths For Intravascular Snares - Ce Approved Should Be Compatible With Item No. 3 & 4 , Sheaths For Intravascular Snares – Dcgi Approved Should Be Compatible With Item No. 3 & 4 , Intravascular Retriever – Microsnare (‘ Amplatz Gooseneck’ Type) - Us Fda Approved Microsnare Kit Should Include ?A Microsnare, Compatible Micro – Catheter, Micro – Catheter Introducer And A Torque Device ?Should Have Nitinol Shaft ?Should Have 90 Degree Preformed Snare Loop Variable Sizes (2-7 Mm) , Intravascular Retriever – Microsnare (‘ Amplatz Gooseneck’ Type) - Ce Approved Microsnare Kit Should Include ?A Microsnare, Compatible Micro – Catheter, Micro – Catheter Introducer And A Torque Device ?Should Have Nitinol Shaft ?Should Have 90 Degree Preformed Snare Loop Variable Sizes (2-7 Mm) , Intravascular Retriever – Microsnare (‘ Amplatz Gooseneck’ Type) – Dcgiapproved Microsnare Kit Should Include ?A Microsnare, Compatible Micro – Catheter, Micro – Catheter Introducer And A Torque Device ?Should Have Nitinol Shaft ?Should Have 90 Degree Preformed Snare Loop Variable Sizes (2-7 Mm) , Accessories For Intravascular Microsnare - Us Fda Approved Should Be Compatible With Item No. 7 & 8 , Accessories For Intravascular Microsnare - Ce Approved Should Be Compatible With Item No. 7 & 8 , Accessories For Intravascular Microsnare – Dcgiapproved Should Be Compatible With Item No. 7 & 8 , Intravascular Retriever – Basket - Us Fda Approved Set Should Include ?Basket Retriever And Its Catheter Should Be Available In All Sizes , Intravascular Retriever – Basket - Ce Approved Set Should Include ?Basket Retriever And Its Catheter Should Be Available In All Sizes , Intravascular Retriever – Basket – Dcgi Approved Set Should Include ?Basket Retriever And Its Catheter Should Be Available In All Sizes , Intravascular Retriever Snare Kit Goose Neck Type – Dcgi & Us Fda / Ce Approved , Sizing Balloon For Device Closure — Circular Shape - Ce Approved , Sizing Balloon For Device Closure - Round Shape - Dcgi /Ce Approved , Cobalt Cliromium Renal Stents, Premounted On Balloon Dcgi Approved · Monorail (Rapid Exchange) And Over-The-Wire (Otw) · Available In The Sizes And Lengthsthree Mid-Strut To Mid-Strut Connectors Between Two Rings. • Two Different Crown Design For Diameters Between 5- 7 Mm. • Crossing Profile = 1.50 Mm • Zero Foreshortening • Available In 5,6 And 7Mm Diameters With Length Of 12,15 And 18 Mm. , Permanent Venacava Filter– Ce Approved , Permanent Venacava Filter– Us Fda Approved , Permanent Venacava Filter– Dcgi Approved , Temporary Venacava Filter– Ce Approved , Temporary Venacava Filter– Us Fda Approved , Temporary Venacava Filter– Dcgi Approved , 1 Port Cath-Lock™ Introducer Sheath With Hemostasis Valve And Sideport, Dilator,And 50 Cm Double Distal Guidewire With “J” And Straight Ends , 2 Port Hemostasis Adapter With Sideports And Cath-Lock™ Sealing Mechanism, Venous Sheath,Dilator And 50 Cm Double Distal Guidewire With “J” And Straight Ends , 3 Port Hemostasis Adapter With Sideports And Cath-Lock™ Sealing Mechanism, Venous Sheath,Dilator And 50 Cm Double Distal Guidewire With “J” And Straight Ends , Introducer Sheath With Hemostasis Valve And Sideport, And Dilator , Mullins Style Curve 6/7/8 F Size, 61Cm Usable Length , 67Cm Dilator Usable Length , Swartz Lntroducer Braided Sheath With Hemostatic Valve Sl0/Sl1/Sl2/Sl3 (8F, 63 Cm Usable Length And 67Cm Dilator Usable Length) Accomodates Maximum 0.32 Guidewire , Swartz Lntroducer Non Braided Sheath With Hemostatic Valve Sr0/Sr1/Sr2/Sr3 (8F, 63 Cm),(8F, 63 Cm Usable Length) Accomodates Maximum 0.38 Guidewire , 8.5 F : 71 Cm Bi-Directional (Assymetrical ) Deflectable Sheath , Curl Dimension 16.8Mm And 22.4 Mm With Integrated Hemostasis Valve And Radiopaque Tip Marker And Various Curve Options , Compatible With 98 Cm Transseptal Needle Along With 180 Cm Super Stiff Guidewire , 8.5 F : 40 Cm Bi-Directional (Assymetrical ) Deflectablesheath Used For Epicardialwith Integrated Hemostasis Valve And Radiopaque Tip Marker And Various Curve Options , Brk/Brk-1Needle-Adult, 18 Gauge, Usable Length 71 Cm. , Brk/Brk-1 Needle-Adult, 18 Gauge, Usable Length 98 Cm. , Fixed Curve Quadripolar Electrophysiology Catheter (6F/5F/4F, 1Mm Band Electrode) Crd/Jsn/Dao, 2-5-2 Mm Electrode Spacing , Fixed Curve Quadripolar Electrophysiology Catheter (6F) Crd-2, 5Mmelectrode Spacing , Fixed Cuve (Csl) Decapolar Catheter (6F) -65 Cm Usable Length With 5-5-5 Spacing With Tip Electrode 2Mm , Fixed Cuve (Csl) Decapolar Catheter (6F) -120 Cm Usable Length With 5-5-5 Spacing With Tip Electrode 2Mm , Deflectable Decapolar Electrophysiology Catheter With Connector (6F)-110Cm Usable Length With 2-5-2 Spacing , Deflectable Decapolar Electrophysiology Catheter With Connector (5F)-110Cm Usable Length With 2-5-2 Spacing , Deflectable Decapolar Electrophysiology Catheter With Connector (4F)-110Cm Usable Length With 2-5-2 Spacing , Duodecapolar Electrophysiology Catheter-20 Poles (7F) Usable Length 95Cm With 5-5-5 Spacing, 1Mm Band Electrode , 8F Sensor Enabled Uni-Directional Circular Mapping Catheter With 3-3-3Mm & 5-5-5Mm Electrode Specification, 2Mm Tip & 1 Mm Band Electrode With Fixed Loop , 8F Sensor Enabled Bi-Directionalcircular Mapping Catheter Df Curve 3-3-3Mm- & 5-5-5Mm Specification, 2Mm Tip & 1 Mm Band Electrode With Fixed Loop , 8F Sensor Enabled Uni-Directional Circular Mapping Catheter With 6.5Mm Electrode Spacing Variable Loop With 15-25 Mm Range , 8F Sensor Enabled Bi-Directional Circular Mapping Catheter With 1-4-1 Mm Electrode Spacing Variable Loop With 15-25 Mm Range , 8F-Irrigated Bidirectional 16 Electrode ,2F Splines, 3 Mm Spacing , 1Mm Electrode Size,High Density Sensor Enable Mapping Cathter Comaptible With Ensite Mapping System , Bi-D-Deflectable Radio Frequency Ablation Catheter (7 F, 4Mm Tip ) 2-5-2 Electrode Spacing - With Universal Temperature Sensor (Thermocouple And Thermistor Temperature Monitoring Capability),Should Be Compatable To Use With Ibi T11 & Ampere Rf , Uni-D-Deflectable Radio Frequency Ablation Catheter (7 F, 4Mm Tip ) 2-5-2 Electrode Spacing, Usable Length 110Cm ,Should Be Compatable To Use With Ibi T11 & Ampere Rf , Uni-D-Deflectable Radio Frequency Ablation Catheter (5 F, 4Mm Tip ) 2-5-2 Electrode Spacing ,Should Be Compatable To Use With Ibi T11 & Ampere Rf , Irrigated Bi- Directional Ablation Catheter With Flexible Tip1-4-1, Symmetric And Asymmetric Option , Should Be Compatable To Use With Ibi T11 & Ampere Rf Generator , Irrigated Uni- Directional Ablation Catheter With Flexible Tip1-4-1, D And F Curve , Should Be Compatable To Use With Ibi T11 & Ampere Rf Generator , Contact Force Sensor Enable Catheter With Fiber Optic Technology For Force Detection 3.5 Mm Tip Electrode 8F , Six Saline Irrigation Hole, 2-2-2 Ring Spacing,Should Be Compatable To Use With Ibi T11 & Ampere Rf , Intracardiac Echo Catheter-9F Size ,Transducer Type 64 Element Phased Array , Viewing Sector 80 Degrees, Tip Deflection Anterior/Posterior, Left/Right +/- 120 Degree Flexion Compatible With Philips Cx50 Echo System , Magnetic & Impedance (Hybrid) Based Patches For Electroanotomical Mapping For Use With Ensite 3D Mapping System. , Magnetic Based Patches For Electroanotomical Mapping For Use With Ensite 3D Mapping System. , Cool Point Tubing Set For Irrigated Rf Catheter With Dedicated Pressure Sensor And Compatible With Abbott Coolpoint Pump , Cables For Fixed Quadripolar Electrophysiology Catheters , Cables For Fixed Decapolar Electrophysiology Catheters , Cables For Deflectable Decapolar Electrophysiology Catheters , Cables For Highdensity Mappingelectrophysiology Catheters Compatible With Ensite Mapping System , Cables For Ablation Range Ofelectrophysiology Catheters Compatible Compatable To Use With Ibi T11 & Ampere Rf , Cable For Fixed Loop Circular Mapping Catheters , Cable For Variable Loop Circular Mapping Catheters , Us Fda/Ce Approved Permanent Pacemakers With All Leads And Accessories ·Vvir ·All Single Chamber Modes And Basic Pacing Programmable Parameters ·Must Have Ventricular Capture Management ·The Size Of Lead Must Be 7F Or Less ·The Lead Must Be Steroid Eluting And Should Be Both Bipolar And Unipolar Configuration ·Must Have Both Active And Passive Fixation Endocardial Leads Available ··Direct Presence Of Parent Companyin India (Not Only Through The Distributors ) And Company Must Provide Its Trained Technical Person For Each Implantation When Ever Required And Forfollow Up Programming When It Is Required ·Company Must Provide At Least One Programmer Exclusively To The Cardiology Dept. ·Company Must Quote Only The Latest Model Of Devices Commercially Available , Dcgiapproved Permanent Pacemakers With All Leads And Accessories ·Vvir ·All Single Chamber Modes And Basic Pacing Programmable Parameters ·Must Have Ventricular Capture Management ·The Size Of Lead Must Be 7F Or Less ·The Lead Must Be Steroid Eluting And Should Be Both Bipolar And Unipolar Configuration ·Must Have Both Active And Passive Fixation Endocardial Leads Available ·Life Time Replacement Warranty. ·Direct Presence Of Parent Companyin India (Not Only Through The Distributors ) And Company Must Provide Its Trained Technical Person For Each Implantation When Ever Required And Forfollow Up Programming When It Is Required ·Company Must Provide At Least One Programmer Exclusively To The Cardiology Dept. ·Company Must Quote Only The Latest Model Of Devices Commercially Available , D.D.D Pacemaker With All Accessories- Dcgi & Fda Approved /Ce Approved , Dddr Mri Pacemaker With All Accessories -Dcgi & Us Fda/Ce Approved , Dddr Mri Pacemaker With All Accessories And Life Time Warranty -Dcgi & Us Fda/Ce Approved ·Latest And New 3T Full Body Mri, Beat To Beat Capture Mgt, ·Algorithm To Manage Neuro-Cardiogenic Syncope, ·Af Suppression, Optimization Of Av Delay, Congestion Monitoring. , Dicd-40J Deliver Fable Energy - -Dcgi & Us Fda Approved /Ce Approved , Crtp-Quadripolar-Egm Based Dynamic Av Delay Optimization-Dcgi & Us Fda Approved /Ce Approved ·Congestion Monitoring Algorithm ·Capture Management For All Chambers ·Option Of Triggered Biv Pacing During Af ·Capable Of Wireless Telemetry , Crtp-Multipoint Egm Based Dynamic Av Delay Optimization -Dcgi & Us Fda Approved /Ce Approved ·Lv Lead Able To Pace At Two Points In Lv In One Cycle ·Qudripolar Leadwith Mri Compitable Device ·Congestion Monitoring Algorithm ·Capture Management For All Chambers ·Option Of Triggered Biv Pacing During Af ·Capable Of Wireless Telemetry , Crt-D Quadriopolar Df-4 Fda/Ce Approved Latest And New 40J Deliver Fable Energy – -Dcgi & Us Fda Approved /Ce Approved ·Full Body Mri, Congestion Monitoringng Rv Lead 7F Or Less ·Af Suppression ·Egm Based Av Delay Optimization ·Mechanism For Narrow Qrs By Synchronizing Intrinsic And Paced Pulses , Crt-D Multipoint Df-4 Fda/Ce Approved Latest And New 40J Deliver Fable Energy- -Dcgi & Us Fda /Ce Approved ·Full Body Mri, Congestion Monitoringng Rv Lead 7F Or Less ·Af Suppression ·Egm Based Av Delay Optimization ·Mechanism For Narrow Qrs By Synchronizing Intrinsic And Paced Pulses , Us Fda/Ce Approved Permanent Pacemakers With All Leads And Accessories ·Ddd ·Allmodes And Basic Pacing Programmable Parameters Including Hystersis ·The Size Of Lead Must Be 6F Or Less ·The Lead Must Be Steroid Eluting And Should Be Both Bipolar And Unipolar Configuration ·Must Have Both Active And Passive Fixation Endocardial Leads Available ··Direct Presence Of Parent Companyin India (Not Only Through The Distributors ) And Company Must Provide Its Trained Technical Person For Each Implantation When Ever Required And Forfollow Up Programming When It Is Required ·Company Must Provide At Least One Programmer Exclusively To The Cardiology Dept. ·Company Must Quote Only The Latest Model Of Devices Commercially Available , Us Fda/Ce Approved Permanent Pacemakers With All Leads And Accessories ·Ddd ·Allmodes And Basic Pacing Programmable Parameters Including Hystersis ·The Size Of Lead Must Be 6F Or Less And With His Bundal Pacing Lead ·The Lead Must Be Steroid Eluting And Should Be Both Bipolar And Unipolar Configuration ·Must Have Both Active And Passive Fixation Endocardial Leads Available ·Direct Presence Of Parent Companyin India (Not Only Through The Distributors ) And Company Must Provide Its Trained Technical Person For Each Implantation When Ever Required And Forfollow Up Programming When It Is Required ·Company Must Provide At Least One Programmer Exclusively To The Cardiology Dept. ·Company Must Quote Only The Latest Model Of Devices Commercially Available , Dcgiapproved Permanent Pacemakers With All Leads And Accessories ·Ddd ·Allmodes And Basic Pacing Programmable Parameters Including Hystersis ·The Size Of Lead Must Be 6F Or Less And With His Bundal Pacing Lead ·The Lead Must Be Steroid Eluting And Should Be Both Bipolar And Unipolar Configuration ·Must Have Both Active And Passive Fixation Endocardial Leads Available · ·Direct Presence Of Parent Companyin India (Not Only Through The Distributors ) And Company Must Provide Its Trained Technical Person For Each Implantation When Ever Required And Forfollow Up Programming When It Is Required ·Company Must Provide At Least One Programmer Exclusively To The Cardiology Dept. ·Company Must Quote Only The Latest Model Of Devices Commercially Available , Dcgi Approved Permanent Pacemakers With All Leads And Accessories ·Ddd ·Allmodes And Basic Pacing Programmable Parameters Including Hystersis ·The Size Of Lead Must Be 6F Or Less - His/Lbba Pacing ·The Lead Must Be Steroid Eluting And Should Be Both Bipolar And Unipolar Configuration ·Must Have Both Active And Passive Fixation Endocardial Leads Available ·Life Time Replacement Warranty. ·Direct Presence Of Parent Companyin India (Not Only Through The Distributors ) And Company Must Provide Its Trained Technical Person For Each Implantation When Ever Required And Forfollow Up Programming When It Is Required ·Company Must Provide At Least One Programmer Exclusively To The Cardiology Dept. ·Company Must Quote Only The Latest Model Of Devices Commercially Available , Us Fda/Ce Approved Permanent Pacemakers With All Leads And Accessories ·Dddr ·Allsingle Modes And Basic Pacing Programmable Parameters And With Special Features ·Must Have Approved Algorithm For Atrial Fibrillation Suppression With Programmable Automatic Mode Switch Basel Rate. ·Must Have Ventricular Capture Management - Must Have Mri Compitable ·Must Have P & R Wave Measurement ·The Size Of Lead Must Be 6F Or Less ·The Lead Must Be Steroid Eluting And Should Be Both Bipolar And Unipolar Configuration ·Must Have Both Active And Passive Fixation Endocardial Leads Available ··Direct Presence Of Parent Companyin India (Not Only Through The Distributors ) And Company Must Provide Its Trained Technical Person For Each Implantation When Ever Required And Forfollow Up Programming When It Is Required ·Company Must Provide At Least One Programmer Exclusively To The Cardiology Dept. ·Company Must Quote Only The Latest Model Of Devices Commercially Available , Us Fda/Ce Approved Permanent Pacemakers With All Leads And Accessories ·Dddr ·Allmodes And Basic Pacing Programmable Parameters And Special Features ·Must Have Approved Af Suppression Algorithm & Fluid Monitoring. ·Must Have Ventricular Capture Management ·Must Have P & R Wave Measurement ·The Size Of Lead Must Be 6F Or Less ·The Lead Must Be Steroid Eluting And Should Be Both Bipolar And Unipolar Configuration ·Must Have Both Active And Passive Fixation Endocardial Leads Available ·Life Time Replacement Warranty. ·Direct Presence Of Parent Companyin India (Not Only Through The Distributors ) And Company Must Provide Its Trained Technical Person For Each Implantation When Ever Required And Forfollow Up Programming When It Is Required ·Company Must Provide At Least One Programmer Exclusively To The Cardiology Dept. ·Company Must Quote Only The Latest Model Of Devices Commercially Available , Us Fda/Ce Approved Permanent Pacemakers With All Leads And Accessories ·Dddr ·Allmodes And Basic Pacing Programmable Parameters And Special Features ··Must Have Ventricular Capture Management ·Must Have P & R Wave Measurement - Lbba Pacing System - Style Driven Lead ·The Size Of Lead Must Be 6F Or Less - Must Have Congestion Monitoring ·The Lead Must Be Steroid Eluting And Should Be Both Bipolar And Unipolar Configuration ·Have Feature For Optimization Of Av Delay ·Must Have Both Active And Passive Fixation Endocardial Leads Available ·Life Term Replacement Warranty. ·Direct Presence Of Parent Companyin India (Not Only Through The Distributors ) And Company Must Provide Its Trained Technical Person For Each Implantation When Ever Required And Forfollow Up Programming When It Is Required ·Company Must Provide At Least One Programmer Exclusively To The Cardiology Dept. ·Company Must Quote Only The Latest Model Of Devices Commercially Available , Aicd Single Chamber Pacemaker With All Leads - Us Fda/Ce Approved ,Icd With All Leads ·Single Chamber ·Rv Lead Must Be 7F Or Less - Must Have Mri Compitble ·All Basic Programmable Parameters ·Lead Should Be Steroid Eluting ·Should Have Both Active And Passive Fixation Leads ·Should Be Minimum 8+2 Year Warranty ·Direct Presence Of Parent Companyin India (Not Only Through The Distributors ) And Company Must Provide Its Trained Technical Person For Each Implantation When Ever Required And Forfollow Up Programming When It Is Required ·Company Must Provide At Least One Programmer Exclusively To The Cardiology Dept. ·Company Must Quote Only The Latest Model Of Devices Commercially Available , Aicd Single Chamber Pacemaker With All Leads – Dcgiapproved ,Icd With All Leads ·Single Chamber ·Rv Lead Must Be 7F Or Less - Must Have Mri Compitble ·All Basic Programmable Parameters ·Lead Should Be Steroid Eluting ·Should Have Both Active And Passive Fixation Leads ·Should Be Minimum 8+2 Year Warranty ·Direct Presence Of Parent Companyin India (Not Only Through The Distributors ) And Company Must Provide Its Trained Technical Person For Each Implantation When Ever Required And Forfollow Up Programming When It Is Required ·Company Must Provide At Least One Programmer Exclusively To The Cardiology Dept. ·Company Must Quote Only The Latest Model Of Devices Commercially Available. , Aicd Dual Chamber Pacemaker With All Leads -Us Fda/Ce Approved ,Icd With All Leads And All Accessories ·Dual Chamber ·Rv Lead Must Be 7F Or Less ·All Basic Programmable Parameters ·Lead Should Be Steroid Eluting ·Should Have Both Active And Passive Fixation Leads ·Should Be Minimum 5+3 Year Warranty ·Direct Presence Of Parent Companyin India (Not Only Through The Distributors ) And Company Must Provide Its Trained Technical Person For Each Implantation When Ever Required And Forfollow Up Programming When It Is Required ·Company Must Provide At Least One Programmer Exclusively To The Cardiology Dept. ·Company Must Quote Only The Latest Model Of Devices Commercially Available , Aicd Dual Chamber Pacemaker With All Leads- Dcgiapproved ,Icd With All Leads And All Accessories ·Dual Chamber ·Rv Lead Must Be 9F Or Less ·All Basic Programmable Parameters ·Lead Should Be Steroid Eluting ·Should Have Both Active And Passive Fixation Leads ·Should Be Minimum 5+3 Year Warranty ·Direct Presence Of Parent Companyin India (Not Only Through The Distributors ) And Company Must Provide Its Trained Technical Person For Each Implantation When Ever Required And Forfollow Up Programming When It Is Required ·Company Must Provide At Least One Programmer Exclusively To The Cardiology Dept. ·Company Must Quote Only The Latest Model Of Devices Commercially Available , Aicd Single Chamber Device With All Leads -Icd With All Leads And All Accessories - Dcgiand Us Fda/ Ce Approved ·Should Have Latest Bluetooth Technology Low Energy Communication Enabling Smart Phone Connectivity Through Secured Data Encryption. ·Should Have Multi Point Pacing Delivers Multiple Lv Pacing Pulse/Cardiac Cycle In Both Lv And Biv Pacing Modes. ·Should Have Improvised Sync-Av Pulse Crt Technology Offer Dynamic Av Timing. ·40 J Delivered Energy For Enhanced Safety Margin ·Should Have Full Body 3-Tesla Mri Compatibility. ·Direct Presence Of Parent Companyin India (Not Only Through The Distributors) And Company Must Provide Its Trained Technical Person For Each Implantation Whenever Required And Forfollow Up Programming When It Is Required. ·Company Must Provide At Least One Programmer Exclusively To The Cardiology Dept., ·Company Must Quote Only The Latest Model Of Devices Commercially Available. , Aicd Dual Chamber Device With All Leads -Icd With All Leads And All Accessories - Dcgiand Us Fda/ Ce Approved ·Should Have Latest Bluetooth Technology Low Energy Communication Enabling Smart Phone Connectivity Through Secured Data Encryption. ·Should Have Multi Point Pacing Delivers Multiple Lv Pacing Pulse/Cardiac Cycle In Both Lv And Biv Pacing Modes. ·Should Have Improvised Sync-Av Pulse Crt Technology Offer Dynamic Av Timing. ·40 J Delivered Energy For Enhanced Safety Margin ·Should Have Full Body 3-Tesla Mri Compatibility. ·Direct Presence Of Parent Companyin India (Not Only Through The Distributors) And Company Must Provide Its Trained Technical Person For Each Implantation Whenever Required And Forfollow Up Programming When It Is Required. ·Company Must Provide At Least One Programmer Exclusively To The Cardiology Dept., ·Company Must Quote Only The Latest Model Of Devices Commercially Available , Us Fda/Ce Approved, Biventricular Pacemaker With Atrial,Rv, Lv Leads And All Accessories Required During Implantation ·Must Have Separate Programmable Rv, Lv Lead Amplitude, Pulse Width And Vv Delay And Should Have Following Special Features ·Must Have Facility For Egm Based Optimization Of Av, Pv And Vv Delays ·The Size Of Atrial And Rv Leads Should Be 7F Or Less ·The Leads Should Be Steroid Eluting And Should Be Bipolar And Unkipolar Configuration ·Should Have Both Active And Passive Fixation Ra & Rv Endocardial Leads ·Should Have Epicardial Lead For Epicardial Lv Lead Implantation ·Replacement Warranty Not Less Than 5 Years ·Direct Presence Of Parent Companyin India (Not Only Through The Distributors ) And Company Must Provide Its Trained Technical Person For Each Implantation When Ever Required And Forfollow Up Programming When It Is Required ·Company Must Provide At Least One Programmer Exclusively To The Cardiology Dept. ·Company Must Quote Only The Latest Model Of Devices Commercially Available , Dcgiapproved, Biventricular Pacemaker With Atrial,Rv, Lv Leads And All Accessories Required During Implantation ·Must Have Separate Programmable Rv, Lv Lead Amplitude, Pulse Width And Vv Delay And Should Have Following Special Features ·Must Have Facility For Egm Based Optimization Of Av, Pv And Vv Delays ·The Size Of Atrial And Rv Leads Should Be 7F Or Less ·The Leads Should Be Steroid Eluting And Should Be Bipolar And Unkipolar Configuration ·Should Have Both Active And Passive Fixation Ra & Rv Endocardial Leads ·Should Have Epicardial Lead For Epicardial Lv Lead Implantation ·Replacement Warranty Not Less Than 5 Years ·Direct Presence Of Parent Companyin India (Not Only Through The Distributors ) And Company Must Provide Its Trained Technical Person For Each Implantation When Ever Required And Forfollow Up Programming When It Is Required ·Company Must Provide At Least One Programmer Exclusively To The Cardiology Dept. , Us Fda/Ce Approved Biventricular Pacemaker + Icd (Combo Device) With Atrial, Rv, Lv Leads And All Accessories Rquired During Impantation ·Must Have All Basic Programmable Parameters ·Must Have Separate Programmable Rv, Lv Lead Amplitude, Pulse Width And Vv Delay ·The Leads Should Be Steroid Eluting ·Should Have Both Active And Passive Fixation Ra & Rv Endocardial Leadsr - Rv Lead 7F Or Less ·Should Have Epicardial Lead For Epicardial Lv Lead Implantation ·Replacement Warranty Not Less Than 3 + 2 Years ·Direct Presence Of Parent Companyin India (Not Only Through The Distributors ) And Company Must Provide Its Trained Technical Person For Each Implantation When Ever Required And Forfollow Up Programming When It Is Required ·Company Must Provide At Least One Programmer Exclusively To The Cardiology Dept. ·Company Must Quote Only The Latest Model Of Devices Commercially Available , Dcgiapproved Biventricular Pacemaker + Icd (Combo Device) With Atrial, Rv, Lv Leads And All Accessories Rquired During Impantation ·Must Have All Basic Programmable Parameters ·Must Have Separate Programmable Rv, Lv Lead Amplitude, Pulse Width And Vv Delay ·The Leads Should Be Steroid Eluting ·Should Have Both Active And Passive Fixation Ra & Rv Endocardial Leads ·Should Have Epicardial Lead For Epicardial Lv Lead Implantation ·Replacement Warranty Not Less Than 3 + 2 Years ·Direct Presence Of Parent Companyin India (Not Only Through The Distributors ) And Company Must Provide Its Trained Technical Person For Each Implantation When Ever Required And Forfollow Up Programming When It Is Required ·Company Must Provide At Least One Programmer Exclusively To The Cardiology Dept. ·Company Must Quote Only The Latest Model Of Devices Commercially Available , Us Fda/Ce Approved Biventricular Pacemaker + Icd (Combo Device) With Atrial, Rv, Lv Leads And All Accessories Rquired During Impantation ·Must Have Quadripolar Lead For Lv Pacing ·Must Have All Basic Programmable Parameters With Following Special Features ·Facility Of Atp During Charging For Defibrillation ·Must Have Separate Programmable Rv, Lv Lead Amplitude, Pulse Width And Vv Delay ·Must Have Fluidmonitoring System - Rv Lead 7F Or Less ·The Leads Should Be Steroid Eluting ·Should Have Both Active And Passive Fixation Ra & Rv Endocardial Leads ·Should Have Epicardial Lead For Epicardial Lv Lead Implantation ·Replacement Warranty Not Less Than 3 + 2 Years ·Direct Presence Of Parent Companyin India (Not Only Through The Distributors ) And Company Must Provide Its Trained Technical Person For Each Implantation When Ever Required And Forfollow Up Programming When It Is Required ·Company Must Provide At Least One Programmer Exclusively To The Cardiology Dept. , Dcgiapproved Biventricular Pacemaker + Icd (Combo Device) With Atrial, Rv, Lv Leads And All Accessories Rquired During Impantation ·Must Have Quadripolar Lead For Lv Pacing ·Must Have All Basic Programmable Parameters With Following Special Features ·Facility Of Atp During Charging For Defibrillation ·Must Have Separate Programmable Rv, Lv Lead Amplitude, Pulse Width And Vv Delay ·Must Have Fluidmonitoring System ·The Leads Should Be Steroid Eluting ·Should Have Both Active And Passive Fixation Ra & Rv Endocardial Leads ·Should Have Epicardial Lead For Epicardial Lv Lead Implantation ·Replacement Warranty Not Less Than 3 + 2 Years ·Direct Presence Of Parent Companyin India (Not Only Through The Distributors ) And Company Must Provide Its Trained Technical Person For Each Implantation When Ever Required And Forfollow Up Programming When It Is Required ·Company Must Provide At Least One Programmer Exclusively To The Cardiology Dept. ·Company Must Quote Only The Latest Model Of Devices Commercially Available , Us Fda/Ce Approved Biventricular Pacemaker + Icd (Combo Device) With Atrial, Rv, Lv Leads And All Accessories Rquired During Impantation ·Must Have Separate Programmable Rv, Lv Lead Amplitude, Pulse Width And Vv Delay And Shouldhave Following Special Feature ·The Lv Lead Must Be Quadripolar. - Rv Lead Must Be 7F Or Less ·The Leads Should Be Steroid Elutingand Should Be Both Bipolar And Unipolar ·Should Have Both Active And Passive Fixation Ra & Rv Endocardial Leads ·Should Have Epicardial Lead For Epicardial Lv Lead Implantation ·Replacement Warranty Not Less Than 3 + 2 Years ·Direct Presence Of Parent Companyin India (Not Only Through The Distributors ) And Company Must Provide Its Trained Technical Person For Each Implantation When Ever Required And Forfollow Up Programming When It Is Required ·Company Must Provide At Least One Programmer Exclusively To The Cardiology Dept. ·Company Must Quote Only The Latest Model Of Devices Commercially Available , Dcgiapproved Biventricular Pacemaker + Icd (Combo Device) With Atrial, Rv, Lv Leads And All Accessories Rquired During Impantation ·Must Have Separate Programmable Rv, Lv Lead Amplitude, Pulse Width And Vv Delay And Shouldhave Following Special Feature ·The Lv Lead Must Be Quadripolar. ·The Leads Should Be Steroid Elutingand Should Be Both Bipolar And Unipolar ·Should Have Both Active And Passive Fixation Ra & Rv Endocardial Leads ·Should Have Epicardial Lead For Epicardial Lv Lead Implantation ·Replacement Warranty Not Less Than 3 + 2 Years ·Direct Presence Of Parent Companyin India (Not Only Through The Distributors ) And Company Must Provide Its Trained Technical Person For Each Implantation When Ever Required And Forfollow Up Programming When It Is Required ·Company Must Provide At Least One Programmer Exclusively To The Cardiology Dept. ·Company Must Quote Only The Latest Model Of Devices Commercially Available , Lead Less Pacemaker With All Accessories.–Dcgiand Us Fda/ Ce Approved Vvi, Mri Compitable Must Have Retrievable Option , Lead Less Pacemaker With All Accessories.–Dcgiand Us Fda/ Ce Approved Ddd Mri Compitable Must Have Retrievable Option , Crt- D Combo Device With All Leads -Icd With All Leads And All Accessories - Dcgiand Us Fda/ Ce Approved ·Should Have Latest Bluetooth Technology Low Energy Communication Enabling Smart Phone Connectivity Through Secured Data Encryption. ·Should Have Multi Point Pacing Delivers Multiple Lv Pacing Pulse/Cardiac Cycle In Both Lv And Biv Pacing Modes. ·Should Have Improvised Sync-Av Pulse Crt Technology Offer Dynamic Av Timing. ·40 J Delivered Energy For Enhanced Safety Margin ·Should Have Full Body 3-Tesla Mri Compatibility. , Dcgiapproved Permanent Pacemakers With All Leads And Accessories Vvi ? All Single Chamber Modes And Basic Pacing Programmable Parameters ? The Size Of Lead Must Be 7F Or Less ? The Lead Must Be Steroid Eluting And Should Be Both Bipolar And Unipolar Configuration ? Must Have Both Active And Passive Fixation Endocardial Leads Available ? Life Time Replacement Warranty. ? Direct Presence Of Parent Companyin India (Not Only Through The Distributors ) And Company Must Provide Its Trained Technical Person For Each Implantation When Ever Required And Forfollow Up Programming When It Is Required ? Company Must Provide At Least One Programmer Exclusively To The Cardiology Dept. ? Company Must Quote Only The Latest Model Of Devices Commercially Available , Us Fda/Ce Approved Permanent Pacemakers With All Leads And Accessories ? Vvir ? All Single Chamber Modes And Basic Pacing Programmable Parameters ? Must Have Mri Compatible ? Must Have Programmable Sensor Control Rest Rate ? Must Have Ventricular Capture Management ? The Size Of Lead Must Be 8F Or Less ? The Lead Must Be Steroid Eluting And Should Be Both Bipolar And Uni-Polar Configuration ? Must Have Both Active And Passive Fixation Endo-Cardial Leads Available ? Life Time Replacement Warranty. ? Direct Presence Of Parent Companyin India (Not Only Through The Distributors ) And Company Must Provide Its Trained Technical Person For Each Implantation When Ever Required And Forfollow Up Programming When It Is Required , Dcgiapproved Permanent Pacemakers With All Leads And Accessories Vvir ? All Single Chamber Modes And Basic Pacing Programmable Parameters ? Must Have Mri Compatible ? Must Have Programmable Sensor Control Rest Rate ? Must Have Ventricular Capture Management ? The Size Of Lead Must Be 8F Or Less ? The Lead Must Be Steroid Eluting And Should Be Both Bipolar And Uni-Polar Configuration ? Must Have Both Active And Passive Fixation Endo- Cardial Leads Available ? Life Time Replacement Warranty. ? Direct Presence Of Parent Companyin India (Not Only Through The Distributors ) And Company Must Provide Its Trained Technical Person For Each Implantation When Ever Required And Forfollow Up Programming When It Is Required ? Company Must Provide At Least One Programmer Exclusively To The Cardiology Dept. ?Company Must Quote Only The Latest Model Of Devices Commercially Available , Us Fda/Ce Approved Permanent Pacemakers With All Leads And Accessories • Vvir • All Single Chamber Modes And Basic Pacing Programmable Parameters • Must Have Mri Compatible • Must Have Programmable Sensor Control Rest Rate • Must Have Ventricular Capture Management • The Size Of Lead Must Be 8F Or Less • The Lead Must Be Steroid Eluting And Should Be Both Bipolar And Uni-Polar Configuration • Must Have Both Active And Passive Fixation Endo-Cardial Leads Available • Life Time Replacement Warranty. • Direct Presence Of Parent Company In India (Not Only Through The Distributors ) And Company Must Provide Its Trained Technical Person For Each Implantation When Ever Required And For Follow Up Programming When It Is Required • Company Must Provide At Least One Programmer Exclusively To The Cardiology Dept. Company Must Quote Only The Latest Model Of Devices Commercially Available. , V.V.I Pacemaker With All Accessories And Life Time Warranty -Dcgi & Us Fda/Ce Approved • Latest And New Full Body Mri, Beat To Beat Capture Mgt, , D.D.D Pacemaker With All Accessories And Life Time Warranty- Dcgi & Fda Approved /Ce Approved , Dddr Mri Pacemaker With All Accessories And Life Time Warranty -Dcgi & Us Fda/Ce Approved , Sicd (Aicd) Df1 Connector--Dcgi & Us Fda Approved /Ce , Dicd-40J Deliver Fable Energy - -Dcgi & Us Fda Approved /Ce Approved , Crtp-Quadripolar-Egm Based Dynamic Av Delay Optimization-Dcgi & Us Fda Approved /Ce Approved ? Congestion Monitoring Algorithm ? Capture Management For All Chambers ? Option Of Triggered Biv Pacing During Af, ? Capable Of Wireless Telemetry , Crt-D Quadriopolar Df-4 Fda/Ce Approved Latest And New 40J Deliver Fable Energy – -Dcgi & Us Fda Approved /Ce Approved ·Full Body Mri, Congestion Monitoringng ·Af Suppression ·Egm Based Av Delay Optimization ·Mechanism For Narrow Qrs By Synchronizing Intrinsic And Paced Pulses , Crt-D Multipoint Df-4 Fda/Ce Approved Latest And New 40J Deliver Fable Energy- -Dcgi & Us Fda /Ce Approved ·Full Body Mri, Congestion Monitoringng ·Af Suppression ·Egm Based Av Delay Optimization ·Mechanism For Narrow Qrs By Synchronizing Intrinsic And Paced Pulses , Sub-Cutenous Icd Implant (Sc- I.C.D.)With All Accessories- Dcgi & Us Fda Approved /Ce Approved , Permanent Pacemakers With All Leads And Accessories - Us Fda/Ce Approved ? Vdd ? All Vdd & Single Chamber Modes And Basic Pacing Programmable Parameters And With Following Special Features ? Must Have Ventricular Capture Management ? The Size Of Lead Must Be 9F Or Less ? The Lead Must Be Steroid Eluting And Should Be Both Bipolar Configuration ? Having Passive Fixation Endocardial Leads Available ? Life Time Replacement Warranty. ? Direct Presence Of Parent Companyin India (Not Only Through The Distributors ) And Company Must Provide Its Trained ? Technical Person For Each Implantation When Ever Required And Forfollow Up Programming When It Is Required ? Company Must Provide At Least One Programmer Exclusively To The Cardiology Dept. Company Must Quote Only The Latest Model Of Devices Commercially Available. , Permanent Pacemakers With All Leads And Accessories - Dcgiapproved ? Vdd ? All Vdd & Single Chamber Modes And Basic Pacing Programmable Parameters And With Following Special Features ? Must Have Ventricular Capture Management ? The Size Of Lead Must Be 9F Or Less ? The Lead Must Be Steroid Eluting And Should Be Both Bipolar Configuration ? Having Passive Fixation Endocardial Leads Available ? Life Time Replacement Warranty. ? Direct Presence Of Parent Companyin India (Not Only Through The Distributors ) And Company Must Provide Its Trained ? Technical Person For Each Implantation When Ever Required And Forfollow Up Programming When It Is Required ? Company Must Provide At Least One Programmer Exclusively To The Cardiology Dept. ?Company Must Quote Only The Latest Model Of Devices Commercially Available , Us Fda/Ce Approved Permanent Pacemakers With All Leads And Accessories ? Ddd ? Allmodes And Basic Pacing Programmable Parameters Including Hystersis ? The Size Of Lead Must Be 7F Or Less ? The Lead Must Be Steroid Eluting And Should Be Both Bipolar And Unipolar Configuration ? Must Have Both Active And Passive Fixation Endocardial Leads Available ? Life Time Replacement Warranty. ? Direct Presence Of Parent Companyin India (Not Only Through The Distributors ) And Company Must Provide Its Trained Technical Person For Each Implantation When Ever Required And Forfollow Up Programming When It Is Required ? Company Must Provide At Least One Programmer Exclusively To The Cardiology Dept. ? Company Must Quote Only The Latest Model Of Devices Commercially Available , Dcgiapproved Permanent Pacemakers With All Leads And Accessories ? Ddd ? Allmodes And Basic Pacing Programmable Parameters Including Hystersis ? The Size Of Lead Must Be 7F Or Less ? The Lead Must Be Steroid Eluting And Should Be Both Bipolar And Unipolar Configuration ? Must Have Both Active And Passive Fixation Endocardial Leads Available ? Life Time Replacement Warranty. ? Direct Presence Of Parent Companyin India (Not Only Through The Distributors ) And Company Must Provide Its Trained Technical Person For Each Implantation When Ever Required And Forfollow Up Programming When It Is Required ? Company Must Provide At Least One Programmer Exclusively To The Cardiology Dept. ? Company Must Quote Only The Latest Model Of Devices Commercially Available , Us Fda/Ce Approved Permanent Pacemakers With All Leads And Accessories ? Dddr ? Allsingle Modes And Basic Pacing Programmable Parameters And With Special Features ? Must Have Approved Algorithm For Atrial Fibrillation Suppression With Programmable Automatic Mode Switch Basel Rate. ? Must Have Ventricular Capture Management ? Must Have P & R Wave Measurement ? The Size Of Lead Must Be 7F Or Less ? The Lead Must Be Steroid Eluting And Should Be Both Bipolar And Unipolar Configuration ? Must Have Both Active And Passive Fixation Endocardial Leads Available ? Life Time Replacement Warranty. ? Direct Presence Of Parent Companyin India (Not Only Through The Distributors ) And Company Must Provide Its Trained Technical Person For Each Implantation When Ever Required And Forfollow Up Programming When It Is Required ? Company Must Provide At Least One Programmer Exclusively To The Cardiology Dept. ? Company Must Quote Only The Latest Model Of Devices Commercially Available , Us Fda/Ce Approved Permanent Pacemakers With All Leads And Accessories ? Dddr ? Allmodes And Basic Pacing Programmable Parameters And Special Features ? Must Have Approved Atrial Tachycardia Management Algorithm & Fluid Monitoring. ? Must Have Ventricular Capture Management ? Must Have P & R Wave Measurement ? The Size Of Lead Must Be 7F Or Less ? The Lead Must Be Steroid Eluting And Should Be Both Bipolar And Unipolar Configuration ? Must Have Both Active And Passive Fixation Endocardial Leads Available ? Life Time Replacement Warranty. ? Direct Presence Of Parent Companyin India (Not Only Through The Distributors ) And Company Must Provide Its Trained Technical Person For Each Implantation When Ever Required And Forfollow Up Programming When It Is Required ? Company Must Provide At Least One Programmer Exclusively To The Cardiology Dept. ? Company Must Quote Only The Latest Model Of Devices Commercially Available , Aicd Single Chamber Pacemaker With All Leads - Us Fda/Ce Approved ,Icd With All Leads Single Chamber ? Rv Lead Must Be 9F Or Less ? All Basic Programmable Parameters ? Lead Should Be Steroid Eluting ? Should Have Both Active And Passive Fixation Leads ? Should Be Minimum 5+3 Year Warranty ? Direct Presence Of Parent Companyin India (Not Only Through The Distributors ) And Company Must Provide Its Trained Technical Person For Each Implantation When Ever Required And Forfollow Up Programming When It Is Required ? Company Must Provide At Least One Programmer Exclusively To The Cardiology Dept. ? Company Must Quote Only The Latest Model Of Devices Commercially Available , Aicd Single Chamber Pacemaker With All Leads – Dcgiapproved ,Icd With All Leads ? Single Chamber ? Rv Lead Must Be 9F Or Less ? All Basic Programmable Parameters ? Lead Should Be Steroid Eluting ? Should Have Both Active And Passive Fixation Leads ? Should Be Minimum 5+3 Year Warranty ? Direct Presence Of Parent Companyin India (Not Only Through The Distributors ) And Company Must Provide Its Trained Technical Person For Each Implantation When Ever Required And Forfollow Up Programming When It Is Required ? Company Must Provide At Least One Programmer Exclusively To The Cardiology Dept. ? Company Must Quote Only The Latest Model Of Devices Commercially Available. , Aicd Dual Chamber Pacemaker With All Leads -Us Fda/Ce Approved ,Icd With All Leads And All Accessories ? Dual Chamber ? Rv Lead Must Be 9F Or Less ? All Basic Programmable Parameters ? Lead Should Be Steroid Eluting ? Should Have Both Active And Passive Fixation Leads ? Should Be Minimum 5+3 Year Warranty ? Direct Presence Of Parent Companyin India (Not Only Through The Distributors ) And Company Must Provide Its Trained Technical Person For Each Implantation When Ever Required And Forfollow Up Programming When It Is Required ? Company Must Provide At Least One Programmer Exclusively To The Cardiology Dept. ? Company Must Quote Only The Latest Model Of Devices Commercially Available , Aicd Dual Chamber Pacemaker With All Leads- Dcgiapproved ,Icd With All Leads And All Accessories ? Dual Chamber ? Rv Lead Must Be 9F Or Less ? All Basic Programmable Parameters ? Lead Should Be Steroid Eluting ? Should Have Both Active And Passive Fixation Leads ? Should Be Minimum 5+3 Year Warranty ? Direct Presence Of Parent Companyin India (Not Only Through The Distributors ) And Company Must Provide Its Trained Technical Person For Each Implantation When Ever Required And Forfollow Up Programming When It Is Required ? Company Must Provide At Least One Programmer Exclusively To The Cardiology Dept. ? Company Must Quote Only The Latest Model Of Devices Commercially Available , Aicd Dual Chamber Pacemaker With All Leads- Us Fda/Ce Approved ,Icd With All Leads And All Accessories ? Dual Chamber ? All Basic Programmable Parameters ? Must Have Shockreduction Technology With Fluid Monitoring ? Lead Should Be Steroid Eluting ? Lead Should Be Df-1& Df-4 Compatible ? Replacement Warranty As Per Norms ? Direct Presence Of Parent Companyin India (Not Only Through The Distributors ) And Company Must Provide Its Trained Technical Person For Each Implantation When Ever Required And Forfollow Up Programming When It Is Required ? Company Must Provide At Least One Programmer Exclusively To The Cardiology Dept. , Aicd Dual Chamber Pacemaker With All Leads - Dcgi Approved, Icd With All Leads And All Accessories ? Dual Chamber ? All Basic Programmable Parameters ? Must Have Shockreduction Technology With Fluid Monitoring ? Lead Should Be Steroid Eluting ? Lead Should Be Df-1& Df-4 Compatible ? Replacement Warranty As Per Norms ? Direct Presence Of Parent Companyin India (Not Only Through The Distributors ) And Company Must Provide Its Trained Technical Person For Each Implantation When Ever Required And Forfollow Up Programming When It Is Required ? Company Must Provide At Least One Programmer Exclusively To The Cardiology Dept. ? Company Must Quote Only The Latest Model Of Devices Commercially Available , D/C Icd Single Chamber Device Mri With All Leads And All Accessories - Dcgiand Us Fda/ Ce Approved ? Should Have Advanced Feature Of Automatic Av Search, And Adjustable Av Delay Etc. ? Direct Presence Of Parent Company In India (Not Only Through The Distributors) And Company Must Provide Its Trained Technical Person For Each Implantation Whenever Required And For Follow Up Programming When It Is Required. ? Company Must Provide At Least One Programmer Exclusively To The Cardiology Dept., ? Company Must Quote Only The Latest Model Of Devices Commercially Available. , S/C Icd Single Chamber Device Mri With All Leads And All Accessories - Dcgiand Us Fda/ Ce Approved ? Should Have Labelled Projected Longevity Of > 12Years With Warranty Not Less Than 8 + 2 Years. ? Direct Presence Of Parent Company In India (Not Only Through The Distributors) And Company Must Provide Its Trained Technical Person For Each Implantation Whenever Required And For Follow Up Programming When It Is Required. ? Company Must Provide At Least One Programmer Exclusively To The Cardiology Dept., ? Company Must Quote Only The Latest Model Of Devices Commercially Available. , Us Fda/Ce Approved Implantable Loop Recorder ? Must Be Able To Detect Asystole, Brady Arrhythmia And Vt/Fvt ? Must Have The Storage Capacity Of >45 Minutes. ? Must Have Dynamic Sensing Threshold For R Wave Sensing Along With Noise Reversion ? Must Have A Patient Tool For Symptomatic Recording ? Must Have At Least 35 Months Of Longevity ? Must Be Compatible With Remote Monitoring Devices, ? Direct Presence Of Parent Companyin India (Not Only Through The Distributors ) And Company Must Provide Its Trained Technical Person For Each Implantation Whenever Required And Forfollow Up Programming When It Is Required ? Company Must Provide At Least One Programmer Exclusively To The Cardiology Dept. ? Company Must Quote Only The Latest Model Of Devices Commercially Available , Dcgi Approved Implantable Loop Recorder ? Must Be Able To Detect Asystole, Bradyarrhythmia And Vt/Fvt ? Must Have The Storage Capacity Of >45 Minutes. ? Must Have Dynamic Sensing Threshold For R Wave Sensing Along With Noise Reversion ? Must Have A Patient Tool For Symptomatic Recording ? Must Have At Least 35 Months Of Longevity ? Must Be Compatible With Remote Monitoring Devices ? Direct Presence Of Parent Companyin India (Not Only Through The Distributors ) And Company Must Provide Its Trained Technical Person For Each Implantation Whenever Required And Forfollow Up Programming When It Is Required ? Company Must Provide At Least One Programmer Exclusively To The Cardiology Dept. ? Company Must Quote Only The Latest Model Of Devices Commercially Available , Us Fda/Ce Approved Implantable Loop Recorder For Af Detection ? Must Be Able To Detect Asystole, Bradyarrhythmia, Vt/Fvt And At/Af ? Must Have The Storage Capacity Of >45 Minutes. ? Must Have Dynamic Sensing Threshold For R Wave Sensing Along With Noise Reversion ? Must Have A Patient Tool For Symptomatic Recording Along With Alerts. ? Must Be Able To Give Af Burden Reports To Monitor The Progress Of Chronic Af Patients. ? Must Have At Least 35 Months Of Longevity ? Must Be Compatible With Remote Monitoring Devices ? Direct Presence Of Parent Companyin India (Not Only Through The Distributors ) And Company Must Provide Its Trained Technical Person For Each Implantation Whenever Required And Forfollow Up Programming When It Is Required ? Company Must Provide At Least One Programmer Exclusively To The Cardiology Dept. ? Company Must Quote Only The Latest Model Of Devices Commercially Available , ? Dcgi Approved Implantable Loop Recorder For Af Detection ?Must Be Able To Detect Asystole, Brady-Arrhythmia, Vt/Fvt And At/Af ? Must Have The Storage Capacity Of >45 Minutes. ? Must Have Dynamic Sensing Threshold For R Wave Sensing Along With Noise Reversion ? Must Have A Patient Tool For Symptomatic Recording Along With Alerts. ? Must Be Able To Give Af Burden Reports To Monitor The Progress Of Chronic Af Patients. ? Must Have At Least 35 Months Of Longevity ? Must Be Compatible With Remote Monitoring Devices, ? Direct Presence Of Parent Companyin India (Not Only Through The Distributors ) And Company Must Provide Its Trained Technical Person For Each Implantation Whenever Required And Forfollow Up Programming When It Is Required ? Company Must Provide At Least One Programmer Exclusively To The Cardiology Dept. ? Company Must Quote Only The Latest Model Of Devices Commercially Available , Us Fda/Ce Approved, Biventricular Pacemaker With Atrial,Rv, Lv Leads And All Accessories Required During Implantation ? Must Have Separate Programmable Rv, Lv Lead Amplitude, Pulse Width And Vv Delay And Should Have Following Special Features ? Must Have Facility For Egm Based Optimization Of Av, Pv And Vv Delays ? The Size Of Atrial And Rv Leads Should Be 7F Or Less ? The Leads Should Be Steroid Eluting And Should Be Bipolar And Unkipolar Configuration ? Should Have Both Active And Passive Fixation Ra & Rv Endocardial Leads ? Should Have Epicardial Lead For Epicardial Lv Lead Implantation ? Replacement Warranty Not Less Than 5 Years ? Direct Presence Of Parent Companyin India (Not Only Through The Distributors ) And Company Must Provide Its Trained Technical Person For Each Implantation When Ever Required And Forfollow Up Programming When It Is Required ? Company Must Provide At Least One Programmer Exclusively To The Cardiology Dept. ? Company Must Quote Only The Latest Model Of Devices Commercially Available , Dcgiapproved, Biventricular Pacemaker With Atrial,Rv, Lv Leads And All Accessories Required During Implantation ? Must Have Separate Programmable Rv, Lv Lead Amplitude, Pulse Width And Vv Delay And Should Have Following Special Features ? Must Have Facility For Egm Based Optimization Of Av, Pv And Vv Delays ? The Size Of Atrial And Rv Leads Should Be 7F Or Less ? The Leads Should Be Steroid Eluting And Should Be Bipolar And Unkipolar Configuration ? Should Have Both Active And Passive Fixation Ra & Rv Endocardial Leads ? Should Have Epicardial Lead For Epicardial Lv Lead Implantation ? Replacement Warranty Not Less Than 5 Years ? Direct Presence Of Parent Companyin India (Not Only Through The Distributors ) And Company Must Provide Its Trained Technical Person For Each Implantation When Ever Required And Forfollow Up Programming When It Is Required ? Company Must Provide At Least One Programmer Exclusively To The Cardiology Dept. ? Company Must Quote Only The Latest Model Of Devices Commercially Available , Us Fda/Ce Approved Biventricular Pacemaker + Icd (Combo Device) With Atrial, Rv, Lv Leads And All ? Accessories Rquired During Impantation ? Must Have All Basic Programmable Parameters ? Must Have Separate Programmable Rv, Lv Lead Amplitude, Pulse Width And Vv Delay ? The Leads Should Be Steroid Eluting ? Should Have Both Active And Passive Fixation Ra & Rv Endocardial Leads ? Should Have Epicardial Lead For Epicardial Lv Lead Implantation ? Replacement Warranty Not Less Than 3 + 2 Years ? Direct Presence Of Parent Companyin India (Not Only Through The Distributors ) And Company Must Provide Its Trained Technical Person For Each Implantation When Ever Required And Forfollow Up Programming When It Is Required ? Company Must Provide At Least One Programmer Exclusively To The Cardiology Dept. ? Company Must Quote Only The Latest Model Of Devices Commercially Available , Dcgiapproved Biventricular Pacemaker + Icd (Combo Device) With Atrial, Rv, Lv Leads And All Accessories ? Rquired During Impantation ? Must Have All Basic Programmable Parameters ? Must Have Separate Programmable Rv, Lv Lead Amplitude, Pulse Width And Vv Delay ? The Leads Should Be Steroid Eluting ? Should Have Both Active And Passive Fixation Ra & Rv Endocardial Leads ? Should Have Epicardial Lead For Epicardial Lv Lead Implantation ? Replacement Warranty Not Less Than 3 + 2 Years ? Direct Presence Of Parent Companyin India (Not Only Through The Distributors ) And Company Must Provide Its Trained Technical Person For Each Implantation When Ever Required And Forfollow Up Programming When It Is Required ? Company Must Provide At Least One Programmer Exclusively To The Cardiology Dept. ? Company Must Quote Only The Latest Model Of Devices Commercially Available , Us Fda/Ce Approved, Biventricular Pacemaker + Icd (Combo Device) Without Lead • Must Have All Basic Programmable Parameters • Should Have All Parameters Shown In Related Group Of Pacemaker • Replacement Warranty Not Less Than 5 Years • Direct Presence Of Parent Companyin India (Not Only Through The Distributors ) And Company Must Provide Its Trained Technical Person For Each Implantation When Ever Required And Forfollow Up Programming When It Is Required • Company Must Provide At Least One Programmer Exclusively To The Cardiology Dept. • Company Must Quote Only The Latest Model Of Devices Commercially Available , Dcgi Approved, Biventricular Pacemaker + Icd (Combo Device) Without Lead ? Must Have All Basic Programmable Parameters •Should Have All Parameters Shown In Related Group Of Pacemaker •Replacement Warranty Not Less Than 5 Years •Direct Presence Of Parent Companyin India (Not Only Through The Distributors ) And Company Must Provide Its Trained Technical Person For Each Implantation When Ever Required And Forfollow Up Programming When It Is Required •Company Must Provide At Least One Programmer Exclusively To The Cardiology Dept. ? • Company Must Quote Only The Latest Model Of Devices Commercially Available , Us Fda/Ce Approved, Biventricular Pacemaker (Crt) Without Lead ? Must Have All Basic Programmable Parameters ? Should Have All Parameters Shown In Related Group Of Pacemaker ? Replacement Warranty Not Less Than 5 Years ? Direct Presence Of Parent Companyin India (Not Only Through The Distributors ) And Company Must Provide Its Trained Technical Person For Each Implantation When Ever Required And Forfollow Up Programming When It Is Required ? Company Must Provide At Least One Programmer Exclusively To The Cardiology Dept. ? Company Must Quote Only The Latest Model Of Devices Commercially Available , Dcgi Approved, Biventricular Pacemaker (Crt) Without Lead ? Must Have All Basic Programmable Parameters ? Should Have All Parameters Shown In Related Group Of Pacemaker ? Replacement Warranty Not Less Than 5 Years ? Direct Presence Of Parent Companyin India (Not Only Through The Distributors ) And Company Must Provide Its Trained Technical Person For Each Implantation When Ever Required And Forfollow Up Programming When It Is Required ? Company Must Provide At Least One Programmer Exclusively To The Cardiology Dept. ? Company Must Quote Only The Latest Model Of Devices Commercially Available , Us Fda/Ce Approved, Aicd Dual Chamber Pacemaker Without Lead ? Must Have All Basic Programmable Parameters ? Should Have All Parameters Shown In Related Group Of Pacemaker ? Replacement Warranty Not Less Than 5 Years ? Direct Presence Of Parent Companyin India (Not Only Through The Distributors ) And Company Must Provide Its Trained Technical Person For Each Implantation When Ever Required And Forfollow Up Programming When It Is Required ? Company Must Provide At Least One Programmer Exclusively To The Cardiology Dept. ? Company Must Quote Only The Latest Model Of Devices Commercially Available , Dcgiapproved, Aicd Dual Chamber Pacemaker Without Lead ? Must Have All Basic Programmable Parameters ? Should Have All Parameters Shown In Related Group Of Pacemaker ? Replacement Warranty Not Less Than 5 Years ? Direct Presence Of Parent Companyin India (Not Only Through The Distributors ) And Company Must Provide Its Trained Technical Person For Each Implantation When Ever Required And Forfollow Up Programming When It Is Required ? Company Must Provide At Least One Programmer Exclusively To The Cardiology Dept. ? Company Must Quote Only The Latest Model Of Devices Commercially Available , Us Fda/Ce Approved, Aicd Singlechamber Pacemaker Without Lead ?Must Have All Basic Programmable Parameters ? Should Have All Parameters Shown In Related Group Of Pacemaker ? Replacement Warranty Not Less Than 5 Years ? Direct Presence Of Parent Companyin India (Not Only Through The Distributors ) And Company Must Provide Its Trained Technical Person For Each Implantation When Ever Required And Forfollow Up Programming When It Is Required ? Company Must Provide At Least One Programmer Exclusively To The Cardiology Dept. ? Company Must Quote Only The Latest Model Of Devices Commercially Available , Dcgiapproved, Aicd Singlechamber Pacemaker Without Lead ? Must Have All Basic Programmable Parameters ? Should Have All Parameters Shown In Related Group Of Pacemaker ? Replacement Warranty Not Less Than 5 Years ? Direct Presence Of Parent Companyin India (Not Only Through The Distributors ) And Company Must Provide Its Trained Technical Person For Each Implantation When Ever Required And Forfollow Up Programming When It Is Required ? Company Must Provide At Least One Programmer Exclusively To The Cardiology Dept. ? Company Must Quote Only The Latest Model Of Devices Commercially Available , ? Us Fda/Ce Approved, Vdd/Vddr Permanent Pacemaker Without Lea ? Vdd/Vddr ? All Vdd & Single Chamber Modes And Basic Pacingprogrammable Parameters And With Following Special Features ? Should Have All Parameters Shown In Related Group Of Pacemaker ? Life Term Replacement Warranty ? Direct Presence Of Parent Companyin India (Not Only Through The Distributors ) And Company Must Provide Its Trained Technical Person For Each Implantation When Ever Required And Forfollow Up Programming When It Is Required ? Company Must Provide At Least One Programmer Exclusively To The Cardiology Dept. ? Company Must Quote Only The Latest Model Of Devices Commercially Available , Dcgiapproved, Vdd/Vddr Permanent Pacemaker Without Lead ? Vdd/Vddr ? All Vdd & Single Chamber Modes And Basic Pacingprogrammable Parameters And With Following Special Features ? Should Have All Parameters Shown In Related Group Of Pacemaker ? Life Term Replacement Warranty ? Direct Presence Of Parent Companyin India (Not Only Through The Distributors ) And Company Must Provide Its Trained Technical Person For Each Implantation When Ever Required And Forfollow Up Programming When It Is Required ? Company Must Provide At Least One Programmer Exclusively To The Cardiology Dept. ? Company Must Quote Only The Latest Model Of Devices Commercially Available , Us Fda/Ce Approved, Ddd Permanent Pacemaker Without Lead ? Ddd ? All Modes And Basic Pacingprogrammable Parameters Including Hysteresis ? Should Have All Parameters Shown In Related Group Of Pacemaker ? Life Term Replacement Warranty ? Direct Presence Of Parent Companyin India (Not Only Through The Distributors ) And Company Must Provide Its Trained Technical Person For Each Implantation When Ever Required And Forfollow Up Programming When It Is Required ? Company Must Provide At Least One Programmer Exclusively To The Cardiology Dept. ? Company Must Quote Only The Latest Model Of Devices Commercially Available , Dcgiapproved, Ddd Permanent Pacemaker Without Lead ? Ddd ? All Modes And Basic Pacingprogrammable Parameters Including Hysteresis ? Should Have All Parameters Shown In Related Group Of Pacemaker ? Life Term Replacement Warranty ? Direct Presence Of Parent Companyin India (Not Only Through The Distributors ) And Company Must Provide Its Trained Technical Person For Each Implantation When Ever Required And Forfollow Up Programming When It Is Required ? Company Must Provide At Least One Programmer Exclusively To The Cardiology Dept. ?Company Must Quote Only The Latest Model Of Devices Commercially Available , Us Fda/Ce Approved, Vvi Permanent Pacemaker Without Lead ? Vvi ? All Single Chamber Modes And Basic Pacingprogrammable Parameters ? Should Have All Parameters Shown In Related Group Of Pacemaker ? Life Term Replacement Warranty ? Direct Presence Of Parent Companyin India (Not Only Through The Distributors ) And Company Must Provide Its Trained Technical Person For Each Implantation When Ever Required And Forfollow Up Programming When It Is Required ? Company Must Provide At Least One Programmer Exclusively To The Cardiology Dept. ? Company Must Quote Only The Latest Model Of Devices Commercially Available , Dcgiapproved, Vvi Permanent Pacemaker Without Lead ? Vvi ? All Single Chamber Modes And Basic Pacingprogrammable Parameters ? Should Have All Parameters Shown In Related Group Of Pacemaker ? Life Term Replacement Warranty ? Direct Presence Of Parent Companyin India (Not Only Through The Distributors ) And Company Must Provide Its Trained Technical Person For Each Implantation When Ever Required And Forfollow Up Programming When It Is Required ? Company Must Provide At Least One Programmer Exclusively To The Cardiology Dept. ? Company Must Quote Only The Latest Model Of Devices Commercially Available , Us Fda/Ce Approved, Vvirpermanent Pacemaker Without Lead ? Vvir ? All Single Chamber Modes And Basic Pacingprogrammable Parameters ? Should Have All Parameters Shown In Related Group Of Pacemaker ? Life Term Replacement Warranty ? Direct Presence Of Parent Companyin India (Not Only Through The Distributors ) And Company Must Provide Its Trained Technical Person For Each Implantation When Ever Required And Forfollow Up Programming When It Is Required ? Company Must Provide At Least One Programmer Exclusively To The Cardiology Dept. ? Company Must Quote Only The Latest Model Of Devices Commercially Available , Dcgiapproved, Vvirpermanent Pacemaker Without Lead Vvir ? All Single Chamber Modes And Basic Pacingprogrammable Parameters ? Should Have All Parameters Shown In Related Group Of Pacemaker ? Life Term Replacement Warranty ? Direct Presence Of Parent Companyin India (Not Only Through The Distributors ) And Company Must Provide Its Trained Technical Person For Each Implantation When Ever Required And Forfollow Up Programming When It Is Required ? Company Must Provide At Least One Programmer Exclusively To The Cardiology Dept. ? Company Must Quote Only The Latest Model Of Devices Commercially Available , Us Fda/Ce Approved, Vvirpermanent Pacemaker Without Lead ? Dddr ? Mri Compatible ? Life Term Replacement Warranty ? Direct Presence Of Parent Companyin India (Not Only Through The Distributors ) And Company Must Provide Its Trained Technical Person For Each Implantation When Ever Required And Forfollow Up Programming When It Is Required ? Company Must Provide At Least One Programmer Exclusively To The Cardiology Dept. ? Company Must Quote Only The Latest Model Of Devices Commercially Available , Dcgiapproved, Vvirpermanent Pacemaker Without Lead ?Dddr ? Mri Compatible ? Life Term Replacement Warranty ? Direct Presence Of Parent Companyin India (Not Only Through The Distributors ) And Company Must Provide Its Trained Technical Person For Each Implantation When Ever Required And Forfollow Up Programming When It Is Required ? Company Must Provide At Least One Programmer Exclusively To The Cardiology Dept. ? Company Must Quote Only The Latest Model Of Devices Commercially Available , Us Fda/Ce Approved, Atrial, Rv. Lv Leads And All Accessories For Biventricular Pacemaker (Crt) A Atrial Lead B Rv Lead C Lv Lead Should Have All Parameters Shown In Related Group Of Pacemaker Direct Presence Of Parent Companyin India (Not Only Through The Distributors ) And Company Must Provide Its Trained Technical Person For Each Implantation When Ever Required And Forfollow Up Programming When It Is Required Company Must Provide At Least One Programmer Exclusively To The Cardiology Dept. Company Must Quote Only The Latest Model Of Devices Commercially Available , Dcgi Approved, Atrial, Rv. Lv Leads And All Accessories For Biventricular Pacemaker (Crt) ? A Atrial Lead ? B Rv Lead ? C Lv Lead ? Should Have All Parameters Shown In Related Group Of Pacemaker ? Direct Presence Of Parent Companyin India (Not Only Through The Distributors ) And Company Must Provide Its Trained Technical Person For Each Implantation When Ever Required And Forfollow Up Programming When It Is Required ? Company Must Provide At Least One Programmer Exclusively To The Cardiology Dept. ? Company Must Quote Only The Latest Model Of Devices Commercially Available , Us Fda/Ce Approved, Rv Lead For Aicd Single Chamber ? Must Have All Specifications Shown In Related Group Of Pacemaker ? Rv Lead For Aicd Single Chamber ? Direct Presence Of Parent Companyin India (Not Only Through The Distributors ) And Company Must Provide Its Trained Technical Person For Each Implantation When Ever Required And Forfollow Up Programming When It Is Required ? Company Must Provide At Least One Programmer Exclusively To The Cardiology Dept. , Dcgiapproved, Rv Lead For Aicd Single Chamber ? Must Have All Specifications Shown In Related Group Of Pacemaker ? Rv Lead For Aicd Single Chamber ? Direct Presence Of Parent Companyin India (Not Only Through The Distributors ) And Company Must Provide Its Trained Technical Person For Each Implantation When Ever Required And Forfollow Up Programming When It Is Required ? Company Must Provide At Least One Programmer Exclusively To The Cardiology Dept. ? Company Must Quote Only The Latest Model Of Devices Commercially Available , Us Fda/Ce Approved, Pacing Leads For Aicd Dualchamber ? Must Have All Specifications Shown In Related Group Of Pacemaker ? Direct Presence Of Parent Companyin India (Not Only Through The Distributors ) And Company Must Provide Its Trained Technical Person For Each Implantation When Ever Required And Forfollow Up Programming When It Is Required ? Company Must Provide At Least One Programmer Exclusively To The Cardiology Dept. Company Must Quote Only The Latest Model Of Devices Commercially Available , Dcgiapproved, Pacing Leads For Aicd Dualchamber ? Must Have All Specifications Shown In Related Group Of Pacemaker ? Direct Presence Of Parent Companyin India (Not Only Through The Distributors ) And Company Must Provide Its Trained Technical Person For Each Implantation When Ever Required And Forfollow Up Programming When It Is Required ? Company Must Provide At Least One Programmer Exclusively To The Cardiology Dept. ? Company Must Quote Only The Latest Model Of Devices Commercially Available , Us Fda/Ce Approved, Pacing Lead (Atrial And Ventricular) For Dddr Permanent Pacemaker Aatrial Lead Bventricular Lead ? Must Have All Specifications Shown In Related Group Of Pacemaker ? Direct Presence Of Parent Companyin India (Not Only Through The Distributors ) And Company Must Provide Its Trained Technical Person For Each Implantation When Ever Required And Forfollow Up Programming When It Is Required ? Company Must Provide At Least One Programmer Exclusively To The Cardiology Dept. Company Must Quote Only The Latest Model Of Devices Commercially Available. Company Must Quote Only The Latest Model Of Devices Commercially Available , Dcgiapproved, Pacing Lead (Atrial And Ventricular) For Dddr Permanent Pacemaker Aatrial Lead Bventricular Lead ? Must Have All Specifications Shown In Related Group Of Pacemaker ? Direct Presence Of Parent Companyin India (Not Only Through The Distributors ) And Company Must Provide Its Trained Technical Person For Each Implantation When Ever Required And Forfollow Up Programming When It Is Required ? Company Must Provide At Least One Programmer Exclusively To The Cardiology Dept. ? Company Must Quote Only The Latest Model Of Devices Commercially Available , Us Fda/Ce Approved, Pacing Lead (Atrial And Ventricular) For Ddd Permanent Pacemakera Aatrial Lead Bventricular Lead ? Must Have All Specifications Shown In Related Group Of Pacemaker ? Direct Presence Of Parent Companyin India (Not Only Through The Distributors ) And Company Must Provide Its Trained Technical Person For Each Implantation When Ever Required And Forfollow Up Programming When It Is Required ? Company Must Provide At Least One Programmer Exclusively To The Cardiology Dept. ? Company Must Quote Only The Latest Model Of Devices Commercially Available , Dcgiapproved, Pacing Lead (Atrial And Ventricular) For Ddd Permanent Pacemaker Aatrial Lead Bventricular Lead ? Must Have All Specifications Shown In Related Group Of Pacemaker ? Direct Presence Of Parent Companyin India (Not Only Through The Distributors ) And Company Must Provide Its Trained Technical Person For Each Implantation When Ever Required And Forfollow Up Programming When It Is Required ? Company Must Provide At Least One Programmer Exclusively To The Cardiology Dept. ? Company Must Quote Only The Latest Model Of Devices Commercially Available , Us Fda/Ce Approved, Pacing Leads For Vdd/Vddr Pacemakers Must Have All Specifications Shown In Related Group Of Pacemaker ? Direct Presence Of Parent Companyin India (Not Only Through The Distributors ) And Company Must Provide Its Trained Technical Person For Each Implantation When Ever Required And Forfollow Up Programming When It Is Required ? Company Must Provide At Least One Programmer Exclusively To The Cardiology Dept. Company Must Quote Only The Latest Model Of Devices Commercially Available , Dcgiapproved, Pacing Leads For Vdd/Vddr Pacemakers ? Must Have All Specifications Shown In Related Group Of Pacemaker ? Direct Presence Of Parent Companyin India (Not Only Through The Distributors ) And Company Must Provide Its Trained Technical Person For Each Implantation When Ever Required And Forfollow Up Programming When It Is Required ? Company Must Provide At Least One Programmer Exclusively To The Cardiology Dept. ? Company Must Quote Only The Latest Model Of Devices Commercially Available , Usfda/Ceapproved, Pacing Leads For Vvi/Vvir Pacemakers ? Must Have All Specifications Shown In Related Group Of Pacemaker ? Direct Presence Of Parent Companyin India (Not Only Through The Distributors ) And Company Must Provide Its Trained Technical Person For Each Implantation When Ever Required And Forfollow Up Programming When It Is Required ? Company Must Provide At Least One Programmer Exclusively To The Cardiology Dept. Company Must Quote Only The Latest Model Of Devices Commercially Available. , Dcgiapproved, Pacing Leads For Vvi/Vvir Pacemakers ? Must Have All Specifications Shown In Related Group Of Pacemaker ? Direct Presence Of Parent Companyin India (Not Only Through The Distributors ) And Company Must Provide Its Trained Technical Person For Each Implantation When Ever Required And Forfollow Up Programming When It Is Required ? Company Must Provide At Least One Programmer Exclusively To The Cardiology Dept. ? Company Must Quote Only The Latest Model Of Devices Commercially Available. , Lead For Dddr Pacemaker – Ra Lead -Dcgi&Us Fda/ Ce Approved , Lead For Dddr Pacemaker – Ra Lead -Dcgi&Us Fda/ Ce Approved , Lead For Dddr Pacemaker – Rv Lead -Dcgi&Us Fda/ Ce Approved , Lead For Ddd Pacemaker – Ra Lead - Dcgi&Us Fda/ Ce Approved , Lead For Dddr Pacemaker – Rv Lead - Dcgi&Us Fda/ Ce Approved , Lead For Vdd Pacemaker – Dcgi Approved & Us Fda/ Ce Approved , Lead For Icdpacemaker – Dcgi & Us Fda/ Ce Approved , Lead For Icddual Chamberpacemaker - Dcgi&Us Fda/ Ce Approved , Lead For Crtpacemaker –Ra Lead Dcgi&Us Fda/ Ce Approved , Lead For Crtpacemaker –Rv Lead Dcgi&Us Fda/ Ce Approved , Lead For Crtpacemaker –Lvlead Dcgi&Us Fda/ Ce Approved , Lead For Crtdpacemaker –Rvlead Dcgi&Us Fda/ Ce Approved , Lead For Crtdpacemaker –Ralead Dcgi&Us Fda/ Ce Approved , Lead For Crtdpacemaker –Lvlead -Dcgi&Us Fda/ Ce Approved , Epicardial Pacing Lead – Rv Lead , Epicardial Pacing Lead – Ra Lead , Latex Surgical Gloves (Powdered) – Thickness -0.135 Mm • Natural Rubber Latex , Beaded Cuff, Protein Content Level: <200?G/Dm2 (As Per Astm D 5712) • Size – 6. 6.5, 7, 7.5, 8 , Latex Surgical Gloves (Powder Free) – Thickness -0.135 Mm • Natural Rubber Latex , Beaded Cuff, Protein Content Level: <50?G/Dm2 (As Per Astm D 5712) • Size – 6. 6.5, 7, 7.5, 8 , Silicon Coated Directly Jointed Sus & Sitinol Shaft Wire 0.7 Gm, Duo Core Technology – Ce Approved , Silicon Coated Directly Jointed Sus & Sitinol Shaft Wire – 0.7 Gm - Duo Core Technology Dcgi Approved , Silicon Coated Directly Jointed Sus & Sitinol Shaft Intermediate Wire 1 Gm,Duo Core Technology – Ce Approved , Silicon Coated Directly Jointed Sus & Sitinol Shaft Intermediate Wire – 1 Gm -Duo Core Technology Dcgi Approved , Stainless Steel Grinded, Core Wire,One Core Construction,Platinum Tip (3 Cm)- 195 Cm,Standard / 1.2 Gf, Intermediate / 1.0 Gf, Floppy / 0.8 Gf, Extra Floppy / 0.6 Gf – Ce Approved , Stainless Steel Grinded, Core Wire,One Core Construction,Platinum Tip (3 Cm)- 195 Cm,Standard / 1.2 Gf, Intermediate / 1.0 Gf Floppy / 0.8 Gf, Extra Floppy / 0.6 Gf – Dcgi Approved , Nitinol Distal Core Wire -Unicore- Both Nitinol - Le And Multiple Stainless-Steel Conjugation - Ultra-Low (<0.7 G) – 3-6 Gm Cto Wire - Ce Approved , Nitinol Distal Core Wire – Unicore -Both Nitinol - Le And Multiple Stainless-Steel Conjugation - Ultra-Low (<0.7 G) – 3-6 Gm Cto Wire - Dcgi Approved , Controlled Vascular Lumen Expansion Regulator System – Ce Approved , Controlled Vascular Lumen Expansion Regulator System – Dcgi Approved , Post Vascular Intervention Coronary Cvi-Balloon Catheters - Semi Crystalline Polymer Pressure Limit – 14-20 , Pre Vascular Intervention Coronary Cvi-Balloon Catheters - Semi Crystalline Co-Polymer Eft Shaft Pressure Limit – 7-14 , Vascular Intervention Coronary Cvi Drug-Coated Balloon -Lux Coating Technologyblends Paclitaxel With Bthc , Group – B (Interventional Neurology) , Disposable Luer Lock Syringe • Should Be Compitable With Cuanoacrylate. • Should Be Available In 1 C.C/2C.C/3C.C/5C.C/10 C.C/20 C.C/ 50C.C , Picard Catheter • In Various Standard Lengths And Curves • 035-038 Compatible 100 Cm Long , Amplatz Catheter : • In Various Standard Lengths And Curves • 035-038 Compatible 100 Cm Long , Carotid Angiopalsty Balloon Catheter(Over The Wire/Rapid Exchange) • Should Have Hydrophilic Coating • Should Be Available In Various Outer Diameters And Balloon Lengths And Various Shaft Lengths , Carotid Self Expendable Stents • Should Be 0.018” Compatible • Should Be Over The Wire And Rapid Exchange (Otw/Rx) • Should Be Available In Various Diameters And Length • Should Be On A Shaft Length Of 80-140 Or Above Length , Poly Vinyl Alcohol (Pva) Particles For Pre-Operative Tumour Embolization , Ethyl Vinyl Alcohol Embolic Agent (With Dmso) For Avms/Avfs/Davfs/Tumor-Embolization , Super Selective High Flow Infusion Catheters - For Cerebral/ Spinal Avms (Compitable With Dmso) Outer Diameter 2.7/1.5F, Distal Id- 0.013”, Usable Length At Least 165 Cm, , Super Selective High Flow Infusion Catheters - For Cerebral/ Spinal Avms (Compitable With Particulate Embolic Agents Such As Pva Particles) , Distal Acess Catheter For Co-Axial Systems • In Various Standerd Length • Size5fr 6Fr 7Fr • 0.035 To 0.070, 0.074 Inner Lumen , Baloon Topped Guiding Catheter • Size 6Fr 7Fr 8Fr 9Fr 10Rf , Special Micro Guidwire With Torque Device For Use With Micro Catheters • Size 0.007” – 0.014” , Special Micro Guidwire (Exchange Length 260-300Cm)With Torque Device For Use With Micro Catheterssize 0.010” – 0.014” , Electrolyte Detachable 3-D Type / Halical / 360 Coils For Intracranial Aneurysm Treatment – Bare Platinum Coils , Electrolyte Detachable 3-D Type / Halical / 360 Coils For Intracranial Aneurysm Treatment – Coated / Bio Active Platinum Coils , Selective Infusion Microcatheter For Intrecranial Aneurysm Treatment With 2 Tip Markers • Outer Diameter 2.1/1.7F And Id. 0.017” , Selective Infusion Microcatheter For Deploynig Intracranial Device Should Be Compitable For Stents Flow Diverters Or Stent Retrivers Of Various Sizes , Power Supply Acessiries And Connecting Cables For Detachable Coils , Open Cell Design Intracranial Stents For Stent Assisted Coilling Of Aneurysn • Should Have Open Cell Design • Should Be Available In Various Size And Diameter , Flow Diverter For Intracranial Aneurism Treatment , Single Lumen Baloon Angioplasty Catheter For Intrecranial Use , Hybrid Cell Design Intracranial Stents For Sten Assisted Coilleng Of Aneurusm • Should Have Open Cell Design • Should Be Available In Various Size And Diameter , Revasculization Device For Mechenical Thrombectomy , Thrombus Suction Catheters For Clot Retrivals From Carotid And Vertibtals , Infusion Catheter For Moterised Fragmentation And Suction For Clot Retrival With Seperater , Stent Retrival For Thrombectomy , Web Device Intraspecular – Available Assorted Size , Pressure Saline Bag 1000Ml , Pressure Infusion Reusable Bag 1000Ml
