Tender For Supply Of Cardiology Consumable And Implants At Rims, Ranchi, ranchi-Jharkhand

Supply Of Cardiology Consumable And Implants At Rims, Ranchi , List Of Of Cardiac & Other Instruments / Accessories / Consumables On Rate Contract Basis For Ayushmann Bharat Pmjay Scheme , 1. Coronary Guiding Catheter For Engagement Of Selective Coronary Ostium , A. Ptca Guiding Catheters :- It Should Be Large Lumen, Stainless Steel Braided, Inner Layer Coated With Pife. It Should Have Soft Tip With Radiopaque Marker Band At Tip For Femoral And Radial Route. 6F & 7F With Curves (3,3.5,4,5) Usfda Approved. Various Curves Like Judkins Left, Judkins Right, Al-1, Al-2, Ar-1, Ar-2, Ebu, Xb, Voda Left, Voda Right Or Other Similar Curves For Selective Engagement Of Right And Left Coronary Ostia To Be Provided. , B. Ptca Guiding Catheters :- It Should Be Large Lumen, Stainless Steel Braided, Inner Layer Coated With Pife. It Should Have Soft Tip With Radiopaque Marker Band At Tip For Femoral And Radial Route. 6F & 7F With Curves (3,3.5,4,5) Ce Approved . Various Curves Like Judkins Left, Judkins Right, Al-1,Al-2, Ar-1, Ar-2, Ebu, Xb, Voda Left, Voda Right Or Other Similar Curves For Selective Engagement Of Right And Left Coronary Ostia To Be Provided. , C. Ptca Guiding Catheters :- It Should Be Large Lumen, Stainless Steel Braided, Inner Layer Coated With Pife. It Should Have Soft Tip With Radiopaque Marker Band At Tip For Femoral And Radial Route. 6F & 7F With Curves (3,3.5,4,5) Dcgi Approved. Various Curves Like Judkins Left, Judkins Right, Al-1,Al-2, Ar-1, Ar-2, Ebu, Xb, Voda Left, Voda Right Or Other Similar Curves For Selective Engagement Of Right And Left Coronary Ostia To Be Provided. , 2. Coronary Diagnostic Catheter For Engagement Of Selective Coronary Ostium. , A. Tiger Catheter, Jl, Jr Or Similar Curves From Other Manufacturers. Guide Catheters To Be Provided In 5Fr Size. It Should Be Usfda Approved. , B. Tiger Catheter, Jl, Jr Or Similar Curves From Other Manufacturers. Guide Catheters To Be Provided In 5Fr Size. It Should Be Ce Approved . , C. Tiger Catheter, Jl, Jr Or Similar Curves From Other Manufacturers. Guide Catheters To Be Provided In 5Fr Size. It Should Be Dcgi Approved. , 3. Ptca Guidewire Hydrophilic , A. Steerable Ptca Wire With Hydrophilic Coating, 0.014 Floppy Tip With Extra Support 0.014. Usfda Approved , B. Steerable Ptca Wire With Hydrophilic Coating, 0.014 Floppy Tip With Extra Support 0.014. Ce Approved , C. Steerable Ptca Wire With Hydrophilic Coating, 0.014 Floppy Tip With Extra Support 0.014. Dcgi Approved , 4. Ptca Guidewire Extra Support , A. Steerable Ptca Wire With Extra Support, 0.014 Floppy Tip With Extra Support 0.014. Usfda Approved , B. Steerable Ptca Wire With Extra Support, 0.014 Floppy Tip With Extra Support 0.014. Ce Approved , C. Steerable Ptca Wire With Extra Support, 0.014 Floppy Tip With Extra Support 0.014. Dcgi Approved , 5. 014 Cornonary Guidewires Of Standard Length 175 To 190 Cm, Guide Wires With Tip Load < 1 Gram , A. Usfda Approved , B. Ce Approved , C. Dcgi Approved , 6. 014 Cornonary Guidewires Of Standard Length 175 To 190 Cm, Guide Wires With Tip Load 1-3 Gram , A. Usfda Approved , B. Ce Approved , C. Dcgi Approved , 7. 014 Cornonary Guidewires Of Standard Length 175 To 190 Cm, Guide Wires With Tip Load >3 Gram , A. Usfda Approved , B. Ce Approved , C. Dcgi Approved , 8. Drug Eluting Stents Of Various Diameters (All Available Diameter Sizes) And Various Lengths (All Available Lengths As Per Manufacturers) With The Following Specifications , A. 014 Ptca Gudewire Compatible. Monorail Design. Everolimus Eluting. Strut Thickness < 100 Um. Cocr Based Strut Design. Usfda Approved. , B. 014 Ptca Gudewire Compatible. Monorail Design. Sirolimus Eluting. Strut Thickness < 100 Um. Cocr Based Strut Design. Usfda Approved. , C. 014 Ptca Gudewire Compatible. Monorail Design. Zotarolimus Eluting. Strut Thickness < 100 Um. Cocr Based Strut Design. Usfda Approved. , D. 014 Ptca Gudewire Compatible. Monorail Design. Biolimus A9 Eluting. Strut Thickness < 100 Um. Cocr Based Strut Design. Usfda Approved. , E. 014 Ptca Gudewire Compatible. Monorail Design. Everolimus Eluting. Strut Thickness < 100 Um. Ptcr Based Strut Design. Usfda Approved. , F. 014 Ptca Gudewire Compatible. Monorail Design. Sirolimus Eluting. Strut Thickness < 100 Um. Ptcr Based Strut Design. Usfda Approved. , G. 014 Ptca Gudewire Compatible. Monorail Design. Zotarolimus Eluting. Strut Thickness < 100 Um. Ptcr Based Strut Design. Usfda Approved. , H. 014 Ptca Gudewire Compatible. Monorail Design. Biolimus A9 Eluting. Strut Thickness < 100 Um. Ptcr Based Strut Design. Usfda Approved. , I. 014 Ptca Gudewire Compatible. Monorail Design. Everolimus Eluting. Strut Thickness < 100 Um. Cocr Based Strut Design. Ce Approved. , J. 014 Ptca Gudewire Compatible. Monorail Design. Sirolimus Eluting. Strut Thickness < 100 Um. Cocr Based Strut Design. Ce Approved. , K. 014 Ptca Gudewire Compatible. Monorail Design. Zotarolimus Eluting. Strut Thickness < 100 Um. Cocr Based Strut Design. Ce Approved. , L. 014 Ptca Gudewire Compatible. Monorail Design. Biolimus A9 Eluting. Strut Thickness < 100 Um. Cocr Based Strut Design. Ce Approved. , M. 014 Ptca Gudewire Compatible. Monorail Design. Everolimus Eluting. Strut Thickness < 100 Um. Ptcr Based Strut Design. Ce Approved. , N. 014 Ptca Gudewire Compatible. Monorail Design. Sirolimus Eluting. Strut Thickness < 100 Um. Ptcr Based Strut Design. Ce Approved. , O. 014 Ptca Gudewire Compatible. Monorail Design. Zotarolimus Eluting. Strut Thickness < 100 Um. Ptcr Based Strut Design. Ce Approved. , P. 014 Ptca Gudewire Compatible. Monorail Design. Biolimus A9 Eluting. Strut Thickness < 100 Um. Ptcr Based Strut Design. Ce Approved. , Q. 014 Ptca Gudewire Compatible. Monorail Design. Everolimus Eluting. Strut Thickness < 100 Um. Cocr Based Strut Design. Dcgi Approved. , R. 014 Ptca Gudewire Compatible. Monorail Design. Sirolimus Eluting. Strut Thickness < 100 Um. Cocr Based Strut Design. Dcgi Approved. , S. 014 Ptca Gudewire Compatible. Monorail Design. Zotarolimus Eluting. Strut Thickness < 100 Um. Cocr Based Strut Design. Dcgi Approved. , T. 014 Ptca Gudewire Compatible. Monorail Design. Biolimus A9 Eluting. Strut Thickness < 100 Um. Cocr Based Strut Design. Dcgi Approved. , U. 014 Ptca Gudewire Compatible. Monorail Design. Everolimus Eluting. Strut Thickness < 100 Um. Ptcr Based Strut Design. Dcgi Approved. , V. 014 Ptca Gudewire Compatible. Monorail Design. Sirolimus Eluting. Strut Thickness < 100 Um. Ptcr Based Strut Design. Dcgi Approved. , W. 014 Ptca Gudewire Compatible. Monorail Design. Zotarolimus Eluting. Strut Thickness < 100 Um. Ptcr Based Strut Design. Dcgi Approved. , X. 014 Ptca Gudewire Compatible. Monorail Design. Biolimus A9 Eluting. Strut Thickness < 100 Um. Ptcr Based Strut Design. Dcgi Approved. , 9. 035 Ptfe Coronary Catheter Guidewire J Tip 145 To 170 Cm , 10. Pressure Monitoring Line 200 Cm Male To Female , 11. High Pressure Line Male To Female 120 Cm With Braided Tubing With Maximum Pressure Delivery Of 1200 Psi , 12. Ptca Kit With Y Connector, Tuohy Borst Valve And 25 Cm Extension Containing Torquer For Ptca Wire And Ptca Wire Insetion Tool , 13. Indeflator For Coronary Angioplasy With Maximum Pressure Capacity Of 30 Atm. , 14. Coronary Pre Dilatation Balloon Catheter For Coronary Angioplasty With Following Specifications. 014 Ptca Wire Compatible. Monorail Design. , A. Ptca Predilatation Monorail Balloon (Semi Complaint). Hypotube Shaft Design, Low Entry Profile (0.017) And Sequential Tip For Lesion Accessibility And Sf Guiding Catheter Compatibility. Diameter (In Mm):-1.5, 2.0, 2.5, 2.75, 3, 3.5 Length:- 10Mm To 20Mm And 1.25, 1.5 Mm Diameter Of <10 Mm Length. Usfda Approved , B. Ptca Predilatation Monorail Balloon (Semi Complaint). Hypotube Shaft Design, Low Entry Profile (0.017) And Sequential Tip For Lesion Accessibility And Sf Guiding Catheter Compatibility. Diameter (In Mm):- 1.5, 2.0, 2.5, 2.75, 3, 3.5 Length:- 10Mm To 20Mm And 1.25, 1.5 Mm Diameter Of <10 Mm Length. Ce Approved , C. Ptca Predilatation Monorail Balloon (Semi Complaint). Hypotube Shaft Design, Low Entry Profile (0.017) And Sequential Tip For Lesion Accessibility And Sf Guiding Catheter Compatibility. Diameter (In Mm):- 1.5, 2.0, 2.5, 2.75, 3, 3.5. Length:- 10Mm To 20Mm And 1.25, 1.5 Mm Diameter Of <10 Mm Length. Dcgi Approved , 15. Coronary Post Dilatation Balloon Catheter For Coronary Angioplasty With Following Specifications. 014 Ptca Wire Compatible. Monorail Design. , A. High Pressure Noncomplaint Balloon With High Rbp(20Atm Or More) Smooth, Rounded Distal Tip And No Edge. Overdialation At Higher Pressure, With Leart Balloon Overhang At The Edges Will Be Preferred. Diameter:- (Mm) - 2.5,2.75,3, 3.5, 4, 4.5. Length:- (Mm)- 8Mm To 20Mm. Usfda Approved , B. High Pressure Noncomplaint Balloon With High Rbp(20Atm Or More) Smooth, Rounded Distal Tip And No Edge. Overdialation At Higher Pressure, With Leart Balloon Overhang At The Edges Will Be Preferred. Diameter:- (Mm) - 2.5,2.75,3, 3.5, 4, 4.5. Length:- (Mm)- 8Mm To 20Mm. Ce Approved , C. High Pressure Noncomplaint Balloon With High Rbp(20Atm Or More) Smooth, Rounded Distal Tip And No Edge. Overdialation At Higher Pressure, With Leart Balloon Overhang At The Edges Will Be Preferred. Diameter:- (Mm) - 2.5,2.75,3, 3.5, 4, 4.5. Length:- (Mm)- 8Mm To 20Mm. Dcgi Approved , 16. Paclitaxel Coated Drug Eluting Coronary Balloon Of Carious Size Diameters And Lengths. , A. Usfda Approved , B. Ce Approved , C. Dcgi Approved , 17. Cutting Balloons For Coronary Angioplasty Of Various Diameter Sizes And Lengths. , A. Usfda Approved , B. Ce Approved , C. Dcgi Approved , 18. Pressure Monitoring Line 200 Cm Male To Female , 19. Vascular Sheath For Radial Artery Cannulation – 5 Fr, 6 Fr , A. Usfda Approved , B. Ce Approved , C. Dcgi Approved , 20. Vascular Sheath For Femoral Artery Cannulation – 6 Fr, 7 Fr, 8 Fr , A. Usfda Approved , B. Ce Approved , C. Dcgi Approved , 21. Temporary Pacing Wire 6Fr , A. Usfda Approved , B. Ce Approved , C. Dcgi Approved , A.Vvi Permanent Implantable Pacemaker • Us Fda Approved Pacemaker With Lead & Accessories. • All Single Chamber Modes And Basic Multi-Programmable Parameters With Preferably Autosensing And Auto Capture/Output Management Facilities. • Must Have Ventricular Capture Management. • Monitor The Integrity Of Lead And Switch Polarity In Case Of Issue • The Size Of Lead Should 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. • Company Must Provide At Least One Programmer Exclusively To The Department Of Cardiology Rims Ranchi. • Company Must Provide Its Trained Technical Person For Each Implantation And For Follow Up Programming Whenever Required. • Company Must Quote Only The Latest Model Of Devices Commercially Available. , 22.A .Vvir Permanent Implantable Pacemaker • Us Fda Approved Pacemaker With Lead & Accessories. • All Single Chamber Modes And Basic Multi-Programmable Parameters With Preferably Autosensing And Auto Capture/Output Management Facilities. • Must Have Ventricular Capture Management. • Monitor The Integrity Of Lead And Switch Polarity In Case Of Issue • The Size Of Lead Should 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. • Must Have Rate Response Which Allows Rate Profile Optimization. • Company Must Provide At Least One Programmer Exclusively To The Department Of Cardiology Rims Ranchi. • Company Must Provide Its Trained Technical Person For Each Implantation And For Follow Up Programming Whenever Required. • Company Must Quote Only The Latest Model Of Devices Commercially Available. , 22C .Ddd Permanent Implantable Pacemaker • Us Fda Approved Pacemaker With Lead & Accessories. • All Single/Dual Chamber Modes And Basic Multi-Programmable Parameters With Preferably Autosensing And Auto Capture/Output Management Facilities. • Must Have Ventricular/Atrial Capture Management. • Monitor The Integrity Of Lead And Switch Polarity In Case Of Issue • The Size Of Lead Should 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. • Company Must Provide At Least One Programmer Exclusively To The Department Of Cardiology Rims Ranchi. • Company Must Provide Its Trained Technical Person For Each Implantation And For Follow Up Programming Whenever Required. • Company Must Quote Only The Latest Model Of Devices Commercially Available. , 22D.Dddr Permanent Implantable Pacemaker • Us Fda Approved Pacemaker With Lead & Accessories. • All Single/Dual Chamber Modes And Basic Multi-Programmable Parameters With Preferably Autosensing And Auto Capture/Output Management Facilities. • Must Have Ventricular/Atrial Capture Management. • Monitor The Integrity Of Lead And Switch Polarity In Case Of Issue • The Size Of Lead Should 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. • Must Have Rate Response Which Allows Rate Profile Optimization. • Company Must Provide At Least One Programmer Exclusively To The Department Of Cardiology Rims Ranchi. • Company Must Provide Its Trained Technical Person For Each Implantation And For Follow Up Programming Whenever Required. • Company Must Quote Only The Latest Model Of Devices Commercially Available. , 22E Vvir Permanent Implantable Pacemaker Mri Compatiable • Us Fda Approved Pacemaker With Lead & Accessories. • All Single Chamber Modes And Basic Multi-Programmable Parameters With Preferably Autosensing And Auto Capture/Output Management Facilities. • Must Have Ventricular Capture Management. • Monitor The Integrity Of Lead And Switch Polarity In Case Of Issue • 3 Tesla Mri Compatible • The Size Of Lead Should 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. • Must Have Rate Response Which Allows Rate Profile Optimization. • Company Must Provide At Least One Programmer Exclusively To The Department Of Cardiology Rims Ranchi. • Company Must Provide Its Trained Technical Person For Each Implantation And For Follow Up Programming Whenever Required. • Company Must Quote Only The Latest Model Of Devices Commercially Available. , 22F Dddr Permanent Implantable Pacemaker • Us Fda Approved Pacemaker With Lead & Accessories. • All Single/Dual Chamber Modes And Basic Multi-Programmable Parameters With Preferably Autosensing And Auto Capture/Output Management Facilities. • Must Have Ventricular/Atrial Capture Management. • Monitor The Integrity Of Lead And Switch Polarity In Case Of Issue • 3 Tesla Mri Compatible • The Size Of Lead Should 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. • Must Have Rate Response Which Allows Rate Profile Optimization. • Company Must Provide At Least One Programmer Exclusively To The Department Of Cardiology Rims Ranchi. • Company Must Provide Its Trained Technical Person For Each Implantation And For Follow Up Programming Whenever Required. • Company Must Quote Only The Latest Model Of Devices Commercially Available. , 22G Icd Single Chamber • Us Fda Approved Icd , Small And Physiological Algorithm To Eliminate Over-Sensing Of R Wave, T Wave, Fractionated Qrs And Other Extraneous Signals Morphology Bases,Svt Discrimination Algoritm Atp During Charging Wireless Telemetry Encourage Intrinsic Conduction More Than 30 Minutes Of Stored Egm, A) Device With All Leads B) Device Without Leads Permanent Defibrillation Lead, Bipolar Endocardial Steroid Eluting Active And Passive Fixation Lead Company Must Provide At Least One Programmer Exclusively To The Department Of Cardiology Rims Ranchi. Company Must Provide Its Trained Technical Person For Each Implantation And For Follow Up Programming Whenever Required. Company Must Quote Only The Latest Model Of Devices Commercially Available. , 22H Icd Single Chamber Mri Compatiable- Specifications As Icd Single Chamber With Addition Of Mri Compatibility , 23.Double Lumen Balloon Dilatation Catheter Of Various Sizes For Percutaneous Transmitral Mitral Commisurotomy With All Accessories (Round Wire, Septal Dilator, J-Wire For Ptmc Balloon, Femoral Svenous Sheath) , 24.8 Fr Mullins Sheath For Trans-Septal Access , 25.32 Fe J Tipped Wire , 26.Transeptal Puncture Needle 70 Cm Long, Curved Tip, 18 Gauge With A Distal Taper To 21 Gauge, Preferably Brockenbrough Needle. , 27.Pigtail Cardiac Catheterisation Catheter 6 Fr , 28. Lbbb Area Dddr Permanent Implantable Pacemaker • Us Fda Approved Pacemaker With Lead & Accessories. • All Single/Dual Chamber Modes And Basic Multi-Programmable Parameters With Preferably Autosensing And Auto Capture/Output Management Facilities. • Must Have Ventricular/Atrial Capture Management. • Monitor The Integrity Of Lead And Switch Polarity In Case Of Issue • 3 Tesla Mri Compatible • The Size Of Lead Should Be 7F Or Less. • The Lead Must Be Configured For Implantation At Ra And Lbb Area. • Pre-Configured Sheath For Placement Of Lbb Area Lead To Be Provided • Must Have Both Active And Passive Fixation Endocardial Leads Available. • Must Have Rate Response Which Allows Rate Profile Optimization. • Company Should Provide Technical Assistance For Implantation And Programming. • Company Must Provide At Least One Programmer Exclusively To The Department Of Cardiology Rims Ranchi. • Company Must Provide Its Trained Technical Person For Each Implantation And For Follow Up Programming Whenever Required. • Company Must Quote Only The Latest Model Of Devices Commercially Available. , 29. Artificial Aortic Valve For Trans Catheter Placement (I) Transcatheter Heart Valve - 01 Unit It Should Be Made Of Bovine/Porcine Pericardium Tri Leaflet Valve, Made Of Medical Grade Alloy With Hybrid Cell Design .It Should Have Internal/Exteranl Pet Skirting Or Both. The Size Of The Valve Should Range From 20 Mm To 32 Mm Or More. (Ii) Valve Delivery System - 01 Unit The Valve Should Be Crimped Or Loaded Over The Delivery System Prior To Insertion Into The Patients Vasculature. Should Be 0.035 Wire Compatible (Iii) Balloon Dilatation Catheter - 01 Unit Balloon Size Ranges From 16 Mm To 25 Mm With 30 Mm Length. The Balloon Rbp Should Be Minimum 6 Atm. (Iv) Introducer Sheath 01 Unit Should Be Minimum 14 Fr And Length Of Minimum 30 Cm, Compatible With All Valve Sizes. Should Have Haemostatic Valve And Side Port With Three Way. Should Be Compatible For Femoral Artery Size Ranging From 5 Mm To 7 Mm. (V) Inflation Device - 02 Units (30Ml/40Ml/60Ml) (Vi) Syringes 50 Cc - 02 Units The Firm Should Be Able To Supply Any Size Of Valve, Delivery System And Balloon Suitable For The Patient. , 30. Electrophysiology Catheter 6F And 4 Mm Crd 2 Or 5Mm Electrode Spacing With Compatible Connector , 31. 7 French Quadripolar Radio Frequency Ablation Catheter With A 4 Mm Tip And Bidirectional Deflection. Should Be Available In Small, Medium And Large Curves. Should Be Compatible With The Available. , 32. 7 French Quadripolar Radio Frequency Ablation Catheter With A 4 Mm Tip And Unidirectional Deflection. Should Be Available In Small, Medium And Large Curves. Should Be Compatible With The Available , 33. 5 French Fixed Curve Quadripolar Catheter With 2-5-2 Interelectrode Spacing. One Matching Connector For Every 5 Catheters. Should Be Fda/Ce/Dcgi Approved , 34.6 French Deflectable Quadripolar Catheter With 2-5-2 Interelectrode Spacing And Matching Connector. Should Be Fda/Ce/Dcgi Approved , 35. 6 French Deflectable Decapolar Catheter With 2-5-2 Interelectrode Spacing And Matching Connector. Should Be Fda/Ce/Dcgi Approved . , 36. 6 Or 7 French Deflectable Duodecapolar Catheters (Halo) With Matching Connectors. Should Be Fda/Ce/Dcgi Approved , 37. Long Deflectable Sheath With Hemostatic Valve, Side Port, Atraumatic Tip, Braided Shaft, Uni- Or Bidirectional Steerability, Availability In Small, Medium Or Large Curves, Minimum Inner Diameter Or 7F, Minimum Length Of 65 Cms. Should Be Fda/Ce/Dcgi Approved , 38. 7 French Quadripolar Radiofrequency Ablation Catheter With A 4 Mm Tip, Unidirectional Deflection, Availability In Small, Medium And Large Curves. Should Be Compatible With Stockert And Ibi Rf Generators And Suitable Connecting Cable Should Be Provided For Every 5 Catheters.. Should Be Fda/Ce/Dcgi Approved , 39. 7 French Quadripolar Radiofrequency Ablation Catheter With A 4 Mm Tip, Bidirectional Deflection, Availability In Small, Medium And Large Curves. Should Be Compatible With Stockert And Ibi Rf Generators And Suitable Connecting Cables Should Be Provided . Should Be Fda/Ce/Dcgi Approved , 40. 7 French Quadripolar Radiofrequency Ablation Catheter With A 8 Mm Tip, Unidirectional Deflection, Availability In Medium And Large Curves. Should Be Compatible With Stockert And Ibi Rf Generators And Suitable Connecting Cable Should Be Provided For Every 5 Catheters.. Should Be Fda/Ce/Dcgi Approved , 41. 7 French Quadripolar Radiofrequency Ablation Catheter With Irrigated Tip, Uni- Or Bi-Directional Deflection And Availability In Medium And Large Curves. Should Be Compatible With Stockert And Ibi Rf Generators And Suitable Connecting Cable Should Be Provided For Every 5 Catheters.. Should Be Fda/Ce/Dcgi Approved , 42. Quadripolar, Irrigated Tip, Radiofrequency Ablation Catheter With A 3.5 Mm Tip And Unidirectional Deflection For Use With The Carto Mapping System. Should Include Irrigation Tubing Set For Interface Between The Irrigation Pump And The Ablation Catheter And Matching External Reference Patch For Use With The Carto 3 System. Should Be Fda/Ce/Dcgi Approved , 43. Crt - Triple Chamber Pacing System Comprising Pacemaker, Active Atrial And Ventricular Leads And Bipolar, Over The Wire Coronary Sinus Lead. Should Include Long Preshaped Slittable Sheaths For Coronary Sinus Cannulation In Multiple Shapes, Sub-Selective Inner Sheaths, Guidewire And Occlusion Balloon Catheter For Coronary Venography. Coronary Sinus Lead Should Be Available In Multiple Curves / Sizes.. Should Be Fda/Ce/Dcgi Approved , 44. Bipolar Lead Specially Designed For Placement In Coronary Sinus For Lv Pacing. Should Be Supplied With 9F Short Sheath With Valve, Long Pre-Shaped Slittable Sheaths In Various Shapes For Cs Cannulation And Inner Sub-Selective Sheath. Lead, Long Sheath, Sub-Selective Sheath And Short Sheath Should Be Quoted As One Set.. Should Be Fda/Ce/Dcgi Approved , 45. Embolization Coils 035 All Sizes. Should Be Fda/Ce/Dcgi Approved , 46. Embolization Micro Coils 018 All Sizes - Non Detachable And Freely Deliverable. Should Be Fda/Ce/Dcgi Approved , 47. Embolization Micro Coils 018 All Sizes -Detachable 2D. Should Be Fda/Ce/Dcgi Approved , 48. Embolisation Particles Poly Vinyl Alcohol All Sizes. Should Be Fda/Ce/Dcgi Approved , 49. Gelfoam (Powder Or Granule Form) For Embolization. Should Be Fda/Ce/Dcgi Approved , 50. Microcatheters With Inbuilt Hydrophilic Wire For Peripheral Angiography And Particle /Coil Delivery. Should Be Fda/Ce/Dcgi Approved , 51. Microcatheters - Steerable/ Shapable With Inbuilt Hydrophilic Wire For Peripheral Angiography And Particle /Coil Delivery. Should Be Fda/Ce/Dcgi Approved , 52. Soft Guideliner For Mother And Child Technique. Should Be Fda Or Ce And Dcgi Approved , 53. Rotablator Wire 009. Should Be Fda/Ce/Dcgi Approved , 54. Rotablator Advancer. Should Be Fda/Ce/Dcgi Approved , 55. Rotablator Burr. Should Be Fda/Ce/Dcgi Approved , 56. Asd Amplatzer Type Self Centre Devices With All Sizes From 8Mm And Above . Should Be Fda Approved , 57. Cook Sheaths (All Sizes 6F-15F) With Check Flo Valves) With Angled Tips For Asd Device Delivery. Should Be Fda Or Ce And Dcgi Approved , 58. Pda Occusion Device --All Customisable Sizes With From 3Mm To 20Mm Waist Size . Should Be Fda/Ce/Dcgi Approved , 59. Pda Delivery Systems And Introducer Cable Systems . Should Be Fda/Ce/Dcgi Approved , 60. Ventricular Septal Closure Devices All Sizes ( 4Mm To18 Mm). Should Be Fda/Ce/Dcgi Approved , 61. Delivery Cable And Sheath Set For Ventricular Septal Defect Closure. Should Be Fda Or Ce And Dcgi Approved

INR 5000 /-

INR 150000.0 /-

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Name of Work: < Supply of Consumable and Implant for the department of Cardiology, RIMS, Ranchi

Sl. No.	Item Description
1	LIST OF OF CARDIAC & OTHER INSTRUMENTS / ACCESSORIES / CONSUMABLES ON RATE CONTRACT BASIS FOR AYUSHMANN BHARAT PMJAY SCHEME
2	1. CORONARY GUIDING CATHETER FOR ENGAGEMENT OF SELECTIVE CORONARY OSTIUM
3	A. PTCA Guiding Catheters :- It should be large Lumen, stainless steel braided, inner layer coated with PIFE. It should have soft tip with radiopaque marker band at tip for femoral and radial route. 6F & 7F with curves (3,3.5,4,5) USFDA approved. Various curves like Judkins left, Judkins right, AL-1, AL-2, AR-1, AR-2, EBU, XB, Voda left, Voda right or other similar curves for selective engagement of right and left coronary ostia to be provided.
4	B. PTCA Guiding Catheters :- It should be large Lumen, stainless steel braided, inner layer coated with PIFE. It should have soft tip with radiopaque marker band at tip for femoral and radial route. 6F & 7F with curves (3,3.5,4,5) CE approved . Various curves like Judkins left, Judkins right, AL-1,AL-2, AR-1, AR-2, EBU, XB, Voda left, Voda right or other similar curves for selective engagement of right and left coronary ostia to be provided.
5	C. PTCA Guiding Catheters :- It should be large Lumen, stainless steel braided, inner layer coated with PIFE. It should have soft tip with radiopaque marker band at tip for femoral and radial route. 6F & 7F with curves (3,3.5,4,5) DCGI approved. Various curves like Judkins left, Judkins right, AL-1,AL-2, AR-1, AR-2, EBU, XB, Voda left, Voda right or other similar curves for selective engagement of right and left coronary ostia to be provided.
6	2. CORONARY DIAGNOSTIC CATHETER FOR ENGAGEMENT OF SELECTIVE CORONARY OSTIUM.
7	A. TIGER CATHETER, JL, JR OR SIMILAR CURVES FROM OTHER MANUFACTURERS. GUIDE CATHETERS TO BE PROVIDED IN 5FR SIZE. It should be USFDA approved.
8	B. TIGER CATHETER, JL, JR OR SIMILAR CURVES FROM OTHER MANUFACTURERS. GUIDE CATHETERS TO BE PROVIDED IN 5FR SIZE. It should be CE approved .
9	C. TIGER CATHETER, JL, JR OR SIMILAR CURVES FROM OTHER MANUFACTURERS. GUIDE CATHETERS TO BE PROVIDED IN 5FR SIZE. It should be DCGI approved.
10	3. PTCA GUIDEWIRE HYDROPHILIC
11	A. Steerable PTCA Wire with hydrophilic coating, 0.014" floppy tip with extra support 0.014". USFDA approved
12	B. Steerable PTCA Wire with hydrophilic coating, 0.014" floppy tip with extra support 0.014". CE approved
13	C. Steerable PTCA Wire with hydrophilic coating, 0.014" floppy tip with extra support 0.014". DCGI approved
14	4. PTCA GUIDEWIRE EXTRA SUPPORT
15	A. Steerable PTCA Wire with EXTRA SUPPORT, 0.014" floppy tip with extra support 0.014". USFDA approved
16	B. Steerable PTCA Wire with EXTRA SUPPORT, 0.014" floppy tip with extra support 0.014". CE approved
17	C. Steerable PTCA Wire with EXTRA SUPPORT, 0.014" floppy tip with extra support 0.014". DCGI approved
18	5. 014 CORNONARY GUIDEWIRES OF STANDARD LENGTH 175 TO 190 CM, GUIDE WIRES WITH TIP LOAD < 1 GRAM
19	A. USFDA APPROVED
20	B. CE APPROVED
21	C. DCGI APPROVED
22	6. 014 CORNONARY GUIDEWIRES OF STANDARD LENGTH 175 TO 190 CM, GUIDE WIRES WITH TIP LOAD 1-3 GRAM
23	A. USFDA APPROVED
24	B. CE APPROVED
25	C. DCGI APPROVED
26	7. 014 CORNONARY GUIDEWIRES OF STANDARD LENGTH 175 TO 190 CM, GUIDE WIRES WITH TIP LOAD >3 GRAM
27	A. USFDA APPROVED
28	B. CE APPROVED
29	C. DCGI APPROVED
30	8. DRUG ELUTING STENTS OF VARIOUS DIAMETERS (all available diameter sizes) AND VARIOUS LENGTHS (all available lengths as per manufacturers) WITH THE FOLLOWING SPECIFICATIONS
31	A. 014 PTCA GUDEWIRE COMPATIBLE. MONORAIL DESIGN. EVEROLIMUS ELUTING. STRUT THICKNESS < 100 UM. CoCr BASED STRUT DESIGN. USFDA approved.
32	B. 014 PTCA GUDEWIRE COMPATIBLE. MONORAIL DESIGN. SIROLIMUS ELUTING. STRUT THICKNESS < 100 UM. CoCr BASED STRUT DESIGN. USFDA approved.
33	C. 014 PTCA GUDEWIRE COMPATIBLE. MONORAIL DESIGN. ZOTAROLIMUS ELUTING. STRUT THICKNESS < 100 UM. CoCr BASED STRUT DESIGN. USFDA approved.
34	D. 014 PTCA GUDEWIRE COMPATIBLE. MONORAIL DESIGN. BIOLIMUS A9 ELUTING. STRUT THICKNESS < 100 UM. CoCr BASED STRUT DESIGN. USFDA approved.
35	E. 014 PTCA GUDEWIRE COMPATIBLE. MONORAIL DESIGN. EVEROLIMUS ELUTING. STRUT THICKNESS < 100 UM. PtCr BASED STRUT DESIGN. USFDA approved.
36	F. 014 PTCA GUDEWIRE COMPATIBLE. MONORAIL DESIGN. SIROLIMUS ELUTING. STRUT THICKNESS < 100 UM. PtCr BASED STRUT DESIGN. USFDA approved.
37	G. 014 PTCA GUDEWIRE COMPATIBLE. MONORAIL DESIGN. ZOTAROLIMUS ELUTING. STRUT THICKNESS < 100 UM. PtCr BASED STRUT DESIGN. USFDA approved.
38	H. 014 PTCA GUDEWIRE COMPATIBLE. MONORAIL DESIGN. BIOLIMUS A9 ELUTING. STRUT THICKNESS < 100 UM. PtCr BASED STRUT DESIGN. USFDA approved.
39	I. 014 PTCA GUDEWIRE COMPATIBLE. MONORAIL DESIGN. EVEROLIMUS ELUTING. STRUT THICKNESS < 100 UM. CoCr BASED STRUT DESIGN. CE approved.
40	J. 014 PTCA GUDEWIRE COMPATIBLE. MONORAIL DESIGN. SIROLIMUS ELUTING. STRUT THICKNESS < 100 UM. CoCr BASED STRUT DESIGN. CE approved.
41	K. 014 PTCA GUDEWIRE COMPATIBLE. MONORAIL DESIGN. ZOTAROLIMUS ELUTING. STRUT THICKNESS < 100 UM. CoCr BASED STRUT DESIGN. CE approved.
42	L. 014 PTCA GUDEWIRE COMPATIBLE. MONORAIL DESIGN. BIOLIMUS A9 ELUTING. STRUT THICKNESS < 100 UM. CoCr BASED STRUT DESIGN. CE approved.
43	M. 014 PTCA GUDEWIRE COMPATIBLE. MONORAIL DESIGN. EVEROLIMUS ELUTING. STRUT THICKNESS < 100 UM. PtCr BASED STRUT DESIGN. CE approved.
44	N. 014 PTCA GUDEWIRE COMPATIBLE. MONORAIL DESIGN. SIROLIMUS ELUTING. STRUT THICKNESS < 100 UM. PtCr BASED STRUT DESIGN. CE approved.
45	O. 014 PTCA GUDEWIRE COMPATIBLE. MONORAIL DESIGN. ZOTAROLIMUS ELUTING. STRUT THICKNESS < 100 UM. PtCr BASED STRUT DESIGN. CE approved.
46	P. 014 PTCA GUDEWIRE COMPATIBLE. MONORAIL DESIGN. BIOLIMUS A9 ELUTING. STRUT THICKNESS < 100 UM. PtCr BASED STRUT DESIGN. CE approved.
47	Q. 014 PTCA GUDEWIRE COMPATIBLE. MONORAIL DESIGN. EVEROLIMUS ELUTING. STRUT THICKNESS < 100 UM. CoCr BASED STRUT DESIGN. DCGI approved.
48	R. 014 PTCA GUDEWIRE COMPATIBLE. MONORAIL DESIGN. SIROLIMUS ELUTING. STRUT THICKNESS < 100 UM. CoCr BASED STRUT DESIGN. DCGI approved.
49	S. 014 PTCA GUDEWIRE COMPATIBLE. MONORAIL DESIGN. ZOTAROLIMUS ELUTING. STRUT THICKNESS < 100 UM. CoCr BASED STRUT DESIGN. DCGI approved.
50	T. 014 PTCA GUDEWIRE COMPATIBLE. MONORAIL DESIGN. BIOLIMUS A9 ELUTING. STRUT THICKNESS < 100 UM. CoCr BASED STRUT DESIGN. DCGI approved.
51	U. 014 PTCA GUDEWIRE COMPATIBLE. MONORAIL DESIGN. EVEROLIMUS ELUTING. STRUT THICKNESS < 100 UM. PtCr BASED STRUT DESIGN. DCGI approved.
52	V. 014 PTCA GUDEWIRE COMPATIBLE. MONORAIL DESIGN. SIROLIMUS ELUTING. STRUT THICKNESS < 100 UM. PtCr BASED STRUT DESIGN. DCGI approved.
53	W. 014 PTCA GUDEWIRE COMPATIBLE. MONORAIL DESIGN. ZOTAROLIMUS ELUTING. STRUT THICKNESS < 100 UM. PtCr BASED STRUT DESIGN. DCGI approved.
54	X. 014 PTCA GUDEWIRE COMPATIBLE. MONORAIL DESIGN. BIOLIMUS A9 ELUTING. STRUT THICKNESS < 100 UM. PtCr BASED STRUT DESIGN. DCGI approved.
55	9. 035 PTFE CORONARY CATHETER GUIDEWIRE J TIP 145 TO 170 CM
56	10. PRESSURE MONITORING LINE 200 CM MALE TO FEMALE
57	11. HIGH PRESSURE LINE MALE TO FEMALE 120 CM WITH BRAIDED TUBING WITH MAXIMUM PRESSURE DELIVERY OF 1200 Psi
58	12. PTCA KIT WITH Y CONNECTOR, TUOHY BORST VALVE AND 25 CM EXTENSION CONTAINING TORQUER FOR PTCA WIRE AND PTCA WIRE INSETION TOOL
59	13. INDEFLATOR FOR CORONARY ANGIOPLASY WITH MAXIMUM PRESSURE CAPACITY OF 30 ATM.
60	14. CORONARY PRE DILATATION BALLOON CATHETER FOR CORONARY ANGIOPLASTY WITH FOLLOWING SPECIFICATIONS. 014 PTCA WIRE COMPATIBLE. MONORAIL DESIGN.
61	A. PTCA predilatation monorail balloon (semi complaint). Hypotube shaft design, low entry profile (0.017") and sequential tip for lesion accessibility and SF guiding catheter compatibility. Diameter (in mm):-1.5, 2.0, 2.5, 2.75, 3, 3.5 Length:- 10mm to 20mm and 1.25, 1.5 mm diameter of <10 mm length. USFDA approved
62	B. PTCA predilatation monorail balloon (semi complaint). Hypotube shaft design, low entry profile (0.017") and sequential tip for lesion accessibility and SF guiding catheter compatibility. Diameter (in mm):- 1.5, 2.0, 2.5, 2.75, 3, 3.5 Length:- 10mm to 20mm and 1.25, 1.5 mm diameter of <10 mm length. CE approved
63	C. PTCA predilatation monorail balloon (semi complaint). Hypotube shaft design, low entry profile (0.017") and sequential tip for lesion accessibility and SF guiding catheter compatibility. Diameter (in mm):- 1.5, 2.0, 2.5, 2.75, 3, 3.5. Length:- 10mm to 20mm and 1.25, 1.5 mm diameter of <10 mm length. DCGI approved
64	15. CORONARY POST DILATATION BALLOON CATHETER FOR CORONARY ANGIOPLASTY WITH FOLLOWING SPECIFICATIONS. 014 PTCA WIRE COMPATIBLE. MONORAIL DESIGN.
65	A. High Pressure noncomplaint balloon with high RBP(20ATM or more) smooth, rounded distal tip and no edge. Overdialation at higher pressure, with leart balloon overhang at the edges will be preferred. Diameter:- (mm) - 2.5,2.75,3, 3.5, 4, 4.5. Length:- (mm)- 8mm to 20mm. USFDA approved
66	B. High Pressure noncomplaint balloon with high RBP(20ATM or more) smooth, rounded distal tip and no edge. Overdialation at higher pressure, with leart balloon overhang at the edges will be preferred. Diameter:- (mm) - 2.5,2.75,3, 3.5, 4, 4.5. Length:- (mm)- 8mm to 20mm. CE approved
67	C. High Pressure noncomplaint balloon with high RBP(20ATM or more) smooth, rounded distal tip and no edge. Overdialation at higher pressure, with leart balloon overhang at the edges will be preferred. Diameter:- (mm) - 2.5,2.75,3, 3.5, 4, 4.5. Length:- (mm)- 8mm to 20mm. DCGI approved
68	16. Paclitaxel coated drug eluting coronary balloon of carious size diameters and lengths.
69	A. USFDA approved
70	B. CE approved
71	C. DCGI approved
72	17. Cutting Balloons for coronary angioplasty of various diameter sizes and lengths.
73	A. USFDA approved
74	B. CE approved
75	C. DCGI approved
76	18. PRESSURE MONITORING LINE 200 CM MALE TO FEMALE
77	19. VASCULAR SHEATH FOR RADIAL ARTERY CANNULATION – 5 Fr, 6 Fr
78	a. USFDA approved
79	B. CE approved
80	C. DCGI approved
81	20. VASCULAR SHEATH FOR FEMORAL ARTERY CANNULATION – 6 Fr, 7 Fr, 8 Fr
82	a. USFDA approved
83	B. CE approved
84	C. DCGI approved
85	21. TEMPORARY PACING WIRE 6FR
86	a. USFDA approved
87	B. CE approved
88	C. DCGI approved
89	A.VVI PERMANENT IMPLANTABLE PACEMAKER • US FDA approved pacemaker with lead & accessories. • All single Chamber modes and basic multi-programmable parameters with preferably autosensing and auto capture/output management facilities. • Must have Ventricular Capture Management. • Monitor the integrity of lead and switch polarity in case of issue • The Size of lead should 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. • Company must provide at least one programmer exclusively to the department of cardiology RIMS Ranchi. • Company must provide its trained technical person for each implantation and for follow up programming whenever required. • Company must quote only the latest model of devices commercially available.
90	22.A .VVIR PERMANENT IMPLANTABLE PACEMAKER • US FDA approved pacemaker with lead & accessories. • All single Chamber modes and basic multi-programmable parameters with preferably autosensing and auto capture/output management facilities. • Must have Ventricular Capture Management. • Monitor the integrity of lead and switch polarity in case of issue • The Size of lead should 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. • Must have rate response which allows rate profile optimization. • Company must provide at least one programmer exclusively to the department of cardiology RIMS Ranchi. • Company must provide its trained technical person for each implantation and for follow up programming whenever required. • Company must quote only the latest model of devices commercially available.
91	22C .DDD PERMANENT IMPLANTABLE PACEMAKER • US FDA approved pacemaker with lead & accessories. • All single/Dual Chamber modes and basic multi-programmable parameters with preferably autosensing and auto capture/output management facilities. • Must have Ventricular/Atrial Capture Management. • Monitor the integrity of lead and switch polarity in case of issue • The Size of lead should 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. • Company must provide at least one programmer exclusively to the department of cardiology RIMS Ranchi. • Company must provide its trained technical person for each implantation and for follow up programming whenever required. • Company must quote only the latest model of devices commercially available.
92	22D.DDDR PERMANENT IMPLANTABLE PACEMAKER • US FDA approved pacemaker with lead & accessories. • All single/Dual Chamber modes and basic multi-programmable parameters with preferably autosensing and auto capture/output management facilities. • Must have Ventricular/Atrial Capture Management. • Monitor the integrity of lead and switch polarity in case of issue • The Size of lead should 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. • Must have rate response which allows rate profile optimization. • Company must provide at least one programmer exclusively to the department of cardiology RIMS Ranchi. • Company must provide its trained technical person for each implantation and for follow up programming whenever required. • Company must quote only the latest model of devices commercially available.
93	22E VVIR PERMANENT IMPLANTABLE PACEMAKER MRI COMPATIABLE • US FDA approved pacemaker with lead & accessories. • All single Chamber modes and basic multi-programmable parameters with preferably autosensing and auto capture/output management facilities. • Must have Ventricular Capture Management. • Monitor the integrity of lead and switch polarity in case of issue • 3 Tesla MRI Compatible • The Size of lead should 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. • Must have rate response which allows rate profile optimization. • Company must provide at least one programmer exclusively to the department of cardiology RIMS Ranchi. • Company must provide its trained technical person for each implantation and for follow up programming whenever required. • Company must quote only the latest model of devices commercially available.
94	22F DDDR PERMANENT IMPLANTABLE PACEMAKER • US FDA approved pacemaker with lead & accessories. • All single/Dual Chamber modes and basic multi-programmable parameters with preferably autosensing and auto capture/output management facilities. • Must have Ventricular/Atrial Capture Management. • Monitor the integrity of lead and switch polarity in case of issue • 3 Tesla MRI Compatible • The Size of lead should 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. • Must have rate response which allows rate profile optimization. • Company must provide at least one programmer exclusively to the department of cardiology RIMS Ranchi. • Company must provide its trained technical person for each implantation and for follow up programming whenever required. • Company must quote only the latest model of devices commercially available.
95	22G ICD SINGLE CHAMBER • US FDA approved ICD , small and physiological Algorithm to eliminate over-sensing of R wave, T wave, fractionated QRS and other extraneous signals morphology bases,SVT discrimination algoritm ATP during charging wireless telemetry encourage intrinsic conduction more than 30 minutes of stored EGM, a) Device with all leads b) device without leads Permanent defibrillation lead, bipolar endocardial steroid eluting active and passive fixation lead Company must provide at least one programmer exclusively to the department of cardiology RIMS Ranchi. Company must provide its trained technical person for each implantation and for follow up programming whenever required. Company must quote only the latest model of devices commercially available.
96	22H ICD SINGLE CHAMBER MRI COMPATIABLE- Specifications as ICD single chamber with addition of MRI compatibility
97	23.DOUBLE LUMEN BALLOON DILATATION CATHETER OF VARIOUS SIZES FOR PERCUTANEOUS TRANSMITRAL MITRAL COMMISUROTOMY WITH ALL ACCESSORIES (ROUND WIRE, SEPTAL DILATOR, J-WIRE FOR PTMC BALLOON, FEMORAL SVENOUS SHEATH)
98	24.8 FR MULLINS SHEATH FOR TRANS-SEPTAL ACCESS
99	25.32 FE J TIPPED WIRE
100	26.TRANSEPTAL PUNCTURE NEEDLE 70 CM LONG, CURVED TIP, 18 GAUGE WITH A DISTAL TAPER TO 21 GAUGE, PREFERABLY BROCKENBROUGH NEEDLE.
101	27.PIGTAIL CARDIAC CATHETERISATION CATHETER 6 FR
102	28. LBBB AREA DDDR PERMANENT IMPLANTABLE PACEMAKER • US FDA approved pacemaker with lead & accessories. • All single/Dual Chamber modes and basic multi-programmable parameters with preferably autosensing and auto capture/output management facilities. • Must have Ventricular/Atrial Capture Management. • Monitor the integrity of lead and switch polarity in case of issue • 3 Tesla MRI Compatible • The Size of lead should be 7F or less. • The Lead must be configured for implantation at RA and LBB area. • Pre-configured sheath for placement of LBB area lead to be provided • Must have both active and passive fixation endocardial leads available. • Must have rate response which allows rate profile optimization. • Company should provide technical assistance for implantation and programming. • Company must provide at least one programmer exclusively to the department of cardiology RIMS Ranchi. • Company must provide its trained technical person for each implantation and for follow up programming whenever required. • Company must quote only the latest model of devices commercially available.
103	29. Artificial aortic valve for trans catheter placement (i) TRANSCATHETER HEART VALVE - 01 UNIT IT SHOULD BE MADE OF BOVINE/PORCINE PERICARDIUM TRI LEAFLET VALVE, MADE OF MEDICAL GRADE ALLOY WITH HYBRID CELL DESIGN .IT SHOULD HAVE INTERNAL/EXTERANL PET SKIRTING OR BOTH. THE SIZE OF THE VALVE SHOULD RANGE FROM 20 MM TO 32 MM OR MORE. (ii) VALVE DELIVERY SYSTEM - 01 UNIT THE VALVE SHOULD BE CRIMPED OR LOADED OVER THE DELIVERY SYSTEM PRIOR TO INSERTION INTO THE PATIENTS VASCULATURE. SHOULD BE 0.035 WIRE COMPATIBLE (iii) BALLOON DILATATION CATHETER - 01 UNIT BALLOON SIZE RANGES FROM 16 MM TO 25 MM WITH 30 MM LENGTH. THE BALLOON RBP SHOULD BE MINIMUM 6 atm. (iv) INTRODUCER SHEATH 01 UNIT SHOULD BE MINIMUM 14 FR AND LENGTH OF MINIMUM 30 CM, COMPATIBLE WITH ALL VALVE SIZES. SHOULD HAVE HAEMOSTATIC VALVE AND SIDE PORT WITH THREE WAY. SHOULD BE COMPATIBLE FOR FEMORAL ARTERY SIZE RANGING FROM 5 MM TO 7 MM. (v) INFLATION DEVICE - 02 UNITS (30ML/40ML/60ML) (vi) SYRINGES 50 CC - 02 UNITS THE FIRM SHOULD BE ABLE TO SUPPLY ANY SIZE OF VALVE, DELIVERY SYSTEM AND BALLOON SUITABLE FOR THE PATIENT.
104	30. Electrophysiology Catheter 6F and 4 Mm Crd 2 or 5Mm Electrode Spacing with Compatible Connector
105	31. 7 French Quadripolar Radio Frequency Ablation Catheter with a 4 Mm Tip and Bidirectional Deflection. should be Available in Small, Medium and Large Curves. should be Compatible with the available.
106	32. 7 French Quadripolar Radio Frequency Ablation Catheter with a 4 Mm Tip and unidirectional Deflection. should be Available in Small, Medium and Large Curves. should be Compatible with the available
107	33. 5 French fixed curve quadripolar catheter with 2-5-2 interelectrode spacing. One matching connector for every 5 catheters. Should be FDA"/CE"/DCGI approved
108	34.6 French deflectable quadripolar catheter with 2-5-2 interelectrode spacing and matching connector. Should be FDA"/CE"/DCGI approved
109	35. 6 French deflectable decapolar catheter with 2-5-2 interelectrode spacing and matching connector. Should be FDA"/CE"/DCGI approved .
110	36. 6 or 7 French deflectable duodecapolar catheters (Halo) with matching connectors. Should be FDA"/CE"/DCGI approved
111	37. Long deflectable sheath with hemostatic valve, side port, atraumatic tip, braided shaft, uni- or bidirectional steerability, availability in small, medium or large curves, minimum inner diameter or 7F, minimum length of 65 cms. Should be FDA"/CE"/DCGI approved
112	38. 7 French quadripolar Radiofrequency ablation catheter with a 4 mm tip, unidirectional deflection, availability in small, medium and large curves. Should be compatible with Stockert and IBI RF generators and Suitable connecting cable should be provided for every 5 catheters.. Should be FDA"/CE"/DCGI approved
113	39. 7 French quadripolar Radiofrequency ablation catheter with a 4 mm tip, bidirectional deflection, availability in small, medium and large curves. Should be compatible with Stockert and IBI RF generators and suitable connecting cables should be provided . Should be FDA"/CE"/DCGI approved
114	40. 7 French quadripolar Radiofrequency ablation catheter with a 8 mm tip, unidirectional deflection, availability in medium and large curves. Should be compatible with Stockert and IBI RF generators and Suitable connecting cable should be provided for every 5 catheters.. Should be FDA"/CE"/DCGI approved
115	41. 7 French quadripolar Radiofrequency ablation catheter with irrigated tip, uni- or bi-directional deflection and availability in medium and large curves. Should be compatible with Stockert and IBI RF generators and Suitable connecting cable should be provided for every 5 catheters.. Should be FDA"/CE"/DCGI approved
116	42. Quadripolar, irrigated tip, Radiofrequency ablation catheter with a 3.5 mm tip and unidirectional deflection for use with the CARTO mapping system. Should include irrigation tubing set for interface between the irrigation pump and the ablation catheter and matching external reference patch for use with the CARTO 3 system. Should be FDA"/CE"/DCGI approved
117	43. CRT - Triple chamber pacing system comprising pacemaker, active atrial and ventricular leads and bipolar, over the wire coronary sinus lead. Should include long preshaped slittable sheaths for coronary sinus cannulation in multiple shapes, sub-selective inner sheaths, guidewire and occlusion balloon catheter for coronary venography. Coronary sinus lead should be available in multiple curves "/ sizes.. Should be FDA"/CE"/DCGI approved
118	44. Bipolar lead specially designed for placement in coronary sinus for LV pacing. Should be supplied with 9F short sheath with valve, long pre-shaped slittable sheaths in various shapes for CS cannulation and inner sub-selective sheath. Lead, long sheath, sub-selective sheath and short sheath should be quoted as one set.. Should be FDA"/CE"/DCGI approved
119	45. EMBOLIZATION COILS 035" all sizes. Should be FDA"/CE"/DCGI approved
120	46. EMBOLIZATION MICRO COILS 018 all sizes - Non Detachable and freely deliverable. Should be FDA"/CE"/DCGI approved
121	47. EMBOLIZATION MICRO COILS 018 all sizes -DETACHABLE 2D. Should be FDA"/CE"/DCGI approved
122	48. EMBOLISATION PARTICLES Poly Vinyl Alcohol all sizes. Should be FDA"/CE"/DCGI approved
123	49. Gelfoam (Powder or granule form) for Embolization. Should be FDA"/CE"/DCGI approved
124	50. MICROCATHETERS with Inbuilt hydrophilic wire for Peripheral Angiography and Particle /Coil delivery. Should be FDA"/CE"/DCGI approved
125	51. MICROCATHETERS - STEERABLE/ SHAPABLE with Inbuilt hydrophilic wire for Peripheral Angiography and Particle /Coil delivery. Should be FDA"/CE"/DCGI approved
126	52. Soft Guideliner for mother and child technique. Should be FDA" or CE" and DCGI approved
127	53. Rotablator Wire 009. Should be FDA"/CE"/DCGI approved
128	54. Rotablator Advancer. Should be FDA"/CE"/DCGI approved
129	55. Rotablator Burr. Should be FDA"/CE"/DCGI approved
130	56. ASD AMPLATZER TYPE SELF CENTRE DEVICES WITH ALL sizes from 8mm and above . Should be FDA approved
131	57. COOK SHEATHS (all sizes 6F-15F) with check flo valves) WITH ANGLED TIPS FOR ASD DEVICE DELIVERY. Should be FDA" or CE" and DCGI approved
132	58. PDA OCCUSION DEVICE --ALL CUSTOMISABLE SIZES WITH FROM 3MM TO 20MM WAIST SIZE . Should be FDA"/CE"/DCGI approved
133	59. PDA DELIVERY SYSTEMS AND INTRODUCER CABLE SYSTEMS . Should be FDA"/CE"/DCGI approved
134	60. Ventricular septal Closure Devices All sizes ( 4mm to18 mm). Should be FDA"/CE"/DCGI approved
135	61. Delivery cable and sheath set for Ventricular septal defect closure. Should be FDA" or CE" and DCGI approved