Purchase Of Consumable Items For Department Of Cr And Ei On Two Year Rate Contract Basis Purchase Of Consumable Items For Department Of Cr And Ei On Two Year Rate Contract Basis _1 , Purchase Of Various Consumable For Department Of Cr & Ei On Two Year Rate Contract Basis , Hydrophilic Diagnostic Guide Wire - ( Regular Length, Regular Stiffness ) , Hydrophilic Diagnostic Guide Wire - ( Exchange Length, Regular Stiffness ) , Hydrophilic Diagnostic Guide Wire – ( Regular Length, Extra-Stiff ) , Hydrophilic Diagnostic Guide Wire - ( Exchange Length, Extra-Stiff , Ptfe Coated Extrastiff Shaft Strength Wire- Backup Meier ( Regular Length ) , Ptfe Coated Extrastiff Shaft Strength Exchange Wire- Backup Meier ( Exchange Length ) , Nitinol 0.014 Inch Guidewire ( Exchange Length ) , Nitinol 0.018 Inch Guidewire ( Exchange Length ) , Heavy Duty Nitinol Alloy Extra Support Wire ( Regular Length ) , Heavy Duty Nitinol Alloy Extra Support Wire ( Exchange Length ) , Heavy Duty Nitinol Extra Support Wire ( Regular Length ) , Heavy Duty Nitinol Extra Support Wire ( Exchange Length ) , Steerable High Support .014 Inch Guidewire , Steerable High Support .014 Inch Guidewire ( Exchange ) , Cobra Catheter , Sos Omni Catheter , Tapered Straight Catheter , Picard Catheter , Renal Double Curve Catheter , Head Hunter Catheter , Simmons / Sidewinder Catheter , Preshaped Catheter For Uterine Artery Embolisation , Vertebral Catheter , Coeliac Axis Catheter , Shepherd’S Hook Catheter , Microcatheters ( Coiled Stainless Steel Construction ) , Microcatheters ( Braided Nitinol Construction ) , Straight Introducer Sheath ( Standard Length ) With Hydrophilic Introducer Guide Wire , Straight Long Introducer Sheath With Hydrophilic Introducer Guide Wire , Straight Reinforced Sheath With Hydrophilic Coating , Stearable Sheath , Radio-Opaque Marker Tape , Marker Pigtail Catheter – Fda Approved / Ce Marked , Guiding Catheter For Peripheral Vascular Use - 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 , Guiding Catheter For Peripheral Vascular Use – Should Be Braided With Low Friction Inner Layer - Should Have Hydrophilic Coating - Should Have Atraumatic Soft Tip - Should Be Available In Various Tip Shapes And Curves For Access To Different Parts Of The Peripheral Vasculature. - Should Have Od Of 6F-10F Available - Should Have The Largest Id For Each Od - Should Have Lengths Ranging From 55-125 Cm , Guiding Catheter For Peripheral Vascular Use – Should Be Braided With Low Friction Inner Layer - Should Have Hydrophilic Coating - Should Have Atraumatic Soft Tip - Should Be Available In Various Tip Shapes And Curves For Access To Different Parts Of The Peripheral Vasculature. - Should Have Od Of 5F Available With The Largest Od - Should Have A Minimum Length Of 55 Cm Or More , Long Sheath For Peripheral Vascular Access - Should Be Kink Resistant With A Reinforcement Mechanism - Should Be Low Friction With Inner Coating To Allow Catheter Manipulation - Should Have Distal Radio-Opaque Tip For Enhanced Visibility On Fluoroscopy - Should Have Smooth Transition From Dilator To Sheath - Should Have A Proximal Hemostasis Valve / Provision For Tuohy Borst Valve - Should Be Color Coded For Size Identification - Should Be Available In Various Sizes Of Inner Diameters And Various Lengths And Have The Largest Id , Long Sheath For Carotid Access - Should Be Kink Resistant With A Reinforcement Mechanism - Should Be Low Friction With Inner Coating To Allow Catheter Manipulation - Should Have Distal Radio-Opaque Tip For Enhanced Visibility On Fluoroscopy - Should Have Smooth Transition From Dilator To Sheath - Should Have A Proximal Hemostasis Valve / Provision For Tuohy Borst Valve - Should Be Color Coded For Size Identification - Should Be Available In 4F-8F Size With The Largest Id - Should Have A Minimum Length Of 90 Cm Or More , Long Sheath For Contra-Lateral Iliac / Femoral Access - Should Be Kink Resistant With A Reinforcement Mechanism - Should Be Low Friction With Inner Coating To Allow Catheter Manipulation - Should Have Distal Radio-Opaque Tip For Enhanced Visibility On Fluoroscopy - Should Have Smooth Transition From Dilator To Sheath - Should Have A Proximal Hemostasis Valve / Provision For Tuohy Borst Valve - Should Be Color Coded For Size Identification - Should Be Available In 4F-9F Size With The Largest Id - Should Have Lengths Ranging From 40- 110 Cm , Long Sheath For Liver Access - Should Be Kink Resistant - Should Have Distal Radio-Opaque Tip For Enhanced Visibility On Fluoroscopy - Should Have Smooth Transition From Dilator To Sheath - Should Have A Proximal Hemostasis Valve / Provision For Tuohy Borst Valve - Should Be Color Coded For Size Identification - Should Be Available In 9F And 10F Size With The Largest Id - Should Be At Least 38 Cm Long , High Pressure Angioplasty Balloon For Peripheral Vascular Use – Fda Approved / Ce Marked - Should Have Rated Burst Pressure > 14 Atmosphere - Should Have Hydrophilic Coating - Should Be Available In Various Outer Diameters And Balloon Lengths And Various Shaft Lengths , High Pressure Angioplasty Balloon For Peripheral Vascular Use – Fda Approved / Ce Marked - Should Have Rated Burst Pressure > 14 Atmosphere - Should Have Hydrophilic Coating - Should Be Available In 4-10 Mm ( In 1 Mm Increments ) And 12 Mm Diameters And 2-10 Cm Balloon Length - Should Have A Shaft Size Of 75-135 Cm , Peripheral Balloon Catheter – Fda Approved / Ce Marked - Should Be 0.035” Compatible - Should Be Over The Wire - Should Have A Burst Pressure Of At Least 10 Atmosphere ( At Least 6 Atmosphere For Larger Balloons ) - Should Have Hydrophilic Coating - Should Be Available In Various Sizes Of Od And Balloon Lengths -Should Be Available In Various Shaft Lengths , Peripheral Balloon Catheter With Large Diameter –Fda Approved / Ce Marked - Should Be 035” Compatible - Should Be Over The Wire - Should Have Hydrophilic Coating - Should Have Od Of 14 Mm And More - Various Lengths Of The Balloon Should Be Available - Should Be Mounted On Various Shaft Length , Peripheral Balloon Catheter – Fda Approved / Ce Marked - Should Be .014 / .018” Compatible - Should Be Over The Wire - Should Have Hydrophilic Coating - Should Be Available In Various Balloon Diameters - Should Be Available In Various Lengths Of The Balloon - Should Be Available In Various Shaft Lengths , Peripheral Balloon Catheter – Fda Approved / Ce Marked - Should Be .014 / .018” Compatible - Should Be Over The Wire - Should Be Controlled / Semi-Compliant Type - Should Have Hydrophilic Coating - Should Be Available In Ods Of 2-7 Mm - Should Be Available In All Balloon Lengths Of 2-4 Cm - Should Be Available In Shaft Lengths Of 80-150 Cm , Peripheral Balloon Catheter – Fda Approved / Ce Marked - Should Be .014 / .018”’Compatible - Should Be Rapid Exchange Type - Should Have Hydrophilic Coating - Should Be Available In Various Outer Balloon Diameters - Should Be Available In Various Balloon Lengths - Should Be Available In Various Shaft Lengths , Peripheral Cutting Balloon Catheter – Fda Approved / Ce Marked - Should Be Available In Balloon Od Of 3-6Mm - Should Have Upto 15 Mm Or Upto 20 Mm Working Length - Catheter Shaft Length Should Be Upto 140 Cm , Peripheral Compliant Balloon With Large Diameter – Fda Approved / Ce Marked - Should Be .035” Compatible - Should Have Od Ranging From 10-46 Mm - Should Have Shaft Length >90 Cm - Should Have Shaft Of Not More Than 8F Size - Should Pass Through A 12F Sheath , Peripheral Stent Balloon Mounted – Fda Approved / Ce Marked - Should Be .014 / .018” Compatible - Should Be Over The Wire - Should Be Made Of Stainless Steel Alloy - Should Have Balloon Od In The Range Of 4-7 Mm - Should Have Balloon / Stent Lengths In The Range Of 12-25 Mm - Should Have Shaft Lengths Of 80-150 Cm , Peripheral Stent Balloon Expandable – Fda Approved / Ce Marked - Should Be .014 / .018” Compatible - Should Be Over The Wire - Should Be Made Of Cobalt Chromium - Should Have Modular Design - Should Have Balloon Od Available In 4-7 Mm - Should Have Balloon / Stent Lengths Of 12-18 Mm - Should Have Shaft Lengths Of 80-150 Cm , Peripheral Stent Balloon Expandable – Fda Approved / Ce Marked - Should Be .014 / .018” Compatible - Should Be Rapid Exchange - Should Be Made Of Stainless Steel Alloy - Should Have Balloon Od In The Range Of 4-7 Mm - Should Have Balloon / Stent Lengths In The Range Of 12-25 Mm - Should Have Shaft Lengths Of 80-150 Cm , Peripheral Stent Balloon Expandable – Fda Approved / Ce Marked - Should Be 035” Compatible - Should Be Made Of Stainless Steel Or Cobalt Chromium - Should Be Quoted Either In Open Cell Or Closed Cell Design - Should Be Available In Various Balloon Ods - Should Have Various Balloon / Stent Lengths Available - Should Have A Shaft Length Of 75-135 Cm , Peripheral Stent Balloon Expandable – Fda Approved / Ce Marked - Should Be .035” Compatible - Should Be Made Of Stainless Steel - Should Have A Tandem Architecture Design - Should Have All Balloon Ods From 5-10 Mm In 1 Mm Increments - Should Have Available Various Balloon / Stent Lengths Of 20 To 55Mm - Should Have A Shaft Length Of 75 -135 Cm , Peripheral Stent Balloon Expandable – Fda Approved / Ce Marked - Should Be .035” Compatible - Should Be Made Of Stainless Steel - Should Be Laser Cut Slotted Tube With Closed Cell Design - Should Have Balloon Ods From 5-25 Mm, Bare Or Balloon Mounted - Should Have Available Various Balloon Stent / Lengths From 2-6 Cm - Should Have A Shaft Length Of Up To 135 Cm , Self-Expanding Peripheral Stent – Fda Approved / Ce Marked - Should Be .014 / 018” Compatible - Should Be Over The Wire - Should Be Made Of Nitinol - Should Have The Least Lesion Crossing Profile For All Stent Diameters - Should Be Available In Various Stent Diameters Of 6-10 Mm - Should Be Available In Various Stent Lengths From 20-40 Mm - Should Have A Shaft Length Of At Least 110 Cm , Self-Expanding Peripheral Stent – Fda Approved / Ce Marked - Should Be .014 / .018” Compatible - Should Be Over The Wire - Should Be Laser Cut Open Cell Nitinol Tube - Should Have A Low Lesion Crossing Profile - Should Be Available In All Stent Diameters Of 6-10 Mm - Should Be Available In Stent Lengths Of 2-6 Cm - Should Be On A Shaft Length Of 110-140 Cm , Self Expanding Peripheral Stent –Fda Approved / Ce Marked - Should Be .014 / .018” Compatible - Should Be Of Rapid Exchange Type - Should Be Made Of Nitinol - Should Be Available In Stent Lengths Of 3-4 Cm - Should Have A Minimum Shaft Length Of 110 Cm , Self-Expanding Peripheral Stent – Fda Approved / Ce Marked - Should Be .035” Compatible - Should Be Over The Wire - Should Be Made Of Nitinol - Should Be Available In Various Outer Diameters - Should Be Of Various Stent Lengths - Should Be On A Shaft Length Of 80-140 Cm , Self-Expanding Peripheral Stent – Fda Approved / Ce Marked - Should Be .035” Compatible - Should Be Over The Wire - Should Be Laser Cut From Single Nitinol Tube With No Welds - Should Be Available In Outer Diameters Of 5-14 Mm - Should Be Available In Stent Lengths Of 2-15 Cm - Should Be On A Shaft Length Of 80-140 Cm , Peripheral Self Expanding Stent Of Large Diameter- Fda Approved / Ce Marked - Should Be 035” Compatible - Should Be Made Of Nitinol Or Stainless Steel - Should Be Available In Outer Diameter Of 14-26 Mm - Should Be Available From 2-12 Cm In Stent Length - Should Be On A Minimum Shaft Length Of 110 Cm - Should Be Compatible With A 6-10 F Sheath , Peripheral Drug Eluting Stent - Should Have Any One Of The Following Drugs ( Sirulimus, Evorolimus, Zotarolimus, Paclitaxel ) Impregnated On The Stent - Should Be Balloon Mounted Or Self –Expanding Type - Should Be Available In Various Outer Diameters - Should Be Available In Various Lengths , Peripheral Bio-Degradable Or Absorbable Metal Stent - Should Be Balloon Mounted Or Self-Expanding Type - Should Be Available In Various Outer Diameters - Should Be Available In Various Lengths , Self Expanding Peripheral Covered Stents – Fda Approved / Ce Marked - Should Be .035” Compatible - Should Be Over The Wire - Should Be Available In Various Outer Diameters - Should Be Available In Various Stent Lengths - Should Be On A Shaft Length Of 80-140 Cm. , Balloon Mounted Peripheral Covered Stents - In Various Diameter And Length , Self Expanding Peripheral Covered Stents – Fda Approved / Ce Marked - Should Be .035” Compatible - Should Be Over The Wire - Should Be Made Of Nitinol With Ptfe Coating On The Inner Lumen - Should Be Available In Outer Diameters Of 5-13 Mm - Should Be Avaiable In Stent Lengths Of 2-15 Cm - Should Be On A Shaft Length Of 75-140 Cm , Covered Stent For Transjugular Intrahepatic Porto-Systemic Shunt –Fda Approved / Ce Marked - Should Be .035 / 038” Compatible - Should Be Made Of Nitinol With Fabric Coating - Should Be With Or Without A Distal Uncovered Portion - Should Be Available In Various Outer Diameters And Stent Lengths - Should Be Compatible With The Quoted Tips Set , Embolization Coils -Pushable - Should Be .014 / 018” / .035 / 038” Compatible - Should Be Made Of Platinum With Synthetic Fibres - Should Be Non Tapering / Straight - Should Be Mr Compatible - Should Be Available In Multiple Diameter And Length -Should Be Pushable , Embolization Coils -Detachable - Should Be .014 / 018” / .035 / 038” Compatible - Should Be Made Of Platinum With Synthetic Fibres - Should Be Non Tapering / Straight - Should Be Mr Compatible - Should Be Available In Multiple Diameter And Length -Should Be Detachable , Embolization Coils -Packing - Should Be .014 / 018” / .035 / 038” Compatible - Should Be Made Of Platinum With Synthetic Fibres - Should Be Non Tapering / Straight - Should Be Mr Compatible - Should Be Available In Multiple Diameter And Length -For Packing Of Aneurysm , Embolization Coils-Bare Metal - Should Be .014 / 018” / .035 / 038” Compatible - Should Be Made Of Bare Metal - Should Be Mr Compatible - Should Be Tapering From A Larger To A Smaller End - Should Be Available In Multiple Diameter And Length -Should Be Pushable / Detachable , Embolization Coils - Should Be .035 / 038 / 052 Compatible - Should Be Non Tapering / Straight - Should Be Made Of Stainless Steel With Synthetic Fibres - Should Be Available In The Following Sizes: Diameter 3-15 Mm And Length 2-15 Cm , Coil Pusher Wire For 0.014 / 0.018” Coils, Compatible With The Quoted Microcatheters , Polyvinyl Alcohol Particles For Peripheral Vascular Embolization - Should Be Of Non-Uniform Size - Should Undergo Rapid Clumping In The Vessels - Should Cause Non-Uniform Vessel Occlusion - Should Be Available In A Broad Range Of Sizes ( 90 Microns- 1400 Micron ) , Microspheres For Peripheral Vascular Embolization - Should Be Hydrophilic - Should Be Micro-Porous And Uniform Sized Spheres - Should Be Non-Aggregating - Should Be Deformable For Ease Of Passage Through Smaller Vessels - The Size Of Spheres Should Range From40-1200 Micrometers , Gelfoam Sheet For Vascular Embolization , Non-Adhesive Liquid Polymer For Controlled Embolization - Should Be Ethylene Vinyl Copolymer In Dimethylsulfoxide Solution - Should Be Supplied In Various Concentrations For Use Depending On Lesion Morphology , Adhesive Liquid Polymer For Vascular Embolization - Should Be N-Butyl Cyanoacrylate , Tantalum Powder -Should Be Useful For Improved Visualization During N-Butyl Cyanoacrylate Embolization - Should Be Supplied As Finely Ground Powder , Lipiodol - The Material Should Be Iodised Oil, Containing Ethyl Esters Of Iodized Fatty Acids Of Poppy Seed Oil - The Iodine Content Should Be A Minimum Of 480 Mg / Ml - Should Useful As Opacifying Agent For N-Butyl Cyanoacrylate On Fluoroscopy And An Organic Diluents For This Agent Should Be Supplied In 10 Ml Ampoules , Sclerosant For Intravenous Embolization ( Sodium Tetradecyl Sulfate ) - The Compound Should Be Sodium Tetradecyl Sulfate - Should Be Available In Various Concentrations For Use Depending On Lesion Type , Sclerosant For Intravenous Embolization ( Polidocanol ) - The Compound Should Bepolidocanol - Should Be Available In Various Concentrations For Use Depending On Lesion Type , Detachable Balloon For Embolization - Detachable Balloons With Radioopaque Marker With And Without Self-Sealing Valve - 0.1 Cc – 3 Cc Or More In Capacity - Please Specify The Make And Capacity Of The Balloons ( Latex / Silicon ) . - The Catheter Shaft Should Be Of At Least 120 Cm In Length , Ivc Filter - For Optimal Filtration Of Ivc Diameter Of Upto 40 Mm - Made Of Nitinol - Catheter Carrier System Inner Diameter Should Be Of Maximum 12F - It Should Be Possible To Insert From Either Jugular Or Femoral Access - Should Be For Permanent Use , Ivc Filter - For Optimal Filtration Of Ivc Diameter Of Upto 40 Mm - Made Of Stainless Steel - Catheter Carrier System Inner Diameter Should Be Of Maximum 12F - It Should Be Possible To Insert From Either Jugular Or Femoral Access - Should Be For Permanent Use , Ivc Filter - For Optimal Filtration Of Ivc Diameter Of Upto 28 Mm - Made Of Nitinol And Filter Length To Be Upto 38 Mm - Catheter Carrier System Inner Diameter Should Be Of Maximum 7F Size - It Should Be For Optional Use - It Should Be Possible To Place The Filter From Femoral / Jugular / Antecubital Access , Ivc Filter - For Optimal Filtration Of Ivc Diameter Of Upto 28 Mm - Made Of Stainless Steel With Carbon Or Heparin Coating And Filter Length To Be Upto 38 Mm - Catheter Carrier System Inner Diameter Should Be Of Maximum 7 F Size - It Should Be For Optional Use - It Should Be Possible To Place The Filter From Femoral / Jugular / Antecubital Access , Ivc Filter - For Optimal Filtration Of Ivc Diameter Of Upto 28 Mm - Made Of Nitino Material And Filter Length Not More Than 55 Mm - Catheter Carrier System Inner Diameter Should Be Of Maximum 10 F Size - Should Be Able To Be Placed Either Through Jugular Or Femoral Approach - Should Be For Optional Use , Ivc Filter - For Optimal Filtration Of Ivc Diameter Of Upto 30 Mm - Made Of Conichrome Material And Filter Length Not More Than 50 Mm - Should Be Able To Be Placed Either Through Jugular Or Femoral Approach - Should Be For Optional Use , Percutaneous Mechanical Thrombectomy Catheter - Should Allow Treatment Of Fresh And Older Thrombotic Occlusions Of Peripheral Arteries - Should Combines Mechanical Fragmentation And Aspiration Alongwith Transport Of Debris Outside The Vascular System - Should Be Available In Both Antegrade Or Cross-Over Configurations , Infusion Catheter - Should Have Multiple Side Ports - Should Provide An Infusion Length Of 5-15 Cm - Should Have A Catheter Tip Occluder - Should Have Attachment For Tuohy-Borst Side Arm Adapter - Should Be Compatible With 035 / 038” Wire - Should Have A Shaft Length Of 100 Cm , Embolic Protection Device - Should Be On A .014” Wire - Should Be Made Of Nitinol Material - Should Not Occlude Flow While In Placement - Should Be Rapid Exchange Type - Should Allow Use Of A Separate .014 / 018” Wire For Initial Crossing Of The Lesion - Should Be Compatible With A 6F Guiding Catheter ( 0.066” Id ) - Should Allow Longitudinal Wire Movement With Filter Remaining In Place - Should Be Available In Various Sizes , Embolic Protection Device - Should Be On A .014” Wire - Should Be Made Of Nitinol With Covering Membrane - Should Be Of Umbrella Shape With Self-Centering Capability - Should Not Occlude Flow While In Placement - Should Be Rapid Exchange Type - Should Be Compatible With A Maximum Of 8F Guiding Catheter - Should Allow Optimal Filtration In Vessels 3.5-7.5 Mm Sizes - The Filter Wire Should Be At Least 180 Cm Long , Embolic Protection Device - Should Be On A .014” Wire - 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 6F Guiding Cathether ( 0.066” Id ) - Should Allow Optimal Filtration In Vessels 3.5-5.5 Mm Size , Peripheral Vascular Catheter For Excision Of Atheroma- Should Have High Rotation Speed Of The Cutting Mechanism Without Causing Any Trauma To The Vessel -Vendor Should Specify Detail Of Catheter Quoted , Catheter For Crossing Chronic Total Occlusions In Peripheral Arteries - Vendor Should Specify Detail Of Catheter Quoted , Micro Puncture Set - Should Be Transitionless - Outer Catheter Varying From 3-5 F, 10-22Cm Long - 018 Nitinol Wire, 40 Cm Long - With Hemostasis Valve - With Side Arm - Needle Should Be 21 G Or Less, 4-7 Cm Long With Preferably Echogenic Needle , Percutaneous Thin Wall Needles For Single Puncture - 21 G - 018 Wire Compatible - Length 2-15 Cm Long , Pedal Sheath With Nitinol Wire - 018 Wire Compatible - 4-6 F Size - Sheath Length 4 To 13 Cm Long - 21 G Needle, Needle Length 4 Cm To 7 Cm - Nitinol Guidewire , Pedal Sheath With Stainless Steel Wire - 018 Wire Compatible - 4, 5, 6 F Size - Sheath Length 4 To 13 Cm Long - 21 G Needle, Needle Length 4 Cm To 7 Cm - Stainless Steel Guidewire , 0.014 Wire Compatible Local Infusion Catheter With Balloon - Should Have Micro Porous Ptfe Balloon For Drug Infusion - Rapid Exchange Platform - Should Be Able To Infuse Drug Controllably - Balloon Diameter Should Be 1, 1.5, 2, 2.5, 3, 4, 5 Mm With 10Mm, 20, 50, Mm Lengths - Catheter Should Be 90 To 150 Cm Long , 035 Wire Compatible Local Infusion Catheter With Balloon - Should Have Micro Porous Ptfe Balloon For Drug Infusion - Over The Wire Platform - Should Be Able To Infuse Drug Controllably - Balloon Diameter Should Be 4-8 Mm With 10 To 50 Mm Lengths - Catheter Should Be 80 To 150 Cm Long , 018 Non Compliant Balloon ( Rapid Exchange Platform ) - 2-8 Mm Diameter - 20-300Mm Long - Should Ideally Pass Through 4 F Sheath - Shaft Length 20 -230 Cm Long - Should Have Double Lumen Shaft Construction - Should Preferably Have Lubricious Coating On Balloon And Delivery Stem , Closed Cell Cobalt Chromium Balloon Expandable Stent On Over The Wire Platform - 014 Wire Compatible - Diameters 2, 2.5, 3, 3.5, 4, 4.5, 5 Mm - Length 10 -100Mm - Shaft Length 90-170 Cm Long - Should Pass Through 5 F Sheath , Nitinol Self Expandable 018 Wire Compatible Rapid Exchange Stent - 018 Wire Compatible - Diameters 2, 2.5, 3, 3.5, 4, 4.5, 5 Mm - Length 10 -200Mm - Shaft Length 90-180 Cm Long - Should Pass Through 4 F Sheath - Should Have Low Strut Profile - Should Have Stent Markers At Each End - Preferably Should Have Resistance Free Coating , Endovascular Stent Graft Device For Treatment Of Thoracic Aortic Aneurysms And Dissections – Fda / Ceapproved -Device Should Be With Proximal Barbs, With Or Without Distal Bare Spring Configuration, And Should Be Either Tapered Or Non-Tapered, Should Be Either Free Flow Or Covered Configuration, -The Aortic Device Should Be Available In The Following Sizes In Non-Tapered: Diameter 20-46Mm; Length 96-223Cm. -The Aortic Device Should Be Available In The Following Sizes In Tapered: Diameter 25-46Mm; Length 173-200Cm. -The Device Should Be Able To Be Advanced On Upto 24F Shaft Size. , Endovascular Stent Graft Device For Treatment Of Thoracic Aortic Aneurysms And Dissections- Fdaapproved / Ceapproved -Device Should Be With Proximal Barbs, With Or Without Distal Bare Spring Configuration, And Should Be Either Tapered Or Non-Tapered, Should Be Either Free Flow Or Covered Configuration With / Without Tip Capture -The Aortic Device Should Be Available In The Following Sizes In Non-Tapered: Diameter Min- ( 20-24 Mm ) And Max . 46Mm; Length 100-200 Cm+ / - 20 Cm. -The Aortic Device Should Be Available Inthe Following Sizes In Tapered: Diameter 26-46Mm; Length 150Cm. -The Device Should Be Able To Be Advanced On Upto 24F Shaft Size. , Endovascular Stent Graft Device For Treatment Of Thoracic Aortic Aneurysms And Dissections-Fda / Ce Approved -Device Should Be With Proximal Barbs, With Or Without Distal Bare Spring Configuration, And Should Be Either Tapered Or Non-Tapered, Should Be Either Free Flow Or Covered Configuration With / Without Tip Capture -The Aortic Device Should Be Available Various Sizes Intapered And Non-Tapered Diameter And Lengths , Endoanchor Device For Treatment Of Thoracic Aortic Aneurysms And Dissections, Stent Graft Migration & Type I Endoleaks -Device Should Be Available With Working Length Of Either 90 Or 114Cm -The Device Should Be Able To Be Advanced On Upto 24F Shaft Size. , Endovascular Stent Graft Device For Treatment Of Thoracic Aortic Aneurysms And Dissections- Fda / Ce Approved -Device Should Be With Proximal Barbs, With Or Without Distal Bare Spring Configuration, And Should Be Either Tapered Or Non-Tapered. -The Aortic Device Should Be Available In Any One Or More Of The Following Sizes In Non-Tapered: Diameter 24-46Mm; Length 105-233Cm. -The Aortic Device Should Be Available In Any One Or More Of The Following Sizes In Tapered: Diameter 32-46Mm; Length 178-233Cm. -The Distal Extensions Of The Should Be Available In 28-46Mm Diameters; Length: 108-233Cm. -The Device Should Be Able To Be Advanced On Upto 24F Shaft Size. , Endovascular Stent Graft Device For Treatment Of Thoracic Aortic Dissections- Fda / Ce Approved -Device Should Be With Proximal Barbs, With Or Without Distal Bare Spring Configuration, And Should Be Either Tapered Or Non-Tapered. -The Aortic Device Should Be Available In Any One Or More Of The Following Sizes In Non-Tapered: Diameter 22-42Mm; Length 79-218Cm. -The Aortic Device Should Be Available In Any One Or More Of The Following Sizes In Tapered: Diameter 32-42Mm; Length 162-210Cm, Tapered Length 4-8Mm. -The Device Should Be Able To Be Advanced On Upto 24F 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- Fda / Ce Approved -Device Should Be With Proximal Barbs, With Or Without Distal Bare Spring Configuration, And Should Be Either Tapered Or Non-Tapered, Should Have Supporting Strut On The Greater Curvature -The Aortic Device Should Be Available In Wide Range Of Diameter And Lengths -The Device Should Be Able To Be Advanced On Upto 24F Shaft Size. , Endovascular Stent Graft Device For Treatment Of Abdominal Aortic Aneurysms - Fda / Ce Approved -Device Should Be With Or Without Proximal Barbs, With Or Without Distal Bare Spring Configuration, And Should Be Either Tapered Or Non-Tapered, Should Be Either Bifurcated Or Aorto-Uniliac Configuration. -Devices With Or Without Transrenal Or Suprarenal Fixation Should Be Quoted. -The Main Body Aortic Device Should Be Available In Any One Or More Of The Following Sizes: Diameter 23-36 Mm; Length 124- 166Cm. -The Limb Extensions Of The Main Device For Abdominal Aortic Applications Should Be Available In 16Mm Diameter, With Or Without Flared Ends. -The Aortic Extensions Of The Main Device For Abdominal Aortic Applications Should Be Available In Diameter 23-36Mm Diameters -The Iliac Extensions Of The Should Be Available In 10-28Mm Diameters. , Endovascular Stent Graft Device For Treatment Of Abdominal Aortic Aneurysms -Fda / Ceapproved -Device Should Be With Or Without Proximal Barbs, With Or Without Distal Bare Spring Configuration, And Should Be Either Tapered Or Non-Tapered, Should Be Either Bifurcated Or Aorto-Uniliac Configuration. -Devices With Or Without Transrenal Or Suprarenal Fixation Should Be Quoted. -The Main Body Aortic Device Should Be Available In Wide Range Of Diameter And Length -The Limb Extensions Of The Main Device For Abdominal Aortic Applications Should Be Available In Suitable Diameter, With Or Without Flared Ends. -The Aortic Extensions Of The Main Device For Abdominal Aortic Applications Should Be Available In Wide Diameter Range -The Iliac Extensions Of The Should Be Available In Wide Diameter Range , Endoanchor Device For Treatment Of Abdominal Aortic Aneurysms, Stent Graft Migration & Type I Endoleaks -Device Should Be Available With Working Length Of Either 62 Or 86Cm -The Device Should Be Able To Be Advanced On Upto 24F Shaft Size. , Endovascular Stent Graft Device For Secondary Endovascular Intervention In Patients Having Received Prior Endovascular Repair Of Infrarenal Abdominal Aortic Or Aorto-Iliac Aneurysms Fda / Ceapproved -Device Should Be With Or Without Proximal Barbs, With Or Without Distal Bare Spring Configuration, And Should Be Either Tapered Or Non-Tapered, Should Be Either Bifurcated Or Aorto-Uniliac Configuration. -Devices With Or Without Transrenal Or Suprarenal Fixation Should Be Quoted. -The Main Body Aortic Device Should Be Available In Any One Or More Of The Following Sizes: Diameter 22-36 Mm; Length 43-100Cm. , Endovascular Stent Graft Device For Treatment Of Abdominal Aortic Aneurysms – Fda / Ce Approved -Device Should Be With Or Without Proximal Barbs, With Or Without Distal Bare Spring Configuration, And Should Be Either Tapered Or Non-Tapered, Should Be Either Bifurcated Or Aorto-Uniliac Configuration And Must Have Fenestration. -Devices With Or Without Transrenal Or Suprarenal Fixation Should Be Quoted. -The Proximal Body Aortic Device Should Be Available In Various Diameters And Lengths -The Distal Body Aortic Device Should Be Available In Various Diameters And Lengths , Endovascular Stent Graft Device For Treatment Of Abdominal Aortic Aneurysms – Fda / Ce Approved -Device Should Be With Or Without Proximal Barbs, With Or Without Distal Bare Spring Configuration, And Should Be Either Tapered Or Non-Tapered, Should Be Either Bifurcated Or Aorto-Uniliac Configuration. -Devices With Or Without Transrenal Or Suprarenal Fixation Should Be Quoted. -The Bifurcated Aortic Device Should Be Available In Suitable Diameter And Lengths -The Aorta Uniiliac Device Should Be Available In Suitable Diameters And Lengths -The Limb Extensions Of The Main Device For Abdominal Aortic Applications Should Be Available In Various Sutable Diameters And Lengths With Or Without Flared Ends. , Endovascular Stent Graft Device For Treatment Of Abdominal Aortic Aneurysms With Larger Infra Renal Neck Angulations- Fda / Ceapproved • Device Should Be With Or Without Proximal Barbs, With Or Without Distal Bare Spring Configuration, And Should Be Either Tapered Or Non-Tapered, Should Be Either Bifurcated Or Aorto-Uniliac Configuration. • Devices With Or Without Transrenal Or Suprarenal Fixation Should Be Quoted. • The Bifurcated Aortic Device Should Be Available In Suitable Diameter And Lengths • The Limb Extensions Of The Main Device For Abdominal Aortic Applications Should Be Available In Suitable Diameter And Lengths • The Iliac Limb Extensions Should Be Available In Suitable Diameter And Legths, With And Without Distal Flared Ends. , Endovascular Stent Graft Device For Treatment Of Abdominal Aortic Aneurysms With Larger Infra Renal Neck Angulations -Fda / Ce Approved • Device Should Be With Or Without Proximal Barbs, With Or Without Distal Bare Spring Configuration, Should Be Either Bifurcated Or Aorto-Uniliac Configuration. • Devices With Or Without Transrenal Or Suprarenal Fixation Should Be Quoted. • Devices Should Having Branch Graft For Visceral Vessels Fixation Should Be Quoted. • The Aortic Device Should Be Available In Suitable Diameter And Lengths • The Limb Extensions Of The Main Device For Abdominal Aortic Applications Should Be Available In Various Diameter And Length With Or Without Flared Ends. , Covered Stent-Graft ( Extender Or Iliac Or Contralateral Limb ) In Diameters Ranging From12-22 Mm And Lengths Ranging From 30-110 Mm For Over-The-Wire Delivery. , Endovascular Stent Graft With Iliac Branch Devices For Treatment Of Aorto Iliac Aneurysm Fda / Ce Approved -In Straight / Curved Iliac Branch Device Configuration -Various Suitable Diameter And Lengths Of Aortic And Iliac Devices , Vascular Closure Device Fda / Ceapproved - Plug / Suture / Nitinol Based - Should Be Available Invarious Sizes Of Arterial Access
