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Tender For Coronary Drug Eluting Stents, perambur-Tamil Nadu

Southern Railway-SR has published Tender For Coronary Drug Eluting Stents. Submission Date for this Tender is 07-08-2023. Stents Tenders in perambur Tamil Nadu. Bidders can get complete Tender details and download the document.




Tender Notice

38964418
Tender For Coronary Drug Eluting Stents
Open Tender
Indian
Tamil Nadu
perambur
07-08-2023

Tender Details

Supply Of ( Sr Ph Code 153041 ) Coronary Drug Eluting Stents With ( 1 ) Stent On Cobalt Chromium Alloy Or Platinum Chromium Alloy. ( 2 ) Stent With Coating Of Polymer Carrier For Active Drug ( Sirolimus, Everolimus Or Zotarolimus Shown To Be Effective In Preventing Neo-Intimal Hyperplasia ) ( 3 ) Stent Diameter Should Be From 2.5Mm To 4Mm . The Length Of The Stent Should Be From 12Mm To 38 Mm . ( 4 ) The Strut Thickness Should Be 91 Micron Or Less. ( 5 ) Stent Delivery System Should Be Monorail ( Single Operator Exchange Or Rapid Exchange ) . ( 6 ) Stent Should Be Compatible With 5Fr Guiding Catheter ( 7 ) Stent Design Should Be Open Cell Type. ( 8 ) Stent Should Be Approved By Dcgi. The Copy Of Dcgi Approval Should Be Enclosed In The Tender Bid / Offer. ( 9 ) The Long Term Efficacy And Safety Of The Stent, The Rates Of In-Stent Restenosis ( Isr ) And In-Situ Thrombosis ( Ist ) Should Be Documented / Published In Peer Reviewed Scientific Journals. ( 10 ) The Manufacturer / Supplier Should Submit Proof Of Supply Of The Stent To A Major Government Institute.Bis Standards For The Drug Eluting Stent Are Not Available ( Reference : Bis Catalogue ) Unit: No

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BOQ Items

Sl. No. Item Description
1Coronary Drug Eluting Stents
2( SR PH CODE 153041 ) CORONARY DRUG ELUTING STENTS WITH (1) STENT ON COBALT CHROMIUM ALLOY OR PLATINUM CHROMIUM ALLOY. (2) STENT WITH COATING OF POLYMER CARRIER FOR ACTIVE DRUG ( SIROLIMUS, EVEROLIMUS OR ZOTAROLIMUS SHOWN TO BE EFFECTIVE IN PREVENTING NEO-INTIMAL HYPERPLASIA) (3) STENT DIAMETER SHOULD BE FROM 2.5MM TO 4MM . THE LENGTH OF THE STENT SHOULD BE FROM 12MM TO 38 MM . (4) THE STRUT THICKNESS SHOULD BE 91 MICRON OR LESS. (5) STENT DELIVERY SYSTEM SHOULD BE MONORAIL (SINGLE OPERATOR EXCHANGE OR RAPID EXCHANGE). (6) STENT SHOULD BE COMPATIBLE WITH 5FR GUIDING CATHETER (7) STENT DESIGN SHOULD BE OPEN CELL TYPE. (8) STENT SHOULD BE APPROVED BY DCGI. THE COPY OF DCGI APPROVAL SHOULD BE ENCLOSED IN THE TENDER BID / OFFER. (9) THE LONG TERM EFFICACY AND SAFETY OF THE STENT, THE RATES OF IN-STENT RESTENOSIS (ISR) AND IN-SITU THROMBOSIS (IST) SHOULD BE DOCUMENTED / PUBLISHED IN PEER REVIEWED SCIENTIFIC JOURNALS. (10)THE MANUFACTURER/SUPPLIER SHOULD SUBMIT PROOF OF SUPPLY OF THE STENT TO A MAJOR GOVERNMENT INSTITUTE.BIS STANDARDS FOR THE DRUG ELUTING STENT ARE NOT AVAILABLE (REFERENCE : BIS CATALOGUE ) UNIT: NO
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