SRPHC153053-CORONARY DRUG ELUTING STENTS (1) WITH SINGLE WIRE DESIGN WITH COBALT ALLOY SHELL AND PLATINUM IRIDIUM CORE (2) STENT WITH COATING OF BIOLINX POLYMER CARRIER FOR ACTIVE DRUG ZOTAROLIMUS SHOWN TO BE EFFECTIVE IN PREVENTING NEO-INTIMAL HYPERPLASIA (3) STENT DIAMETER SHOULD BE FROM 2 MM TO 5MM AND LENGTH OF THE STENT FROM 8 MM TO 38 MM. (4) THE STRUT SHOULD BE ROUND WITH THICKNESS RANGING FROM 81 TO 91 MICRONS (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. (9) FIVE YEARS EFFICACY AND SAFETY OF THE STENT IN TERMS OF TARGET VESSEL REVASCULARISATION (TVR) AND IN-SITU THROMBOSIS (IST) SHOULD BE DOCUMENTED / PUBLISHED IN PEER REVIEWED SCIENTIFIC JOURNALS.(10) THE DOCUMENTS PERTAINING TO THE EFFICACY AND SAFETY OF THE STENT SHOULD BE ENCLOSED FOR THE BRAND THAT IS OFFERED IN THE TENDER BID (11) THE MANUFACTURER/SUPPLIER SHOULD SUBMIT PROOF OF SUPPLY OF THE STENT TO A MAJOR GOVERNMENT INSTITUTE. UNIT:NO[Quantity Tolerance (+/-): 5 %age , Item Category : Normal , Total PO value variation Permitted: Max 8 lacs ] ]
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