BRR : 11579736
Click Here To View Tendering Authority. Aoc City/State :  , Tamil Nadu
Tender Brief : Supply Of des-abbreviated dapt long -coronary drug eluting stents (stent diameter should be from 2.5mm to 4mm. the length of the stent should be from 12mm to 48 mm, the strut thickness should be 91 micron or less) , srphc82281275-des-abbreviated dapt long -coronary drug eluting stents w ith (1) platinum chromium alloy (2) coating of bioabsorbable polymer carrier for active drug everolimus 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 t o 48 mm. (4) the strut thickness should be 91 micron... Read More
Tender Value
Ref. Document
Contract Value
₹ 24,68,718
Submission Date
15-06-2026
Contract Date
13-07-2026
Completion Date
Ref. Document
Participated Bidder List
1 No of Bidder(s)
Sr No. Bidder Name Bid Analytics Technical Bid Financial Bid AOC Bid Value Rank
1 cnet-technologies Bid Analytics 24,68,718 L1
Work Detail
supply of des-abbreviated dapt long -coronary drug eluting stents (stent diameter should be from 2.5mm to 4mm. the length of the stent should be from 12mm to 48 mm, the strut thickness should be 91 micron or less) , srphc82281275-des-abbreviated dapt long -coronary drug eluting stents w ith (1) platinum chromium alloy (2) coating of bioabsorbable polymer carrier for active drug everolimus 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 t o 48 mm. (4) the strut thickness should be 91 micron or less. (5) stent delivery system s hould be monorail (single operator exchange or rapid exchange). (6) stent should be c ompatible 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 tende r bid. (9) the long term efficacy and safety of the stent, the rates of in-stent restenosi s (isr) and in-situ thrombosis (ist) should be documented / published in peer reviewed sc ientific journals. (10) safety of abbreviated (three month) dual antiplatelet therapy fo r high bleeding risk patients should be documented in peer reviewed journals. (11) the manufacturer/supplier should submit proof of supply of the stent to a major governme nt institute. bis standards for the drug eluting stent are not available. (reference:bis catalogue ). [quantity tolerance (+/-): 5 %age , item category : normal , total po value variation permitt ed: max 8 lacs ] ]
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Awarded Bidder(s)
1
cnet-technologies
Rank : L1 (Lowest)
Bid Amount : ₹ 1,00,00,000
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