| 1 |
Fee/PreQual/Technical |
EMD Scan Copy |
.pdf |
|
|
Documentary evidence for the constitution of the company |
.pdf |
|
|
The instruments such as power of attorney |
.pdf |
|
|
Authorization letter nominating a responsible person |
.pdf |
|
|
Annual turnover statement for any 3 financial years |
.pdf |
|
|
GST Registration certificate (stating Tin Number) |
.pdf |
|
|
Checklist (Annexure XIV) |
.pdf |
|
|
Attested photocopy of manufacturing license for the product/Group of products |
.pdf |
|
|
Market Standing cum performance Certificate |
.pdf |
|
|
Duly attested photocopy of Import License, if importer |
.pdf |
|
|
Declaration (as per format in Annexure-VII |
.pdf |
|
|
Original Manufacturers ISI/ISO/CE/USFDA/FDA/WHO-GMP certificates |
.pdf |
|
|
List of items quoted without rates. (As per format in Annexure- IX). |
.pdf |
|
|
Mandate form. (As per format in Annexure-X). |
.pdf |
|
|
Production capacity certificate |
.pdf |
|
|
COMPLIANCE TO TECHNICAL SPECIFICATION |
.pdf |
|
|
Details of Manufacturing Unit from Which Product Will Be Supplied VI. |
.pdf |
|
|
Minimum 01 year safety and efficacy data of stent published in index national / international |
.pdf |
|
|
Clarification documents |
.pdf |
|
|
Declaration form on minimum Rs. 100 Non Judicial stamp paper Annexure XVI |
.pdf |
|
|
Bidder/Firm must replace all types of Stent and balloons free of cost before 06 months of expiry. |
.pdf |
|
|
CE / USFDA is mandatory for all Items |
.pdf |
|
|
In case a coronary stent/ peripheral stent (or both) is opened but not successfully crossed |
.pdf |
|
|
Stent which is not crossed should be replaced by firm without any cost. |
.pdf |
|
|
Bidder must submit Merged Single PDF of all the above technical documents |
.pdf |
|
|
Bidder must submit Check list II (Annexure XVIII), in excel format |
.xls |
|
|
Other Documents if any |
.pdf |
| 2 |
Finance |
Price Sheet |
.xls |