Employees State Insurance Corporation invites bids for X-Ray Detectable Gauze Swab/Laparotomy Sponge (V2) (Q2). Quantity: 5000. Submission Deadline: 27-10-2025 12: 00: 00. Submit your proposal before the deadline.
GEM
Government Tender Published for X-Ray Detectable Gauze Swab/Laparotomy Sponge (V2)
Posted
16 Oct 2025, 11:19 am
Deadline
27 Oct 2025, 12:00 pm
Progress
Issue16 Oct 2025, 11:19 am
AwardPending
Quantity
5000
Bid Type
Two Packet Bid
Categories
1
Technical Specifications
1 Item
Item #1 Details
View Catalog| Category | Specification | Requirement |
|---|---|---|
| GENERAL | Product Description | X-Ray Detectable Gauze Swab / Laparotomy Sponge |
| GENERAL | Purpose | Intended for Medical Use |
| GENERAL | Sterility | Sterile, Non-Sterile |
| STANDARD | Conformity to Standard | IS 10829 (Latest) |
| PRODUCT INFORMATION | Consist of folded absorbent gauze attached with a non-toxic and distinctively coloured X-ray detectable member | Yes |
| PRODUCT INFORMATION | Manufacture, Workmanship and Finish shall be as per IS 10829 (Latest) | Yes |
| PRODUCT INFORMATION | Absorbent gauze shall conform to the requirements given in Table 1 of IS 10829 (Latest) | Yes |
| PRODUCT INFORMATION | Size (Width x Length) | 30 cm x 30 cm |
| PRODUCT INFORMATION | Number of Plies | 12 |
| PRODUCT INFORMATION | Attached with braided cotton tape at one end | Yes |
| PRODUCT INFORMATION | Width of braided cotton tape | 10 mm |
| PRODUCT INFORMATION | Tolerance on length and width shall be as per IS 10829 Latest | Yes |
| PACKING & MARKING | Packaging & Marking shall be as per IS 10829 (Latest) | Yes |
| CERTIFICATIONS | Compliance to Medical Device Rules (MDR) 2017 as amended till date | Yes |
| CERTIFICATIONS | Availability of valid medical device license number for the product issued from the competent authority defined under Drugs and Cosmetic Act 1940 and Rules made there under as amended till date | Yes |
| CERTIFICATIONS | ISO:13485 (Latest) certification | Yes |
| CERTIFICATIONS | Availability of Test Report for each supplied batch/product as per Medical Device Rule (MDR) 2017 as amended till date | Yes |
| CERTIFICATIONS | Submission of all necessary certifications, licenses and test reports to the buyer at the time of bid submission or along with supplies as per buyer requirement | Yes |
| SHELF LIFE | Shelf life from the date of manufacture | 36, 60 Or higher |
| SHELF LIFE | Minimum shelf life of the product at the time of delivery to the consignee | 3/4 th of Total Shelf Life |
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Required Documents
1
OEM Authorization Certificate *In case any bidder is seeking exemption from Experience / Turnover Criteria
2
the supporting documents to prove his eligibility for exemption must be uploaded for evaluation by the buyer
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Documents 3
GeM-Bidding-8480637.pdf
Main Document
CATALOG-Specification-1
CATALOG Specification
GEM General Terms and Conditions Document
GEM_GENERAL_TERMS_AND_CONDITIONS
GeM-Bidding-8480637.pdf
Main Document
CATALOG-Specification-1
CATALOG Specification
GEM General Terms and Conditions Document
GEM_GENERAL_TERMS_AND_CONDITIONS