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Procurement Opportunity: Knee Braces and Splints (V2) in KOLLAM, KERALA

Bid Publish Date

19-Jun-2026, 3:34 pm

Bid End Date

10-Jul-2026, 4:00 pm

Location

KOLLAM , KERALA
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Progress

Issue19-Jun-2026, 3:34 pm
AwardPending
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Quantity

1500

Bid Type

Two Packet Bid

Categories 3

BRACES FIRST AID BOX ORTHODONTIC AND PROSTHODONTIC EQUIPMENT

A tender has been published for Employees State Insurance Corporation Knee Braces and Splints (V2) (Q3) in KOLLAM, KERALA. Quantity: 1500 by. Submission Deadline: 10-07-2026 16: 00: 00. Check eligibility and apply.

Additional Tender Data

Commercial Details

Tender Category

Goods

Bid To RA

No

Bid To RA Enabled

Yes

Item Category

Knee Braces and Splints (V2) (Q3)

Authority Records

MINISTRY OF LABOUR AND EMPLOYMENT

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Documents 3

GeM-Bidding-9493520.pdf

Main Document

CATALOG-Specification-1

CATALOG Specification

GEM General Terms and Conditions Document

GEM_GENERAL_TERMS_AND_CONDITIONS

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Technical Specifications 1 Item

Item #1 Details

View Catalog
Category Specification Requirement
GENERAL Product Description Knee Braces and Splints
PRODUCT INFORMATION Product Use Knee Joint Support for immobilization
PRODUCT INFORMATION Product style Knee Cap
PRODUCT INFORMATION Features of braces and splints Flexible
PRODUCT INFORMATION Patient Type Adult
PRODUCT INFORMATION Adjustable Functionality No
PRODUCT INFORMATION Type of opening Elastic with closed patella (Knee Cap), Sleeve Type, Stretchable Elastic, Sleeve Type
PRODUCT INFORMATION Stretchability Yes
PRODUCT INFORMATION Type of Stretchability 2 way, 4 way
PRODUCT INFORMATION Material of components Knitted elastic tape
PRODUCT INFORMATION Size Small, Medium, Large, X- Large, XX- Large
Certifications & Reports Compliance to Medical Device Rule (MDR) 2017 as amended till date Yes
Certifications & Reports Availability of valid Medical Device license/Registration 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 & Reports Manufacturing unit certification ISO: 13485 (Latest)
Certifications & Reports Availability of Test Report for each supplied batch/product as per Medical Device Rule (MDR) 2017 as amended till date Yes
Certifications & Reports 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 (in months) 24, 30, 36, 48 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

Experience Criteria

2

Past Performance

3

Bidder Turnover

4

Certificate (Requested in ATC)

5

OEM Authorization Certificate

6

OEM Annual Turnover

7

Additional Doc 1 (Requested in ATC) *In case any bidder is seeking exemption from Experience / Turnover Criteria

8

the supporting documents to prove his eligibility for exemption must be uploaded for evaluation by the buyer

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