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Contract Bidding Open For Hernia Mesh (V2) in MADURAI, TAMIL NADU

Bid Publish Date

11-Aug-2026, 1:34 pm

Bid End Date

04-Sep-2026, 2:00 pm

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Progress

Issue11-Aug-2026, 1:34 pm
Corrigendum28-Aug-2026
AwardPending

A tender has been published for N/a Hernia Mesh (V2) (Q2) in MADURAI, TAMIL NADU. Quantity: 10 by. Submission Deadline: 04-09-2026 14: 00: 00. Check eligibility and apply.

Tender Data

Bid Details

Quantity

10

Bid Type

Two Packet Bid

Bid Validity

180 (Days)

Bid Type

Service

Evaluation

Total value wise evaluation

Inspection Required

No

Tech Clarification Time

2 Days

Preference & Exemptions

EMD Required

No

MII Purchase Preference

No

MSE Purchase Preference

No

MSE Exemption/Relaxation

No

Startup Exemption/Relaxation

No

Bid Splitting Applied

No

Requirements

Min. Avg. Annual Turnover

89

OEM Avg. Turnover

7

Past Performance

30 %

Experience Required

3 Year (s)

Arbitration Clause

No

Mediation Clause

No

Additional Tender Data

Commercial Details

Tender Category

Goods

Bid To RA

No

Bid To RA Enabled

No

Item Category

Hernia Mesh (V2) (Q2)

Payment Timelines

Payments shall be made to the Seller within 45 days of issue of consignee receipt-cum-acceptance certificate (CRAC) and on-line submission of bills (This is in supersession of 10 days time as provided in clause 12 of GeM GTC)

Delivery Details

Max Delivery Days

15

Delivery Locations

1

Delivery Cities

Madurai

Delivery Pincodes

625018

Delivery Locations

ConsigneeAddressCityStatePincodeQuantityDelivery DaysAdditional Requirement
Jeyalakshmi Rani S625018,ESI HOSPITAL MADURAI, THATHANERI, MADURAI 625018MaduraiTamil Nadu6250181015-

Authority Records

LABOUR AND EMPLOYMENT DEPARTMENT

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Documents 3

GeM-Bidding-9726327.pdf

Main Document

CATALOG-Specification-1

CATALOG Specification

GEM General Terms and Conditions Document

GEM_GENERAL_TERMS_AND_CONDITIONS

Authority & Contact

Organization

N/a

Office Name

Esi Directorate

Grievance Contact

[email protected]

Corrigendum Updates

2 Updates
#1

Update

28-Aug-2026

Extended Deadline

04-Sep-2026, 8:30 am

Opening Date

04-Sep-2026, 9:00 am

#2

Update

21-Aug-2026

Extended Deadline

28-Aug-2026, 8:30 am

Opening Date

28-Aug-2026, 9:00 am

Categories 1

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Historical Data

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

Technical Specifications 1 Item

Item #1 Details

View Catalog
Category Specification Requirement
GENERAL Product Description Hernia Mesh
GENERAL Sterility Sterile
PRODUCT INFORMATION Type of Mesh Dual/Composite Mesh
PRODUCT INFORMATION Mesh Material Polyester
PRODUCT INFORMATION Composition of Layer Sodium Hyaluronate (HA) + Carboxymethylcellulose (CMC) + Polyethylene Glycol (PEG), Oxidized Regenerated Cellulose based adhesion barrier, Atelocollagen Type 1 + Polyethylene Glycol + Glycerol, Polylactide-Caprolactone, Polyurethane
PRODUCT INFORMATION Construction Type Monofilament
PRODUCT INFORMATION Mesh Shape Square, Rectangular, Round, Oval
PRODUCT INFORMATION Mesh Size in cms (±0.5 cm) 10 cm x 15 cm, 15 cm x 15 cm, 10 cm (Diameter)
PRODUCT INFORMATION Availability of orientation mark to guide mesh position and fixation Yes
PRODUCT INFORMATION Burst strength in terms of abdominal pressure for health adults More than 2 Times, More than 3 Times
PRODUCT INFORMATION Introducer Tool for smooth insertion of Mesh Yes, No
PACKING Type of Packing Sterile Packing
CERTIFICATIONS Compliance to Medical Device Rules (MDR) 2017 as amended till date Yes
CERTIFICATIONS Availability of valid medical device license 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 Manufacturer Facility Certification ISO:13485 (Latest)
CERTIFICATIONS Availability of Test Report for each supplied batch/product as per Medical Device Rules (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 and/or along with supplies as per buyer requirement Yes
SHELF LIFE Shelf life in months from the date of manufacture 60 Or higher
ADVANCE SAMPLE Agree to provide advance sample of the product for buyer's approval after award of contract and before commencement of supply in case of bidding only Yes