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GEM

ESIC Single Use Sterile Hypodermic Syringes Tender Na, IS 10258 Compliant 2026

Bid Publish Date

02-Jun-2026, 11:12 am

Bid End Date

16-Jun-2026, 12:00 pm

Value

₹10,27,082

Location

GULBARGA , KARNATAKA

Progress

Issue02-Jun-2026, 11:12 am
AwardPending
Explore all 4 tabs to view complete tender details

Quantity

5913

Category

Single Use Sterile Hypodermic Syringes for Human Use Conforming to IS 10258 (Part 1)

Bid Type

Two Packet Bid

Key Highlights

  • Mandatory advance sample submission before technical evaluation
  • ISO 9001 certification required for bidder or OEM
  • IS 10258 (Part 1) conforming syringes with needle, shield, and packaging specs
  • Medicine & device compliance: Drugs and Cosmetic Act 1940 and MDR 2017
  • Delivery window: 15 days from PO; quantity variation up to 25% during contract
  • Supply-only scope; no installation; GeM policy adherence

Tender Overview

Employees State Insurance Corporation (ESIC) invites bids for the procurement of Single Use Sterile Hypodermic Syringes for Human Use conforming to IS 10258 (Part 1) (Q2). Estimated value is ₹1,027,082.20 with procurement scoped as a supply-only contract. Location details are not fully specified in the data, but the tender is issued under ESIC procurement norms. A key differentiator is the requirement for needle inclusion, shielded needle caps, and compliance with Indian drug and medical device regulations. The tender emphasizes standard compliance and supplier capabilities, including ISO 9001:2015 certification, and mandates advance sampling for technical evaluation. The scope also contemplates flexible quantity handling via an option to increase up to 25% of the bid quantity. Delivery terms align with PO issuance timing and GeM policy obligations, creating a concrete schedule framework for bidders.

Technical Specifications & Requirements

  • Product category: Single Use Sterile Hypodermic Syringes, human-use
  • Needle included; shielded needle cap or shield
  • Nominal capacity: stated in mL (exact value not specified in data)
  • Syringe type: based on number of pieces per set
  • Packaging: number of pieces per pack
  • Shelf life: residual shelf life requirement
  • Certifications: compliance with Drugs and Cosmetic Act 1940 and Medical Device Rules (MDR) 2017; valid Medical Device license from competent authority
  • Quality/standards: ISO 9001 certification for bidder or OEM
  • Sample requirement: advance sample mandatory for technical evaluation
  • Delivery window: delivery within 15 days of PO issuance; extension rules apply for quantity variations
  • The data repeats several times; bidders should ensure all items are covered in technical bid

Terms, Conditions & Eligibility

  • EMD: not disclosed in data; bidders should verify at bid stage
  • Delivery: 15 days post Purchase Order; option to adjust via 25% quantity variation
  • Payment terms: not specified in data; align with GeM buyer terms
  • Sample submission: advance sample required before technical evaluation
  • Qualification: ISO 9001 certification required (bidder or OEM)
  • Documentation: upload all bid documents per T&C; non-submission may lead to rejection
  • Scope: supply-only; no included installation services
  • Other clauses: GeM policy adherence; multiple PO installments may be issued

Key Specifications

  • Single Use Sterile Hypodermic Syringes for human use conforming to IS 10258 (Part 1) (Q2)

  • Needle included and shielded needle cap (protective cap/shield) requirement

  • Nominal capacity in mL as specified per item; syringe type determined by number of pieces

  • Packaging: specified number of pieces per pack; residual shelf life to be indicated

  • Certifications: Drugs and Cosmetic Act 1940; MDR 2017; valid Medical Device license

  • Bidder/ OEM must hold ISO 9001 certification

Terms & Conditions

  • Quantity may vary up to 25% of bid quantity at contract placement and during currency

  • Advance sample mandatory for technical evaluation

  • Delivery within 15 days of PO issuance; penalties per GeM policy for delays

Important Clauses

Payment Terms

Not explicitly stated; bidders should align with GeM/buyer terms; prepare for standard acceptance and invoicing on delivery

Delivery Schedule

Delivery within 15 days of Purchase Order; extended time provisions apply for quantity adjustments up to 25%

Penalties/Liquidated Damages

Late delivery charges as per GeM policy; ensure compliance with delivery timelines

Bidder Eligibility

  • Must possess ISO 9001 certification (bidder or OEM)

  • Demonstrate experience in supplying sterile medical devices or similar equipment

  • Hold valid regulatory licenses for Medical Devices under MDR 2017 and Drugs Act 1940

Additional Tender Data

Commercial Details

Tender Category

Goods

Bid To RA

No

Bid To RA Enabled

Yes

Item Category

Single Use Sterile Hypodermic Syringes for Human Use Conforming to IS 10258 (Part 1) (Q2)

Authority Records

MINISTRY OF LABOUR AND EMPLOYMENT
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Documents 9

GeM-Bidding-9293091.pdf

Main Document

CATALOG-Specification-1

CATALOG Specification

CATALOG-Specification-2

CATALOG Specification

CATALOG-Specification-3

CATALOG Specification

CATALOG-Specification-4

CATALOG Specification

CATALOG-Specification-5

CATALOG Specification

Other Documents

OTHER

Other Documents

OTHER

GEM General Terms and Conditions Document

GEM_GENERAL_TERMS_AND_CONDITIONS

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Technical Specifications 5 Items

Item #1 Details

View Catalog
Category Specification Requirement
PRODUCT INFORMATION Needle included Yes
PRODUCT INFORMATION Syringe type based on number of pieces Three Piece Syringe (Barrel and Piston, plunger and plunger stopper are two separate components of different materials)
PRODUCT INFORMATION Needle cap or shield to protect the needle Yes
PRODUCT INFORMATION Nominal Capacity of Syringe (ml) >2 - 5
PACKAGING Number of pieces in a Pack 100
SHELF LIFE Residual shelf life of the product Agree to provide residual shelf life of atleast 75% of total shelf life at the time of delivery to the consignee
CERTIFICATIONS Compliance to Drugs and Cosmetic Act 1940 and 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 Yes

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Historical Data

Required Documents

1

GST registration certificate

2

PAN card

3

Experience certificates for similar medical device supplies

4

Financial statements or turnover evidence

5

EMD/Security deposit documents (if applicable)

6

Technical bid documents demonstrating ISO 9001 and MDR compliance

7

OEM authorization / manufacturer proof

8

Medical Device license / regulatory approvals

Frequently Asked Questions

How to bid for ESIC syringes tender in India 2026?

Bidders must submit all required documents (GST, PAN, ISO 9001 certificate, medical device license) along with an advance sample for technical evaluation. Ensure IS 10258 (Part 1) compliance, and provide packaging and shelf life details. Delivery terms: 15 days from PO; quantity adjustments possible up to 25%.

What documents are required for ESIC syringe tender submission?

Required documents include GST certificate, PAN, experience certificates for medical device supplies, financial statements, EMD documents (if applicable), OEM authorization, technical compliance certificates, and valid Medical Device license. Upload all bid requirements to avoid rejection.

What are the technical specifications for IS 10258 syringes in this tender?

Syringes must include a needle, have shielded needle caps, and offer nominal capacity in mL as per item specifications. Packaging must indicate number of pieces per pack; residual shelf life must be stated. Compliance with MDR 2017 and Drugs Act 1940 is mandatory.

What is the delivery timeline after purchase order issuance?

Delivery must occur within 15 days of PO issuance. If quantities are increased up to 25% under the option clause, extended delivery calculations apply, with a minimum period aligned to the original terms.

What standards and certifications must bidders meet for ESIC syringes?

Bidders must hold ISO 9001 certification; products must comply with the Drugs and Cosmetic Act 1940 and Medical Device Rules (MDR) 2017; a valid Medical Device license from the competent authority is required for the product.

How does quantity variation affect the ESIC procurement contract?

ESIC may increase or decrease the quantity by up to 25% during contract execution. Delivery extensions and scheduling will be calculated as (increased quantity / original quantity) × original delivery period, with a minimum of 30 days.

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