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Andaman & Nicobar Health Department Single Use Sterile Hypodermic Syringes Tender IS 10258 2017 MDR 2017 2026

Bid Publish Date

15-Feb-2026, 8:39 pm

Bid End Date

02-Mar-2026, 4:00 pm

EMD

₹39,000

Progress

Issue15-Feb-2026, 8:39 pm
AwardPending
Explore all 4 tabs to view complete tender details

Quantity

10000

Category

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

Bid Type

Two Packet Bid

Categories 2

Tender Overview

The Government Health Department of Andaman & Nicobar, South Andaman (744101) seeks supply of Single Use Sterile Hypodermic Syringes for Human Use conforming to IS 10258 (Part 1). The procurement covers syringes with needles, needle shields, and standard packaging, aligned to the MDR 2017 framework. The project requires an EMD of ₹39,000 and mandates a valid Medical Device license. Bidders must demonstrate three years of prior government procurement experience and OEM authorization if acting as an authorized distributor. The contract includes strict compliance with central and state government norms and non-assignment terms. This opportunity targets suppliers with a proven track record in government health equipment supply and experience in similar category products.

Technical Specifications & Requirements

  • Product information: Syringe with needle included; syringe type based on number of pieces; needle cap/shield to protect the needle; Nominal Capacity in ml; pack size (number of pieces per pack); ensure residual shelf life is adequate for hospital use.
  • Certifications & licenses: Compliance with the Drugs and Cosmetic Act 1940 and Medical Device Rules (MDR) 2017; valid Medical Device license from the competent authority.
  • Documentation alignment: Ensure packaging and labeling meet regulatory standards; provide proof of license and conformity with MDR 2017 amendments.
  • Quality considerations: Sterility, packaging integrity, and traceability documentation to support hospital procurement.
  • Supplier requirements: OEM authorization wherever applicable; adherence to nationwide supply standards for government tenders.
  • Note: No BOQ items are published; bid should align to product category and regulatory requirements.

Terms, Conditions & Eligibility

  • EMD: ₹39,000, payable via DD or fixed deposit receipt; submission by bank with bidder bid documents.
  • Experience criteria: Minimum of 3 years manufacturing/supplying similar category products to Central/State Govt or PSUs; attach contracts to prove annual quantities supplied.
  • Manufacturer authorization: If bidding as distributor, provide OEM authorization detailing name, address, email, and phone.
  • Contract risk & termination: Buyer may terminate for non-compliance, delivery failures, insolvency, or misrepresentation; sub-contracting requires prior consent.
  • Payment/Delivery terms: EMD submission with bid and hardcopy delivery within 5 days post bid opening; terms relative to delivery schedule will be as per final contract.
  • Legal/compliance: Ensure proper GST/PAN documentation and compliance with government procurement norms; non-assignment provisions apply.

Key Specifications

  • Needle included with syringe

  • Syringe type defined by number of pieces

  • Needle cap/shield for protection

  • Nominal capacity of syringe in ml

  • Pack size (pieces per pack)

  • Residual shelf life specification

  • Compliance with Drugs and Cosmetic Act 1940 and MDR 2017

  • Valid Medical Device license from competent authority

Terms & Conditions

  • EMD of ₹39,000 via DD/FD; submission with bid and hardcopy within 5 days

  • 3 years govt procurement experience required; attach relevant contracts

  • OEM authorization required if bidding as distributor; provide complete details

  • Contract termination allowed for non-compliance or delivery failures

  • Delivery schedule to be defined in contract; non-assignment terms apply

  • Regulatory compliance: Drugs and Cosmetic Act and MDR 2017; valid medical device license

Important Clauses

Payment Terms

EMD to be submitted as DD/FD; payment terms to be defined in the final contract; provide scanned proof with bid

Delivery Schedule

Delivery timeline to be specified in contract; supplier liable for timely delivery and replacement of defective items

Penalties/Liquidated Damages

Buyer may terminate for non-compliance, delivery delays, or misrepresentation; performance guarantees apply

Bidder Eligibility

  • 3 years of government or PSUs experience in supplying similar category syringes

  • OEM authorization or manufacturer affiliation for distributors

  • Valid Medical Device license and regulatory compliance

  • Financial capability to supply required volumes and provide EMD

Documents 6

GeM-Bidding-8842813.pdf

Main Document

CATALOG-Specification-1

CATALOG Specification

CATALOG-Specification-2

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 2 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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Required Documents

1

GST Registration Certificate

2

Permanent Account Number (PAN) Card

3

Experience Certificates for similar govt supply (3+ years)

4

Contract copies of similar category supplies to Govt/PSU

5

OEM Authorization / Distributor Agreement

6

EMD submission proof (DD/FD) and scanned copy with bid

7

Medical Device license for the product (competent authority)

8

Proof of address and authorized signatory details

Frequently Asked Questions

Key insights about ANDAMAN & NICOBAR tender market

How to bid for syringe tender in Andaman & Nicobar 2026

Bidders must meet eligibility including 3 years govt supply experience, provide OEM authorization if distributor, and attach EMD ₹39,000 via DD/FD. Ensure compliance with IS 10258 and MDR 2017, and submit Medical Device license. Include all mandatory documents and hardcopy submission within 5 days post bid opening.

What documents are required for syringes tender in South Andaman

Required documents include GST, PAN, experience certificates, govt supply contracts, OEM authorization, EMD proof (DD/FD), Medical Device license, and bid submission proofs. Ensure signatory authorization and correct product compliance with IS 10258, and provide license validity details.

Which standards govern single-use sterile syringes in this bid

Syringes must conform to IS 10258 (Part 1) and comply with Drugs and Cosmetic Act 1940 along with MDR 2017 amendments. A valid Medical Device license must be demonstrated, with license issued by the competent authority prior to bid submission.

What is the EMD amount for this procurement in Andaman

The EMD required is ₹39,000, payable via Account Payee Demand Draft or Fixed Deposit Receipt. Scanned DD/FD proof must accompany the bid, with the hardcopy delivered within 5 days after bid end/opening.

What are the delivery expectations and penalties in this tender

Delivery terms will be specified in the final contract; supplier must meet timely delivery and replace defective items promptly. Penalties or termination rights exist for non-compliance, delayed delivery, or misrepresentation, with assignment and subcontracting restricted without buyer consent.

Is OEM authorization mandatory for this syringe tender in SBI allied health

Yes. If bidding as a distributor or service provider, provide OEM authorization with name, designation, address, email, and phone. This confirms official supply rights and aligns with government procurement norms for health equipment.

What licenses are needed to supply MDR 2017 medical devices in this bid

A valid Medical Device license issued by the competent authority is mandatory. The license must cover the syringe product and be current, reflecting compliance with MDR 2017 amendments to support hospital procurement.

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