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National Rural Health Mission Gujarat Sterile Hypodermic Syringes Tender Ahmedabad 2026 IS 10258 Part 1 MDR 2017

Bid Publish Date

04-Jul-2026, 4:34 pm

Bid End Date

14-Jul-2026, 5:00 pm

Progress

Issue04-Jul-2026, 4:34 pm
AwardPending
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Quantity

1500

Bid Type

Two Packet Bid

Categories 2

Tender Overview

The National Rural Health Mission (NRHM) State Health Society, Gujarat invites bids for single-use sterile hypodermic syringes conforming to IS 10258 (Part 1) for human use, to be procured in AHMEDABAD, GUJARAT. Key product features include syringes with an integrated needle, a protective needle cap/shield, and a specified nominal capacity (ml). Compliance with the Drugs and Cosmetic Act 1940 and Medical Device Rules (MDR) 2017 is mandatory, with a valid medical device license required from the competent authority. Bidders should anticipate a procurement framework with sample approvals and a state-level preference for MSEs under the Udyam regime. The option clause allows quantity variations up to 25% of bid quantity during contract execution, potentially extending delivery time with calculated adjustments. This tender emphasizes regulatory conformity, sample-based verification, and supplier readiness for bulk manufacturing after approval. Competitive bids will hinge on standard-compliant supply, timely delivery, and adherence to option-clauses and sample approvals.

Technical Specifications & Requirements

  • Product information: Syringe with needle included; needle shield/cap; category: single-piece/bulk depending on packaging; Nominal capacity in ml to be specified in BOQ.
  • Packaging and shelf life: Pack size and residual shelf life requirements to be confirmed; ensure minimal regulatory risk.
  • Certifications: Drugs and Cosmetic Act 1940 compliance; MDR 2017 (as amended); valid Medical Device license from competent authority.
  • Quality controls: Conformity to medical device standards; sample approval process prior to bulk manufacturing; advance samples due within 5 days of award; LD/penalties to be as per contract for deviations.
  • Delivery readiness: Ready-to-supply after sample approval; option clause may adjust quantities and delivery timing; evaluation will consider regulatory compliance and sample conformity.

Terms, Conditions & Eligibility

  • EMD/SECURITY: Details not stated; anticipate standard tender security as per local norms.
  • Delivery timelines: Delivery period linked to original order date with potential extension under the option clause; additional time calculated and minimum 30 days.
  • Purchase preference: State-level preference for MSEs with valid Udyam Registration.
  • Documentation: Compliance with buyer-specified terms; advance sample approval process; bulk supply only after approval.
  • Payment terms: To be defined in contract; anticipate standard government procedures for medical devices.
  • Other terms: General procurement safeguards, conformity to regulatory licenses, and adherence to bid conditions.

Key Specifications

  • Single-use sterile hypodermic syringes conforming to IS 10258 (Part 1)

  • Needle included with syringe; needle shield/cap provided

  • Nominal capacity to be specified (ml)

  • Packaging: number of pieces per pack to be defined

  • Residual shelf life to be stated

  • Regulatory: Drugs and Cosmetic Act 1940 and MDR 2017 compliance

  • Licensing: valid Medical Device license from competent authority

Terms & Conditions

  • EMD amount and submission method to be clarified in tender documents

  • Delivery terms allow 25% quantity variation with adjusted delivery period

  • Advance sample approval required within 5 days post-award; bulk supply after approval

Important Clauses

Payment Terms

Payment terms to be specified in contract; likely government-standard with possible mobilization advances after approval

Delivery Schedule

Delivery period linked to original order date; extension calculated as (additional quantity/original quantity) × original delivery period, minimum 30 days

Penalties/Liquidated Damages

Damages for non-conformity or delayed supply to be defined in contract; sample deviations may lead to termination

Bidder Eligibility

  • Authorized to supply sterile medical devices in Gujarat

  • Demonstrated MDR 2017 and Drugs and Cosmetic Act compliance

  • Valid Medical Device license for the product

  • MSEs from Gujarat eligible for state purchase preference

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

HEALTH AND FAMILY WELFARE DEPARTMENT

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Documents 6

GeM-Bidding-9557519.pdf

Main Document

CATALOG-Specification-1

CATALOG Specification

Other Documents

OTHER

Other Documents

OTHER

Buyer uploaded ATC document

ATC

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
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) 3
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 medical device supply

4

Financial statements (last 2-3 years)

5

EMD/Security deposit as prescribed

6

Technical bid documents demonstrating MDR 2017 compliance

7

OEM authorization (where applicable)

8

Medical Device license copies and regulatory approvals

9

Manufacturing/quality certificates and ISI/ISO where applicable

Frequently Asked Questions

Key insights about GUJARAT tender market

How to bid for the sterile syringe tender in Ahmedabad Gujarat 2026?

Bidders must meet eligibility criteria for NRHM Gujarat, submit GST, PAN, experience certificates, financials, EMD, and MDR 2017 compliance documents. Provide Medical Device license copies, OEM authorizations if applicable, and advance sample submissions within 5 days of award. Ensure IS 10258 Part 1 conformity.

What documents are required to participate in the NRHM bid in Gujarat?

Required documents include GST registration, PAN, experience certificates for similar supply, financial statements, EMD, technical compliance certificates showing MDR 2017 compliance, Medical Device license, OEM authorization, and manufacturing quality certificates. Submit with the technical bid as per Terms.

What standards must the syringes meet for this Gujarat tender?

Syringes must conform to IS 10258 (Part 1) for human use and be compliant with Drugs and Cosmetic Act 1940 and MDR 2017. A valid Medical Device license is required, and suppliers must pass advance sample approval before bulk production.

When is advance sample approval required for the NRHM Gujarat bid?

Advance samples must be submitted within 5 days of contract award; the buyer provides modifications within 5 days. If delayed by the buyer, delivery is adjusted without LD. Bulk supply proceeds only after approval and conformity to the approved sample.

What is the quantity variation permitted under the option clause?

The Purchaser may increase or decrease the quantity up to 25% of the bid quantity at contract placement and during currency at contracted rates. Delivery time adjusts based on the formula provided, with a minimum 30 days extension rule.

What is required for MSEs seeking state purchase preference in Gujarat?

MSEs must have valid Udyam Registration and be registered in Gujarat with credentials online validated. Eligible suppliers receive state-level purchase preference as per Public Procurement Policy for MSEs 2012, enhancing bid competitiveness.

What licenses and regulatory approvals are essential for this syringe procurement?

A valid Medical Device license for the product from the competent authority is essential, along with compliance to Drugs and Cosmetic Act 1940 and MDR 2017. Bidders should provide copy of license and MDR compliance certificates in the bid.

What delivery terms apply if the original delivery period is short?

If the original delivery period is less than 30 days, the additional time equals the original period; the calculated extension applies up to the original period. The extension can be used while exercising the option clause to adjust delivery.

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