GEM

Directorate Of Animal Husbandry Gujarat Hypodermic Syringes Tender AHMEDABAD IS 10258 Part 1 2026

Bid Publish Date

03-Jan-2026, 5:17 pm

Bid End Date

13-Jan-2026, 6:00 pm

Progress

Issue03-Jan-2026, 5:17 pm
AwardPending
Explore all 4 tabs to view complete tender details

Quantity

600

Bid Type

Two Packet Bid

Key Highlights

  • Regulatory compliance: Drugs and Cosmetic Act 1940, MDR 2017, and valid Medical Device license
  • IS 10258 (Part 1) Q2 conformity required for all syringes with needle included
  • EMD: ₹4,000 via DD; exemption only per Gujarat government policy
  • Option clause allows ±25% quantity variation during and after contract
  • Advance sample approval: 2 samples within 5 days of award; bulk supply only per approved sample
  • Only supply of goods; no installation services; delivery timelines tied to sample approval
  • Ahmedabad, Gujarat location; bid must meet regulatory sample and licensing requirements
  • Packaging and nominal capacity details are to be aligned with IS 10258 specifications

Categories 2

Tender Overview

The Directorate Of Animal Husbandry (Gujarat) seeks Single Use Sterile Hypodermic Syringes for Human Use conforming to IS 10258 (Part 1), Q2. The procurement is focused in AHMEDABAD, GUJARAT and requires needle-included syringes, with specified nominal capacity and packaging details. The contract includes an EMD of ₹4,000 via DD and a buyer-driven option to adjust quantities by up to 25%, at contracted rates. Advance sample approval is mandatory: the supplier must submit 2 samples within 5 days of award for buyer verification; bulk supply must align with approved sample. The scope is limited to supply of goods with no installation or services, and a robust sample-alignment process governs delivery timelines if approvals lag. Bidders must comply with the buyer’s option clause and ensure supply strictly per the approved sample to avoid LD or contract termination. This tender emphasizes compliance with regulatory licensing and drug device rules, signaling strong governance in medical device procurement.

Technical Specifications & Requirements

  • Product category: Single Use Sterile Hypodermic Syringes for human use, with needle included
  • Nominal capacity: provided in tender data (ml not specified here); syringes must be compatible with ordinary medical usage
  • Packaging: number of pieces per pack as per BoQ/terms (not disclosed in data)
  • Certifications: compliant with the Drugs and Cosmetic Act 1940 and Medical Device Rules 2017; possess valid Medical Device license issued by competent authority
  • Quality/Standards: must be IS 10258 (Part 1) Q2 compliant, and maintain traceability from manufacturing to delivery
  • Brand/OEM specifics: no explicit brand lock; emphasis on regulatory compliance and sample conformity
  • Delivery/Testing: advance sample approvals required; 5-day window; LD rules may apply if approvals delay
  • EMD/Documentation: EMD ₹4,000 by DD; all relevant licenses and registrations to be submitted

Terms, Conditions & Eligibility

  • EMD: ₹4,000 via Demand Draft; exemptions only as per Gujarat Government policy
  • Delivery terms: delivery period linked to contract after sample approval; extended delivery time mechanisms exist under option clause
  • Sample requirement: submit 2 samples within 5 days of award; bulk supply must follow approved sample; non-conformity can lead to termination
  • Scope: Bid price to include all cost components; scope limited to supply of goods (no services)
  • Regulatory licenses: must hold valid Medical Device license for the product
  • Compliance: adherence to Drugs and Cosmetic Act 1940 and MDR 2017 amendments; IS 10258 (Part 1) Q2 compliance
  • Purchase policy: option to increase/decrease quantity by up to 25% during contract period
  • Payment terms: not explicitly defined in data; typically governed by standard Govt terms for medical device supply

Key Specifications

  • Product: Single Use Sterile Hypodermic Syringes for human use

  • Needle included in syringe configuration

  • IS 10258 (Part 1) compliance, Q2 quality category

  • Medical Device license (valid) required

  • Drugs and Cosmetic Act 1940 and MDR 2017 compliance

Terms & Conditions

  • EMD ₹4,000 via DD; Gujarat government policies may provide exemptions

  • Quantity variation allowed up to 25% during and after contract

  • Advance sample approval required; 2 samples within 5 days of award

  • Delivery tied to sample approval; potential LD if approvals delay

  • Regulatory licensing and IS 10258 compliance mandatory

Important Clauses

Payment Terms

EMD ₹4,000 via DD; payment terms follow government procurement norms; no explicit percentage-based advance disclosed

Delivery Schedule

Delivery begins after approved sample; option to extend as per 25% quantity variation clause; minimum 30-day scaling logic applies if extended

Penalties/Liquidated Damages

LD provisions may apply if delivery is delayed beyond approved sample-based schedule; exact LD rate not specified in data

Bidder Eligibility

  • Must hold valid Medical Device license for sterile hypodermic syringes

  • Experience in supplying similar medical devices to government or large institutions

  • Comply with IS 10258 (Part 1) Q2 and Drugs and Cosmetic Act MDR 2017 requirements

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Technical Specifications 1 Item

Item #1 Details

View Catalog
Category Specification Requirement
PRODUCT INFORMATION Needle included No
PRODUCT INFORMATION Nominal Capacity of Syringe (ml) >2 - 5
PACKAGING Number of pieces in a Pack 100
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 (as applicable to bidding entity)

5

EMD document (DD) for ₹4,000

6

Medical Device license validity for the product

7

Certificate of compliance with Drugs and Cosmetic Act 1940 and MDR 2017

8

OEM authorization (if applicable) and product technical specifications

Frequently Asked Questions

Key insights about GUJARAT tender market

How to bid for syringes tender in Ahmedabad Gujarat 2026

Bidders must submit GST, PAN, EMD ₹4,000 via DD, and medical device license. Provide IS 10258 (Part 1) Q2 compliance and 2 advance samples within 5 days of award. Follow sample-based approval and delivery timelines, with option to adjust quantity by up to 25%.

What documents are required for IS 10258 syringes tender in Gujarat

Prepare GST certificate, PAN, experience certificates for similar supply, financial statements, Medical Device license, Drug & Cosmetic Act MDR 2017 compliance, OEM authorizations if applicable, and the EMD DD of ₹4,000. Ensure items meet IS 10258 (Part 1) Q2 standards.

What are the essential standards for these syringes procurement in Gujarat

Bidders must ensure compliance with IS 10258 (Part 1) Q2, plus regulatory licensing under the Drugs and Cosmetic Act 1940 and MDR 2017. A valid Medical Device license is mandatory for the product, with sample approvals prior to bulk manufacture.

When does sample approval influence delivery for this tender

Two advance samples must be submitted within 5 days of award. Delivery is governed by the approved sample; if approval delays occur, the delivery period is adjusted without LD, according to the clause schedule and 25% quantity variation policy.

What is the EMD amount and payment terms for bidders

EMD is ₹4,000 via Demand Draft. Payment terms align with government norms; the data does not specify exact milestones, but late payments typically follow standard government procurement practice after receiving compliant deliverables and invoice verification.

What is the scope of supply in this Gujarat tender

Scope limited to supply of goods only, no installation. Bid price must include all components. The contract allows up to 25% quantity variation during and after award, with delivery timelines tied to the sample approval process.

Which licenses must be provided with the bid for medical devices

Provide a valid Medical Device license for the product from the competent authority, plus registration under the Drugs and Cosmetic Act 1940 and MDR 2017 amendments. Lob must demonstrate IS 10258 (Part 1) Q2 compliance for syringes.

What is the location and organization for this procurement

Procurement is managed by the Directorate Of Animal Husbandry under the Gujarat Agriculture and Cooperation Department, located in Ahmedabad, Gujarat. The tender focuses on sterile hypodermic syringes conforming to IS 10258 (Part 1) Q2 for human use.

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