Sterile Hypodermic Needles for Single use (V2),Sterile Hypodermic Needles for Single use (V2)
Sabarkantha District Panchayat
SABARKANTHA, GUJARAT
Progress
Quantity
600
Bid Type
Two Packet Bid
The Directorate Of Animal Husbandry, under the Agriculture And Co-operation Department of Gujarat, invites bids for the supply of Single Use Sterile Hypodermic Syringes for Human Use conforming to IS 10258 (Part 1). The procurement location is Ahmedabad, Gujarat. The scope covers the supply of sterile syringes with needle included, adhering to the drugs act and medical device rules, with a 4000 INR EMD obligation. A key bid term is the supplier’s ability to accommodate a potential quantity variation up to 25% of the bid quantity and to supply per approved samples prior to bulk manufacture. The bid is structured as a straightforward supply contract with post-approval sample conditions and an option clause that modulates delivery timelines, ensuring compliance with regulatory and technical standards.
Product: Single Use Sterile Hypodermic Syringe with needle included
Nominal capacity: as per IS 10258 Part 1
Packaging: pack size details to be specified in BOQ
Certification: Drugs and Cosmetic Act 1940; MDR 2017; valid medical device license
Standards: IS 10258 (Part 1) compliant for human-use syringe
Quality: advance sample approval required (5 samples within 5 days)
Delivery: option clause allows 25% quantity variation
EMD ₹4,000 via DD or eligible exemption
Pre-production advance samples required within 5 days of award
Quantity adjustment up to 25% during and after contract
Compliance with Drugs and Cosmetic Act and MDR 2017
IS 10258 Part 1 certification mandatory
EMD must be submitted (₹4,000) unless exempted; payment terms follow Gujarat govt procurement policies.
Delivery period may be recalculated if quantity is increased; minimum 30 days; extension permissible within contract.
Major deviations in sample approval may lead to contract termination; LDs may apply for non-compliance.
Proven experience supplying sterile medical devices including syringes
Valid GST registration and PAN
Demonstrated compliance with IS 10258 Part 1 and MDR 2017
Sabarkantha District Panchayat
SABARKANTHA, GUJARAT
Directorate Of Purchase And Stores
Directorate Of Animal Husbandry
AHMEDABAD, GUJARAT
Directorate Of Animal Husbandry
AHMEDABAD, GUJARAT
N/a
BHAVNAGAR, GUJARAT
Tender Results
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| 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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GST certificate
PAN card
Experience certificates showing relevant supply of sterile medical devices
Financial statements for the last financial year
EMD submission receipt (₹4,000 DD) or exemption certificate
Technical bid documents demonstrating IS 10258 Part 1 compliance
OEM authorization/authorization letters from manufacturers of sterile syringes
Medical device license copy for the product from competent authority
Extended Deadline
01-Dec-2025, 7:00 pm
Opening Date
01-Dec-2025, 7:30 pm
Key insights about GUJARAT tender market
Bidders must meet eligibility criteria (experience with sterile medical devices, GST, PAN) and submit EMD ₹4,000 unless exempt. Provide IS 10258 Part 1 compliance and a valid medical device license. Include advance sample submission within 5 days of award and comply with the 25% quantity option clause.
Submit GST certificate, PAN card, experience certificates for sterile devices, financial statements, EMD proof, IS 10258 Part 1 compliance documents, OEM authorizations, and a valid medical device license. Technical bid should demonstrate regulatory compliance and sample approval readiness.
Bids must conform to IS 10258 Part 1 for single-use sterile syringes and comply with the Drugs and Cosmetic Act 1940 and Medical Device Rules (MDR) 2017. A valid medical device license from the competent authority is mandatory for the product.
EMD is ₹4,000 payable via demand draft unless exempted under Gujarat government policy. Ensure the draft is in favor of the purchasing authority and submitted with the bid as part of the technical envelope.
Delivery can be adjusted by up to 25% of bid quantity at contract placement and during the currency at contracted rates. Additional time is calculated as (Increase/Original quantity) × Original delivery period, with a minimum of 30 days from the original delivery date.
Submit 5 advance samples within 5 days of award. The buyer will approve or specify modifications within 5 days. If delayed approvals occur, delivery period adjusts accordingly without LD; major non-conformities may lead to contract termination.
Required certifications include compliance with the Drugs and Cosmetic Act 1940, MDR 2017 as amended, and a valid medical device license. Vendors must demonstrate IS 10258 Part 1 compliance for human-use syringes and provide OEM authorization if applicable.
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Main Document
CATALOG Specification
OTHER
OTHER
ATC
GEM_GENERAL_TERMS_AND_CONDITIONS
Main Document
CATALOG Specification
OTHER
OTHER
ATC
GEM_GENERAL_TERMS_AND_CONDITIONS