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Employees State Insurance Corporation Sterile Hypodermic Syringes Tender Rajasthan IS 10258 (Part 1) 2026

Bid Publish Date

25-Apr-2026, 1:24 pm

Bid End Date

21-May-2026, 4:00 pm

Location

Generate Docs

Progress

Issue25-Apr-2026, 1:24 pm
Corrigendum16-May-2026
AwardPending
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Quantity

2000

Category

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

Bid Type

Two Packet Bid

Categories 2

Tender Overview

Employees State Insurance Corporation invites bids for Single Use Sterile Hypodermic Syringes for Human Use conforming to IS 10258 (Part 1) Q2. The scope includes syringes with a needle included, variable syringe pieces, and a nominal capacity in ml, packaged as a pack quantity with specified residual shelf life. Key certifications include Drugs and Cosmetic Act 1940 and Medical Device Rules (MDR) 2017 compliance, plus a valid Medical Device license. The tender permits quantity adjustments up to 25% in original and during currency at contracted rates. Location details are not specified in the data. The procurement emphasizes regulatory conformity, data-sheet verification, and OEM authorization where applicable, highlighting a data sheet match requirement and supplier integrity checks. The unique aspect is the combination of regulatory certifications and the option clause enabling flexible ordering while maintaining delivery discipline.

Technical Specifications & Requirements

  • Needle included and needle cap/shield for protection
  • Syringe type based on number of pieces and nominal capacity (ml) clearly defined
  • Packaging: number of pieces in a pack; ensure packaging integrity
  • Shelf life: specify residual shelf life; minimum usable shelf life at supply date
  • Certifications: Drugs and Cosmetic Act 1940; Medical Device Rules (MDR) 2017; valid Medical Device license from competent authority
  • Additional data: product data sheet alignment; OEM authorization if required
  • Tender requires compliance with IS 10258 (Part 1) Q2 standards and related regulatory norms

Terms, Conditions & Eligibility

  • EMD details not disclosed in the provided data; bidders should refer to tender terms for exact amount
  • Experience: bidder or OEM must have supplied similar Category Products to Central/State Govt/PSU for 2 years prior to bid opening; submit relevant contracts
  • Delivery terms: delivery period begins from last date of original delivery order; option clause allows up to 25% quantity variation and extended timing with a minimum of 30 days extra
  • Payment terms: GST as applicable; reimbursement aligned to actuals or quoted rate; ensure data-sheet alignment and avoid mismatches
  • Compliance with data sheet, OEM authorization, and shelf-life requirements (minimum 24 months shelf life; at least 18 months usable at supply date) are mandatory
  • All required submission documents per terms must be provided to participate

Key Specifications

  • Needle included

  • Syringe type based on number of pieces

  • Needle cap or shield to protect the needle

  • Nominal Capacity of Syringe (ml)

  • Number of pieces in a Pack

  • Residual shelf life of the product

  • Compliance to Drugs and Cosmetic Act 1940 and MDR 2017

  • Available Medical Device license from competent authority

Terms & Conditions

  • Quantity variation up to 25% during contract at contracted rates

  • Delivery timeline starts from last date of original delivery order

  • Minimum shelf life: 24 months; usable shelf life at supply: 18+ months

Important Clauses

Payment Terms

GST applicability; reimbursement as per actuals or contracted GST rate; ensure data-sheet match

Delivery Schedule

Delivery period begins after original delivery order; option to extend with increased quantity as per clause

Penalties/Liquidated Damages

LD terms not specified in data; refer to governing tender terms and delivery penalties if applicable

Bidder Eligibility

  • 2 years of regular manufacturing/supply of same or similar category products to Govt/PSU

  • Non-liquidation and non-bankruptcy status; solid financial undertaking

  • OEM authorization or manufacturer submission where applicable

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 11

GeM-Bidding-9258497.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

CATALOG-Specification-6

CATALOG Specification

CATALOG-Specification-7

CATALOG Specification

Other Documents

OTHER

Other Documents

OTHER

GEM General Terms and Conditions Document

GEM_GENERAL_TERMS_AND_CONDITIONS

Technical Specifications 7 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
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

PAN card

3

Experience certificates showing 2 years of supply to Govt/PSU (or OEM/authorized reseller contracts)

4

Financial statements / proof of financial standing

5

Data Sheet of the offered product(s)

6

OEM Authorization / Manufacturer's Certificate (where applicable)

7

EMD documents as per tender terms

8

Medical Device license (valid, from competent authority)

9

Any other statutory registrations requested (if specified in Terms)

Corrigendum Updates

3 Updates
#1

Update

16-May-2026

Extended Deadline

21-May-2026, 4:00 pm

Opening Date

21-May-2026, 4:30 pm

#2

Update

11-May-2026

Extended Deadline

16-May-2026, 4:00 pm

Opening Date

16-May-2026, 4:30 pm

#3

Update

05-May-2026

Extended Deadline

11-May-2026, 4:00 pm

Opening Date

11-May-2026, 4:30 pm

Frequently Asked Questions

Key insights about BIHAR tender market

How to bid for ESIC syringes tender in Rajasthan 2026?

Bidders must submit GST, PAN, and data sheets; provide OEM authorization if needed; meet 2-year Govt/PSU supply experience; comply with MDR 2017 and IS 10258; include valid Medical Device license; and adhere to the 25% quantity option and 18+ months usable shelf life requirements.

What documents are required for ESIC syringe tender submission in India?

Submit GST certificate, PAN, experience contracts with Govt/PSU, financial statements, OEM authorization, data sheet, Medical Device license, and EMD as specified; ensure data-sheet match with offered product parameters to avoid rejection.

What standards and licenses are mandatory for syringe procurement?

Must comply with Drugs and Cosmetic Act 1940, Medical Device Rules MDR 2017, IS 10258 (Part 1) Q2, and hold a valid Medical Device license from the competent authority; ensure needle safety components and packaging as per standard.

What is the delivery flexibility under the ESIC tender clause?

The purchaser may increase or decrease quantity up to 25% of bid quantity at contract, with extended delivery time calculated as (additional/original) × original period, minimum 30 days, and may extend within the original delivery window.

What is the minimum shelf life requirement for offered syringes?

Product shelf life must be a minimum of 24 months; at the date of supply, a usable shelf life of at least 18 months must be available; failure to meet this may lead to bid rejection.

How is the data sheet verification performed for ESIC syringe bids?

Bidders must upload a complete product data sheet; the data sheet will be matched against offered technical parameters; any unexplained mismatch may render the bid liable for rejection; ensure IS 10258 alignment.

What is required regarding OEM authorization for ESIC tender participation?

Authorisation Form/Certificate from OEM detailing name, designation, address, email, and phone must be furnished with the bid; distributors must provide full manufacturer authorization to bid.

What are the key packaging details bidders must specify?

Specify number of pieces per pack and ensure packaging integrity; packaging must support sterile transit and comply with medical device packaging norms as per MDR 2017.