TenderDekho Logo
Closed GEM

Rail Coach Factory Kapurthala Sterile Hypodermic Syringes Tender Kapurthala Punjab IS 10258 Part 1 2026

Bid Publish Date

02-Aug-2026, 9:23 pm

Bid End Date

13-Aug-2026, 9:00 am

Progress

Issue02-Aug-2026, 9:23 pm
AwardPending

Key Highlights

  • IS 10258 (Part 1) compliance for human-use syringes
  • MDR 2017 and Drugs and Cosmetic Act 1940 compliance
  • Valid Medical Device license from competent authority required
  • Needle included with syringe; needle cap/shield for safety

Tender Overview

Rail Coach Factory Kapurthala, under Indian Railways, seeks supply of Single Use Sterile Hypodermic Syringes for Human Use conforming to IS 10258 (Part 1). The procurement scope is goods-only delivery to the Kapurthala facility in Punjab (postal code 144038). Key requirements include needle included in syringe sets, syringe type based on number of pieces, needle cap/shield, and specified nominal capacity per unit. Packaging must state number of pieces per pack and ensure a defined residual shelf life. Certifications demand compliance with the Drugs and Cosmetic Act 1940 and MDR 2017 and a valid Medical Device license. The contract involves inspection by Rail Coach Factory Kapurthala post-receipt; pre-dispatch inspection is not mandated by ATC. No BOQ items are listed, indicating a straightforward supply contract for sterile syringes subject to quality checks at delivery. The opportunity targets suppliers with medical device licensure and IS 10258 conformity. Unique aspects include site-specific acceptance and a focus on human-use sterile syringes with clear certification requirements.

  • Organization: Rail Coach Factory Kapurthala
  • Location: Kapurthala, Punjab 144038
  • Product category: Single Use Sterile Hypodermic Syringes for Human Use
  • Standards: IS 10258 (Part 1); MDR 2017; Drugs and Cosmetic Act 1940
  • Inspection: Post-receipt by consignee; pre-dispatch NA
  • Delivery scope: Goods-only; no BOQ items

Technical Specifications & Requirements

  • Needle: Included with each syringe set; ensure proper sterile packaging
  • Syringe configuration: Type determined by number of pieces per package
  • Needle protection: Include cap or shield to prevent needlestick injuries
  • Nominal capacity: Define per syringe (in ml) per unit specification
  • Packaging: Clear label of pieces per pack and batch/lot information
  • Shelf life: Residual shelf life must meet standard medical device expectations
  • Certifications: Compliance to Drugs and Cosmetic Act 1940 and Medical Device Rules (MDR) 2017 as amended; valid Medical Device license from competent authority
  • Inspection: Post-delivery inspection executed by Rail Coach Factory Kapurthala at consignee site; pre-dispatch inspection not mandated
  • Compliance expectations: All items must be sterile, human-use eligible, and IS 10258 (Part 1) compliant

Terms, Conditions & Eligibility

  • Scope: Supply of goods only; no service components
  • EMD/Security: Not disclosed in data; ensure typical bid security compliance per Railways practices
  • Delivery timeline: Not specified; align with Rail Coach Factory Kapurthala acceptance timelines
  • Payment terms: Not specified; bidders should be prepared for standard Railway payment cycles
  • Documents: GST certificate, PAN, Medical Device license, IS 10258 compliance proof, post-delivery inspection readiness
  • Qualification: Demonstrated ability to supply sterile hypodermic syringes meeting MDR and IS standards; valid medical device licensing
  • Penalties: Performance-related penalties or LD clauses not specified; bidders should anticipate standard terms
  • Warranty/AMC: Not specified; request standard device warranty terms during bid submission

Key Specifications

  • Single Use Sterile Hypodermic Syringes for Human Use

  • Needle included with syringe set

  • Syringe type determined by number of pieces per pack

  • Needle cap/shield to prevent needlestick injuries

  • Nominal capacity specified per unit (ml)

  • Packaging indicates pieces per pack

  • Residual shelf life adheres to medical device standards

  • Compliance with Drugs and Cosmetic Act 1940 and MDR 2017

  • Medical Device license valid from a competent authority

Terms & Conditions

  • Post-delivery inspection by consignee at Rail Coach Factory Kapurthala

  • Goods-only supply; no service or installation

  • IS 10258 (Part 1) and MDR 2017 compliance required

Important Clauses

Inspection

Post Receipt Inspection at consignee site; pre-dispatch inspection not specified in ATC

Delivery Schedule

Delivery timelines to be aligned with Rail Coach Factory Kapurthala acceptance process; exact days not disclosed

Payment Terms

Payment terms not specified; bidders should expect standard Railway terms

Bidder Eligibility

  • Valid Medical Device license for the syringes

  • IS 10258 (Part 1) conformity or testing evidence

  • Experience in supplying sterile hypodermic syringes for human use

Authority & Contact

Department

Indian Railways

Office Name

Kapurthala

Grievance Contact

[email protected]

Tender Data

Bid Details

Quantity

360

Bid Type

Single Packet Bid

Bid Validity

90 (Days)

Bid Type

Service

Evaluation

Total value wise evaluation

Inspection Required

No

Tech Clarification Time

2 Days

Preference & Exemptions

EMD Required

No

MII Purchase Preference

No

MSE Purchase Preference

Yes

MSE Preference Band

L1+15%

MSE Exemption/Relaxation

No

Startup Exemption/Relaxation

No

Bid Splitting Applied

No

Requirements

Arbitration Clause

No

Mediation Clause

No

Additional Tender Data

Commercial Details

Tender Category

Goods

Bid To RA

No

Bid To RA Enabled

No

Item Category

Single Use Sterile Hypodermic Syringes for Human Use Conforming to IS 10258 (Part 1) (Q2)

Delivery Details

Max Delivery Days

15

Delivery Locations

1

Delivery Cities

Kapurthala

Delivery Pincodes

144602

Delivery Locations

ConsigneeAddressCityStatePincodeQuantityDelivery DaysAdditional Requirement
Rajesh Mohan144602,Cheif Medical Officer, LLR Hosipital, Kapurthala PunjabKapurthalaPunjab14460236015-

Authority Records

MINISTRY OF RAILWAYSRAIL COACH FACTORY KAPURTHALA

BID & GeM Expert Consultancy

End-to-end support — bid preparation, GeM registration, document filing & compliance by industry experts.

Bid Preparation GeM Registration Document Filing

Free consultation · 24h response

Documents 5

GeM-Bidding-9697729.pdf

Main Document

CATALOG-Specification-1

CATALOG Specification

Other Documents

OTHER

Other Documents

OTHER

GEM General Terms and Conditions Document

GEM_GENERAL_TERMS_AND_CONDITIONS

Required Documents

1

GST registration certificate

2

Permanent Account Number (PAN) card

3

Medical Device license/registration for the product

4

IS 10258 (Part 1) conformity certificate or test report

5

Experience certificates for similar procurement of sterile syringes

6

Technical bid documents confirming compliance with MDR 2017

7

Manufacturers/OEM authorization letters (if applicable)

8

Financial statements or turnover proof as required by procurement norms

9

Any pre-qualification documents requested in terms (if provided)

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) >2 - 5
PACKAGING Number of pieces in a Pack 50
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

Frequently Asked Questions

Key insights about PUNJAB tender market

How to bid for IS 10258 Part 1 syringes tender in Kapurthala

Bidders must provide IS 10258 Part 1 conformity proof, valid Medical Device license, GST, PAN, and experience certificates for similar sterile syringe supply. Include post-delivery inspection readiness and confirm needle-included syringes with safety caps. Delivery terms align with Rail Coach Factory inspection requirements and payment terms per Railway norms.

What documents are required for Kapurthala syringe procurement

Submit GST certificate, PAN, Medical Device license, IS 10258 conformance evidence, OEM authorization if applicable, and experience certificates for sterile medical device supply. Include financial statements, product specification sheets, and post-delivery inspection readiness documentation to meet Railways procurement standards.

What are the technical specifications for IS 10258 syringes in this tender

Syringes must be sterile and human-use compliant with IS 10258 Part 1, include a needle and needle shield, have defined nominal capacity (ml), and packaging indicating pieces per pack and batch information. Compliance with MDR 2017 and Drugs and Cosmetic Act 1940 is mandatory for qualification.

What is the inspection process for delivery to Kapurthala facility

Post-receipt inspection will be conducted by Rail Coach Factory Kapurthala at the consignee site. Pre-dispatch inspection is not mandated by ATC. Suppliers should ensure ready-to-inspect stock, proper labeling, and batch traceability for quick acceptance.

What are the certification requirements for the syringes

Syringes must comply with MDR 2017 and Drugs and Cosmetic Act 1940, plus a valid Medical Device license. Documentation should include license number, issuing authority, and validity dates, along with IS 10258 compliance evidence to prove product eligibility.

What are the delivery and payment expectations for this bid

Delivery timelines are aligned with consignee acceptance requirements; exact delivery days are not disclosed. Payment terms are not specified publicly; bidders should anticipate standard Railway payment cycles after successful delivery and inspection completion, with documentation supporting acceptance.