GEM

Gujarat Health & Family Welfare Department Hemoglobin Test Strips Tender Daodh Gujarat 2025

Posted

18 Oct 2025, 03:11 pm

Deadline

08 Nov 2025, 03:00 pm

EMD

₹29,328

Progress

Issue18 Oct 2025, 03:11 pm
AwardPending
Explore all 4 tabs to view complete tender details

Quantity

39104

Bid Type

Two Packet Bid

Key Highlights

  • Vendor must comply with MDR 2017 and Drugs and Cosmetics Act 1940 drug license
  • EMD ₹29,328 with MSE startup exemption possible via NSIC/DIC-CSPO
  • 25% quantity variation right; extended delivery period with formula and minimum 30 days
  • Advance sample submission required before commencement of supply
  • Packaging: English packing insert; storage conditions specified
  • Manufacturing unit certification required; product suitability for Hemoglobin test strips
  • BaU terms include no BOQ items; focus on single product category with compliance
  • Daohod, Gujarat location; startup exemptions under Gujarat state policy
  • Exact delivery windows tied to original vs extended delivery periods

Tender Overview

The Gujarat Health & Family Welfare Department invites bids for Hemoglobin Test Strips to be supplied to DAHOD, Gujarat (389130). The procurement involves standard medical device strips with packaging in English inserts, MDR 2017 compliance, and drug license validity. The estimated value is not disclosed, but an EMD of ₹29,328 applies. The bid emphasizes supplier qualification, sample submission prior to supply, and adherence to shelf-life requirements. A key differentiator is the option clause allowing quantity adjustments up to 25%, extending delivery time proportionally with a minimum of 30 days. This opportunity targets suppliers capable of meeting MDR and drug licensing standards and capable of world-class quality assurance. The tender is notable for its emphasis on startup/MSE exemptions from EMD, subject to NSIC/CSPO documentation.

Technical Specifications & Requirements

  • Product category: Hemoglobin Test Strips (General/Medical Devices)
  • Certifications: MDR 2017 compliance, valid drug license under Drugs and Cosmetics Act 1940, Manufacturing unit certification
  • Shelf life: minimum shelf life at delivery, shelf life after opening, and months from manufacture
  • Packaging: English packing insert with each pack; storage conditions defined
  • Advance sample: mandatory pre-supply sample for buyer approval
  • BoQ: no items listed; focus on single-line product with precise compliance expectations
  • EMD condition: ₹29,328; exemptions for MSE startups with NSIC/CSPO docs (startups under Gujarat state policy)
  • Delivery: option for quantity variation and extended timelines per clause; delivery begin from last date of original order
  • Quality/Testing: adherence to medical device rules and standard testing procedures
  • Lot considerations: no BOQ items; quantity will be governed by contract under option clause
  • Sample submission: advance sample submission required

Terms, Conditions & Eligibility

  • EMD: ₹29,328; exemptions available for MSE startups with valid NSIC/DIC certificate or CSPO documents
  • Experience/Turnover: startups may qualify for exemption; otherwise, standard eligibility applies per buyers terms
  • Delivery: delivery period adjustable within 25% quantity variation; minimum 30 days extension where applicable
  • Payment terms: not explicitly stated; reference to standard procurement terms and progressive payments
  • Documents: GST, PAN, experience certificates, financial statements, EMD submission, technical bid, OEM authorizations
  • Warranty/Support: not explicitly detailed; MDR compliance and drug license imply post-sale support expectations
  • Compliance: must meet MDR 2017 and possess valid drug license from competent authority under Drugs and Cosmetic Act 1940
  • ATC: exemption notes and circulars apply for Gujarat startups
  • Restrictions: no tender ID or dates to be mentioned; ensure compliance with option clause and EMD exemptions

Key Specifications

  • Hemoglobin Test Strips

  • MDR 2017 compliant

  • Drugs and Cosmetics Act 1940 licensed product

  • Manufacturing unit certification

  • English language packing inserts

  • Shelf-life details: manufacture date, remaining shelf life at delivery, post-opening shelf life

  • Advance sample provision prior to supply

  • Storage conditions specified

Terms & Conditions

  • EMD ₹29,328 with startup exemption possibilities

  • 25% quantity variation rights and extended delivery timelines

  • MDR 2017 and Drug License compliance required

Important Clauses

Payment Terms

Not explicitly stated; bidders should anticipate standard government terms and potential milestone payments; EMD compliance applies

Delivery Schedule

Delivery period adjustable with 25% quantity variation; minimum 30 days extension under option clause

Penalties/Liquidated Damages

Not specified; implied adherence to standard procurement penalties for delays may apply

Bidder Eligibility

  • MSE startups with NSIC/DIC-Acknowledgment part-II/CSPO certificate eligible for EMD exemption

  • Manufacturing unit certification required for compliance

  • Drug license under Drugs and Cosmetic Act 1940 valid at time of bid

Technical Specifications 1 Item

Item #1 Details

View Catalog
Category Specification Requirement
GENERAL FEATURES Product Description Hemoglobin Test Strip
PRODUCT INFORMATION Parameter Measured Hemoglobin (Hb) Level
PRODUCT INFORMATION Sample Type Whole Blood (Capillary/Venous/Arterial)
PRODUCT INFORMATION Type Reagent Free Hemoglobin Strip
PRODUCT INFORMATION Sample Size ≤50 microliters (µL)
PRODUCT INFORMATION Working Principle Absorbance Photometry
PRODUCT INFORMATION Measurement Range 0 to 23 g/dL or more Or higher
PRODUCT INFORMATION Measurement Time ≤ 60 Seconds
PACKAGING Packaging Type Vial
PACKAGING Packing Insert in English provided with each pack Yes
PACKAGING Storage Conditions 2°C-30°C
CERTIFICATIONS & REPORTS Compliance to Medical Device Rules (MDR) 2017 as amended till date Yes
CERTIFICATIONS & REPORTS Availability of valid drug license for the product issued from the competent authority defined under Drugs and Cosmetic Act 1940 and Rules made there under as amended till date Yes
CERTIFICATIONS & REPORTS Manufacturing unit certification ISO:13485 (Latest)
SHELF LIFE Shelf life in months from the date of Manufacture 24, 36 Or higher
SHELF LIFE Minimum Shelf life available at the time of delivery to the consignee 3/4th of total shelf life
SHELF LIFE Shelf life after first opening of the pack (months) Minimum 3 months or more
ADVANCE SAMPLE Agree to provide advance sample of the product for buyer's approval before commencement of supply in case of bidding Yes, No

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Required Documents

1

GST registration certificate

2

PAN card

3

Experience certificates for similar medical device supply

4

Financial statements (last 3 years)

5

EMD submission document or exemption proof

6

Technical bid/compliance certificates

7

OEM authorization letter (if applicable)

8

NSIC/DIC-Acknowledgment part-II/CSPO certificate for MSE startups (EMD exemption eligibility)

9

Drug license under Drugs and Cosmetic Act 1940 (valid)

10

Manufacturing unit certification

Frequently Asked Questions

How to bid for hemoglobin test strips tender in Daodh Gujarat 2025

Bidders must submit GST, PAN, experience certificates, financial statements, EMD ₹29,328, technical bid, OEM authorizations, and NSIC/CSPO documents if claiming MSE startup exemption. Ensure MDR 2017 compliance, valid drug license, and manufacturing unit certification. Include advance sample provision and confirm English packing inserts.

What documents are required for Gujarat health tender 2025 hemoglobin strips

Required documents include GST certificate, PAN card, last 3 years financials, experience certificates for similar supply, EMD or exemption proof, technical bid/compliance certificates, OEM authorization, drug license under Drugs and Cosmetics Act, and manufacturing unit certification. Startups must provide NSIC/DIC-CSPO proof.

What standards and licenses must hemoglobin strips meet Gujarat MDR

Product must comply with MDR 2017, have a valid drug license under the Drugs and Cosmetics Act 1940, and a manufacturing unit certification. These ensure clinical safety and regulatory compliance for medical devices supplied to Gujarat Health Department.

When is the delivery deadline for Daodh hemoglobin strips tender

Delivery terms permit a 25% quantity variation with an initial delivery period; extended delivery time is calculated as (increased quantity ÷ original quantity) × original delivery period, with a minimum extension of 30 days. Exact dates align to purchase order.

What is the EMD exemption criteria for Gujarat startups in this bid

Startups classified as MSE may be exempt from EMD if they hold valid NSIC/DIC-Acknowledgment part-II or CSPO certificate. They must submit the relevant documents along with the bid to claim exemption.

What packaging and sample requirements are specified for the strips

Each pack must include an English packing insert; advance sample must be provided before commencement of supply for buyer approval. Storage conditions should be followed as per MDR-compliant packaging guidelines.

What are the key eligibility criteria for supplier in Gujarat health tender

Eligibility includes MDR 2017 compliance, valid drug license under Drugs and Cosmetics Act, manufacturing unit certification, GST and PAN, experience in similar medical device supply, and ability to provide advance sample and maintain packaging requirements.

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