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Kandla Port Trust Mercurial Sphygmomanometer Tender 2026 in Gujarat ISI MDR 2017 MDR Compliance

Bid Publish Date

01-Jan-2026, 12:45 pm

Bid End Date

12-Jan-2026, 1:00 pm

Progress

Issue01-Jan-2026, 12:45 pm
AwardPending
Explore all 4 tabs to view complete tender details

Quantity

5

Bid Type

Two Packet Bid

Key Highlights

  • IS I marked mercurial sphygmomanometer required with IS 3390 packaging
  • MDR 2017 compliance and valid drug license from Drugs and Cosmetic Act required
  • Manufacturing unit certification and batch-wise MDR test reports mandatory
  • All Gazette of India metrology requirements applicable to product specifications
  • Advance product sample must be provided before supply commencement
  • Quantity may be increased/decreased by 25% at purchase discretion
  • Delivery period adjustments use (additional quantity/original quantity) x original period, minimum 30 days
  • No BOQ items; procurement scope and quantities not specified
  • Bid submission must include OEM authorizations if applicable

Categories 11

Tender Overview

Kandla Port Trust invites bids for a Mercurial Sphygmomanometer to meet medical equipment standards. The tender specifies ISI-marked devices with MDR 2017 compliance, valid drug license, and manufacturing unit certification. Packaging must align with IS 3390 (Latest), and each batch requires test reports per MDR 2017. Advance sample provision is required for buyer approval prior to supply. Estimated value and quantity are not disclosed, but the contract demands rigorous certification and reporting ongoing throughout supply. Unique terms include optional quantity variation up to 25%, and a delivery-time formula tied to original delivery period with minimum 30 days.

Technical Specifications & Requirements

  • Product type: Mercurial Sphygmomanometer
  • Scale ranges: Lower and upper mmHg ranges to be specified
  • Cuff & accessories: Cuff material, bag size, inflating bulb material, and overall packaging as per IS 3390 (Latest)
  • Standards & certifications: ISI marked, MDR 2017 compliance, Drug license validity, manufacturing unit certification, Medical Device Rules requirement, and Metrology Gazette applicability
  • Documentation: Test reports for every batch per MDR 2017, gazette references, licenses, certifications to be submitted with bid or on delivery
  • Warranty & samples: Standard warranty; advance product sample required before supply commencement

Terms, Conditions & Eligibility

  • EMD/ Security deposit: Not disclosed in data; verify at bid stage
  • Delivery terms: Flexible delivery with option to adjust up to 25% quantity; delivery period calculated from last delivery order date
  • Payment terms: Not specified in data; confirm during bid
  • Documents: GST, PAN, drug license, MDR compliance certificates, ISI marks, manufacturing unit certification, batch test reports, OEM authorizations where applicable
  • Penalty/extendable scope: Option clause implies potential schedule adjustments; verify LD/penalties in contract
  • Advance sample: Must provide advance sample for buyer approval prior to bid completion

Key Specifications

  • Product: Mercurial Sphygmomanometer

  • IS 3390 packaging standard (Latest)

  • MDR 2017 compliance with test reports for each batch

  • ISI marked device and ISI certification requirement

  • Drug license number validity under Drugs and Cosmetic Act

  • Manufacturing unit certification

  • Metrology Gazette applicability to product

  • Advance sample requirement prior to supply

Terms & Conditions

  • Quantity may vary ±25% at contract; delivery extension rules apply

  • Bidders must provide advance sample for buyer approval

  • All MDR 2017 certifications, test reports, and licenses required at bid or delivery

Important Clauses

Payment Terms

Not specified; confirm at bid submission and contract stage

Delivery Schedule

Delivery aligned to original delivery period; extended period calculated as (additional quantity/original quantity) × original delivery period, minimum 30 days

Penalties/Liquidated Damages

Not specified; verify LD provisions during final contract

Bidder Eligibility

  • Proven experience in supplying medical devices or portable diagnostic equipment

  • Demonstrated MDR 2017 compliance with batch testing

  • Valid drug license under Drugs and Cosmetic Act 1940 and related amendments

Documents 4

GeM-Bidding-8781623.pdf

Main Document

CATALOG-Specification-1

CATALOG Specification

Other Documents

OTHER

GEM General Terms and Conditions Document

GEM_GENERAL_TERMS_AND_CONDITIONS

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Technical Specifications 1 Item

Item #1 Details

View Catalog
Category Specification Requirement
GENERAL Product Description Mercurial Sphygmomanometer
STANDARD Conformity to Standard IS 3390 (Latest) (Copy Attached)
STANDARD ISI Marked Product Yes
PRODUCT INFORMATION Type of Mercurial Sphygmomanometer Type 1 - Portable
PRODUCT INFORMATION Lower Scale Range (in mmHg) 0 mmHg
PRODUCT INFORMATION Upper Scale range (in mmHg) 260 to 300 mmHg
PRODUCT INFORMATION Sizes of bag Arm, adult, Arm, child
PRODUCT INFORMATION Cuff Material Cotton
PRODUCT INFORMATION Material of Inflating bulb Natural Rubber
PACKING & MARKING Packaging & Marking of Mercurial Sphygmomanometer shall be as per IS 3390 (Latest) Yes
CERTIFICATIONS Compliance to Medical Device Rules (MDR) 2017 as amended till date Yes
CERTIFICATIONS Availability of valid drug license number 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 Manufacturing unit certification ISO:13485 (Latest)
CERTIFICATIONS Availability of Test Report for each supplied batch/product as per Medical Device Rule (MDR) 2017 as amended till date Yes
CERTIFICATIONS All the Gazette of India related to legal Metrology issued from time to time, are applicable to the specification as well as to the product Yes
CERTIFICATIONS Submission of all necessary certifications, licenses and test reports to the buyer at the time of bid submission or along with supplies as per buyer requirement Yes
WARRANTY Standard Warranty 5.0, 1.0
ADVANCE SAMPLE Agree to provide advance sample of the product for buyer's approval before commencement of supply in case of bidding No, Yes

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Required Documents

1

GST registration certificate

2

Permanent Account Number (PAN)

3

Experience certificates for similar medical device supply

4

Financial statements or balance sheet

5

EMD/Security deposit as applicable (amount not disclosed)

6

Technical bid documents demonstrating MDR 2017 compliance

7

ISI certification and ISI mark details

8

MDR test reports for each batch

9

Drug license issued under Drugs and Cosmetic Act 1940

10

Manufacturing unit certification

11

Metrology Gazette compliance documents

12

Advance sample submission for buyer approval

Frequently Asked Questions

Key insights about GUJARAT tender market

How to bid for the mercurial sphygmomanometer tender in Gujarat

Bidders should ensure MDR 2017 compliance, ISI marking, and a valid drug license. Submit batch test reports, manufacturing unit certification, and IS 3390 packaging details with the bid. Include advance sample for buyer approval and confirm quantity adjustment terms (±25%).

What documents are required for mercurial sphygmomanometer bid in Kandla

Submit GST certificate, PAN, MDR test reports per batch, ISI certification, drug license, manufacturing unit certification, metrology gazette references, OEM authorizations if applicable, and advance sample for approval prior to supply.

What are the MDR 2017 compliance requirements for this tender

Provide Medical Device Rules 2017 compliance documents, batch-wise MDR test reports, and Proof of manufacturing due diligence. Ensure the device meets MDR guidelines before bid submission and during supply, with metrology certificates where applicable.

When is the delivery deadline after bid award for this tender

Delivery timing follows the last delivery order date with an option to extend; additional time is calculated as (additional quantity/original quantity) × original delivery period, minimum 30 days, with extended period allowed.

What is the packaging standard for mercurial sphygmomanometers

Packaging must conform to IS 3390 (Latest). This includes proper labeling, protective packaging for medical devices, and compliance with metrology and packaging guidelines in the tender terms.

What certifications are mandatory for bidding on this procurement

Mandatory certifications include ISI marking, MDR 2017 compliance with batch test reports, drug license under the Drugs and Cosmetic Act, and manufacturing unit certification; Gazette of India metrology references must be applicable.

What is required for advance sample submission in this bid

Bidders must agree to provide an advance sample of the mercurial sphygmomanometer for buyer approval prior to commencing supply; ensure sample meets ISI, MDR, and packaging requirements for evaluation.

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