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Andaman & Nicobar Health Department Transducer Protector V2 Tender 2026 MDR 2017 ISO 9001

Bid Publish Date

15-Jul-2026, 10:46 am

Bid End Date

25-Jul-2026, 11:00 am

Progress

RA
Issue15-Jul-2026, 10:46 am
Reverse AuctionCompleted
Award26-Sep-2026, 12:24 am

Tender Overview

The Health Department Andaman & Nicobar seeks procurement of the Transducer Protector (V2) – Q2 category. Scope centers on supply of medical-grade transducer protectors, with emphasis on compliance, batch testing, and regulatory licenses. Key differentiators include adherence to the Medical Device Rules (MDR) 2017, an active Medical Device license, and batch test reports for each supplied unit. The contract contemplates supply-only scope, with advance sample approval and shelf-life verification required prior to delivery. Unique terms include option-based quantity adjustments up to 25% and delivery timing aligned to the last original order date, ensuring uninterrupted procurement for health facilities.

Technical Specifications & Requirements

  • Product categories: General product info, Sterility, Filter membrane, Size of filter, Media, Housing material (medical grade), Housing color, Connection, Packing type.
  • Certifications: Compliance to MDR 2017, valid Medical Device license under Drugs and Cosmetic Act 1940, Manufacturing unit Certification, batch test reports per MDR, and submission of all licenses/test reports at bid or supply time.
  • Shelf life: Minimum shelf life from manufacture (months) and minimum remaining shelf life at delivery.
  • Advance sample: Agreement to provide advance sample for buyer approval before supply.
  • Documentation at bid: All relevant certifications, BIS license, type test certificates, and eligibility documentation.

Key Specifications

  • Product: Transducer Protector (V2) – Q2 category

  • Certifications: MDR 2017 compliance, Medical Device license under Drugs and Cosmetic Act, Manufacturing unit Certification, batch test reports per MDR

  • Shelf life: minimum months from manufacture; minimum remaining shelf life at delivery

  • Materials: Medical-grade housing; appropriate sterility; filter membrane size/type details

  • Test/QA: Batch-wise test reports; supplier to provide certifications at bid/supply time

  • Brand/OEM: OEM authorization required if bidding via distributor

Terms & Conditions

  • Key Term 1: 25% quantity variation rights during and after contract

  • Key Term 2: 3 years govt/PSU supply experience required

  • Key Term 3: ISO 9001 certification and MDR 2017 compliance mandatory

Important Clauses

Payment Terms

Not explicitly stated; ensure alignment with buyer terms and submission of all required certificates

Delivery Schedule

Delivery period linked to last date of original delivery order; extended time proportional to quantity increase with 30-day minimum

Penalties/Liquidated Damages

Not specified; ensure bidder clarifies LD clauses for late delivery and non-conformance

Bidder Eligibility

  • 3 years of regular manufacture/supply of similar category products to central/state govt or PSU

  • ISO 9001 certified bidder or OEM

  • Authorized distributor/OEM authorization where applicable

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Authority & Contact

Organization

N/a

Office Name

Directorate Of Health Services

Grievance Contact

[email protected]

Reverse Auction Results Final Prices

These are the final prices after the reverse auction event. Prices may be lower than initial bids.

Rank Seller Final Price Item
L1CHANDANA ENTERPRISES(MII)   Under PMA Winner ₹2,77,600Item Categories : Transducer Protector (V2)
L2NEWTECH MEDICAL DEVICES PRIVATE LIMITED (MII)   Under PMA₹2,78,000Item Categories : Transducer Protector (V2)
L3VAIDIK VENTURES (MII)   Under PMA₹3,80,000Item Categories : Transducer Protector (V2)

🎉 L1 Winner

CHANDANA ENTERPRISES(MII)   Under PMA

Final Price: ₹2,77,600

Contract / Result Documents 1

Please sign in or create an account to view contract details and download result documents.

Reverse Auction Schedule

Completed

Start

01-Sep-2026, 12:00 pm

End

02-Sep-2026, 12:00 pm

Duration: 24 hours

Reverse Auction Document

✅ RA concluded. Check financial results for final rankings.

Tender Data

Bid Details

Quantity

40000

Bid Type

Two Packet Bid

Bid Validity

120 (Days)

Bid Type

Service

Evaluation

Total value wise evaluation

Inspection Required

No

RA Qualification Rule

H1-Highest Priced Bid Elimination

Tech Clarification Time

2 Days

Preference & Exemptions

EMD Required

No

MII Purchase Preference

Yes

MII Preference Band

L1+20%

MSE Purchase Preference

No

MSE Exemption/Relaxation

No

Startup Exemption/Relaxation

No

Bid Splitting Applied

No

Requirements

Min. Avg. Annual Turnover

2

OEM Avg. Turnover

3

Experience Required

3 Year (s)

Arbitration Clause

No

Mediation Clause

No

Additional Tender Data

Commercial Details

Tender Category

Goods

Bid To RA

No

Bid To RA Enabled

Yes

Item Category

Transducer Protector (V2) (Q2)

Advisory Bank

State Bank of India

ePBG Percentage

3%

ePBG Duration (Months)

8

Payment Timelines

Payments shall be made to the Seller within 45 days of issue of consignee receipt-cum-acceptance certificate (CRAC) and on-line submission of bills (This is in supersession of 10 days time as provided in clause 12 of GeM GTC)

Delivery Details

Max Delivery Days

10000

Delivery Locations

1

Delivery Cities

South Andamans

Delivery Pincodes

744104

Delivery Locations

ConsigneeAddressCityStatePincodeQuantityDelivery DaysAdditional Requirement
Manoj Das744104,Central Medical Store, Directorate of Health Services Andaman & Nicobar AdministrationSouth AndamansAndaman And Nicobar Islands744104-10000-

Authority Records

HEALTH DEPARTMENT

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 3

GeM-Bidding-9574182.pdf

Main Document

CATALOG-Specification-1

CATALOG Specification

GEM General Terms and Conditions Document

GEM_GENERAL_TERMS_AND_CONDITIONS

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Categories 6

Required Documents

1

GST registration certificate

2

Permanent Account Number (PAN) card

3

Audited financial statements for last 3 years or CA certificate on turnover

4

ISO 9001 certification documents

5

Medical Device license (for the product) under Drugs and Cosmetic Act 1940

6

BIS license and type test certificates (if applicable)

7

OEM authorization or manufacturer authorization forms

8

Batch test reports per MDR 2017 for supplied products

9

Advance sample submission plan (if required)

Technical Specifications 1 Item

Item #1 Details

View Catalog
Category Specification Requirement
GENERAL Product Description Transducer Protector
GENERAL Sterility Sterile and Non-Pyrogenic
PRODUCT INFORMATION Filter Membrane Hydrophobic Membrane
PRODUCT INFORMATION Size of Filter 0.2 micron
PRODUCT INFORMATION Media PTFE
PRODUCT INFORMATION Housing Material (Medical Grade) ABS
PRODUCT INFORMATION Housing Color Transparent
PRODUCT INFORMATION Connection Female Lure Lock / Male Lure Lock
PACKAGING Packing Type Individual Moisture Proof Packing
CERTIFICATIONS Compliance to 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 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 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
SHELF LIFE Shelf life from the date of manufacture (months) 36 Or higher
SHELF LIFE Minimum shelf life of the product at the time of delivery to the consignee 3/4 th of Total Shelf Life
ADVANCE SAMPLE Agree to provide advance sample of the product for buyer's approval before commencement of supply in case of bidding Yes

Frequently Asked Questions

Key insights about ANDAMAN & NICOBAR tender market

How to bid for transducer protector tender in Andaman NIC 2026

Bidders must meet eligibility criteria including 3 years of govt/PSU supply experience, ISO 9001 certification, MDR 2017 compliance, and provide Medical Device license. Prepare batch test reports and OEM authorizations. Submit advance sample plan, along with BIS/type test certificates, CA turnover proof, and GST/PAN with bid.

What documents are required for MDR 2017 compliant devices tender in Andaman

Submit Medical Device license under Drugs and Cosmetic Act, MDR batch test reports, ISO 9001 certificates, BIS license, type tests, OEM authorizations, audited financial statements for 3 years, GST and PAN, and experience contracts showing govt/PSU supply.

What are the delivery terms for supply of transducer protectors in this tender

Delivery aligns with the last date of original order; if quantity increases by up to 25%, extended delivery time is calculated as (Increased quantity / Original quantity) × Original delivery period, with a minimum of 30 days.

How is eligibility demonstrated for govt procurement of medical devices

Demonstrate 3 years of regular govt/PSU supply of similar products via contracts; provide copies of contracts for each year, and ensure OEM authorization if bidding through distributors; include turnover proof and ISO 9001 status.

What standards and certifications must accompany bid submissions

Required standards include MDR 2017 compliance, ISO 9001, Medical Device license under Drugs and Cosmetic Act, BIS/type test certificates, and batch test reports for each supplied lot; all must be uploaded with bid or provided at delivery.

What is required for advance sample approval in this tender

Bidder must agree to provide an advance sample for buyer approval before commencing supply; ensure sample matches MDR-compliant specifications and is accompanied by batch test documentation.

Is there a minimum turnover requirement for bidders in this procurement

Yes. The bidder must demonstrate a minimum average annual turnover over the last three years ending 31st March, supported by audited balance sheets or CA/Cost Accountant certificate; exact turnover threshold is specified in the bid document.

Where to submit regulatory licenses and test reports for bid submission

Upload all relevant licenses (Medical Device license, BIS license), ISO 9001, type test certificates, batch MDR test reports, and OEM authorization with bid; prepare to present originals or verifications to the buyer if requested.

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