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Health And Family Welfare Services Department Puducherry Platelet Agitator and Incubator (V2) Tender Karikal Puducherry 2026 MDR

Bid Publish Date

14-Mar-2026, 4:45 pm

Bid End Date

25-Apr-2026, 6:00 pm

Progress

Issue14-Mar-2026, 4:45 pm
AwardPending
Explore all 4 tabs to view complete tender details

Quantity

1

Bid Type

Two Packet Bid

Categories 9

Tender Overview

The Health And Family Welfare Services Department Puducherry invites bids for a Platelet Agitator and Incubator (V2) to be procured and deployed at Karikal, Puducherry 609601. The scope encompasses supply, installation, testing, commissioning, training of operators, and statutory clearances if required. The tender requires adherence to medical device regulations and certifications, with OEM/authorized seller involvement for post-sale support. A key differentiator is the mandatory set of MDR 2017 compliance measures and licensing prerequisites. The procurement targets a complete clinical workstation suitable for blood platelet processing, with precise reporting and monitoring capabilities.

Technical Specifications & Requirements

  • Product Name: Platelet Agitator and Incubator (V2)
  • Product Information: Material; Chamber Volume (Ltr); Capacity (Bag); Alarms; Number of Shelves; Shelves Dimesion (WDH); Speed (RPM); Temperature Range (Degree Celsius); Operating Range; Printer (Thermal Printer) (mm)
  • Electrical & Operational: Power Requirement; Phase Type
  • Warranty: Warranty in Years
  • Certifications: Compliance to Medical Device Rules (MDR) 2017 as amended till date; Valid Medical Device license under Drugs and Cosmetics Act; Certification for manufacturing unit; Test Reports per MDR 2017; Submission of certifications/licenses/test reports at bid or with supplies; Electrical Safety
  • Documentation: Upload BIS licence, type test certificate, approval certificates and other prescribed certificates with bid; post-submission documents may be required with supplies
  • Scope of Supply: Supply, Installation, Testing, Commissioning, Training of operators, and providing statutory clearances if any; optional quantity adjustments up to 25% during contract; OEM/importer support requirements in India for after-sales service
  • Eligibility: 1 year minimum experience manufacturing/supplying similar products to Central/State Govt or PSU; no liquidation or bankruptcy status; GST considerations not binding on bid price; obsolescence not permissible

Terms & Eligibility

  • EMD: not disclosed in the provided data; bidders should expect standard EMD submission per tender documents
  • Delivery: delivery timelines and penalties to be defined in official bid documents; option clause allows +/- 25% quantity variation
  • Payment: terms not disclosed in the extract; typical government terms apply per contract
  • Documents: GST registration, PAN, experience certificates, financial statements, OEM authorizations, technical compliance certificates, and relevant MDR certifications
  • Warranty & Compliance: MDR 2017 compliance; Electrical Safety certification; ISI/BIS-related certifications may be required depending on product category
  • Delivery & Training: installation, testing, commissioning, operator training, and statutory clearance support may be included
  • Vendor Status: OA/corporate status must meet government procurement eligibility; suppliers with registered Indian office for after-sales support preferred

Key Specifications

    • Product Name: Platelet Agitator and Incubator (V2)
    • Chamber Volume: not specified in extract; verify in BOM/spec sheet
    • Capacity: number of bags unspecified; confirm bag capacity in model spec
    • Alarms: presence of audible/visual alarms confirmed in spec
    • Shelves: number and dimensions to be confirmed (WDH)
    • Speed: RPM specification to be confirmed by model
    • Temperature Range: operating temperature window to be verified (°C)
    • Operating Range: environmental operating conditions to be confirmed
    • Printer: Thermal printer dimension in mm to be confirmed
    • Power: required power rating and phase type
    • Warranty: duration in years
    • Certifications: MDR 2017 compliance; Medical Device license; electrical safety; BIS/type test certificates

Terms & Conditions

  • Key Term 1: MDR 2017 compliance and valid Medical Device license required

  • Key Term 2: OEM/Authorized Seller with India-based after-sales support must be established

  • Key Term 3: Scope includes supply, installation, testing, commissioning, operator training, and statutory clearances

Important Clauses

Payment Terms

Payment terms not detailed in extract; bidders should anticipate standard government terms aligned with supply, installation, testing, and commissioning

Delivery Schedule

Delivery period not specified; option clause permits +/- 25% quantity variation and extended delivery time calculations

Penalties/Liquidated Damages

Penalties or LD provisions not explicitly stated; standard contract LD policies may apply for delays or non-conformance

Bidder Eligibility

  • 1 year minimum experience manufacturing/supplying similar platelet separator/incubator equipment to government entities

  • Not under liquidation, court receivership, or bankruptcy; undertake in bid

  • OEM authorization or proof of authorized reseller with India after-sales support

Additional Tender Data

Commercial Details

Tender Category

Goods

Bid To RA

No

Bid To RA Enabled

Yes

Item Category

Platelet Agitator and Incubator (V2) (Q2)

Authority Records

HEALTH AND FAMILY WELFARE SERVICES DEPARTMENT
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Documents 4

GeM-Bidding-9122544.pdf

Main Document

CATALOG-Specification-1

CATALOG Specification

Buyer uploaded ATC document

ATC

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 Name Platelet Agitator and Incubator
PRODUCT INFORMATION Material Stainless Steel
PRODUCT INFORMATION Chamber Volume (Ltr) 200
PRODUCT INFORMATION Capacity (Bag) 41 to 60
PRODUCT INFORMATION Alarms Available Low Temperature, High Temperature
PRODUCT INFORMATION Number of Shelves 3 to 6
PRODUCT INFORMATION Shelves Dimesion (W*D*H) 15*10*2
PRODUCT INFORMATION Speed (RPM) 50 to 10000
PRODUCT INFORMATION Temperature Range (Degree Celsius)) -80 to 24
PRODUCT INFORMATION Operating Range 10% of rated voltage
PRODUCT INFORMATION Printer (Thermal Printer) (mm) 30 mm
ELECTRICAL AND OPERATIONAL REQUIREMENT Power Requirement 200-240V,50Hz
ELECTRICAL AND OPERATIONAL REQUIREMENT Phase Type 3
WARRANTY Warranty in Years 5
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 Certification for manufacturing unit 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
CERTIFICATIONS Electrical Safety IEC 60601-1-2 or Equivalent BIS

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Required Documents

1

GST registration certificate

2

Permanent Account Number (PAN) card

3

Experience certificates for similar product supply

4

Financial statements (audited if available)

5

EMD/Security deposit documentation (as applicable)

6

Technical bid documents showing MDR compliance

7

BIS license type test certificates and approval certificates

8

OEM authorization/authorizations for resellers (if applicable)

9

Electrical Safety certification

10

Medical Device license issued under Drugs and Cosmetics Act

11

Test reports for each batch as per MDR 2017

Frequently Asked Questions

Key insights about PUDUCHERRY tender market

How to bid for the platelet incubator tender in Puducherry 2026?

Bidders must meet MDR 2017 compliance, possess a valid Medical Device license, and upload BIS/type test certificates along with OEM authorizations. Include proof of 1+ year government supply experience, GST, PAN, and financial statements. Submit installation, commissioning, and operator training plans with the bid.

What documents are required for the platelet incubator bid in Karikal?

Required documents include GST certificate, PAN, experience certificates for similar equipment, audited financial statements, OEM authorization, MDR compliance certificates, Medical Device license, BIS/type test certificates, and electrical safety certification. EMD submission, if applicable, must follow tender guidelines.

What standards and licenses must the supplier demonstrate for this medical device?

Suppliers must demonstrate MDR 2017 compliance, possession of a valid Medical Device license under the Drugs and Cosmetics Act, electrical safety certification, and BIS/type test certificates. OEM authorization for India-based after-sales support is also required for imported products.

What is the delivery scope for installation and training in this tender?

Scope includes supply, installation, testing, commissioning, operator training, and providing any required statutory clearances. Delivery timing will align with the contract, and the option clause allows a 25% quantity variation with adjusted delivery timelines.

What is the eligibility criteria for government procurement of platelet equipment?

Eligibility requires at least 1 year of regular supply of similar equipment to central/state government or PSU, no liquidation status, GST registration, and ability to provide OEM-based after-sales support in India. Demonstrated prior contracts with government entities strengthen eligibility.

What are the key certification requirements bidders must attach to the bid?

Attach MDR compliance confirmation, Medical Device license, Electrical Safety certificate, BIS license or type test certificates, and manufacturing unit certification. Ensure test reports per MDR 2017 are provided for each batch or product as required by the buyer.

When could the procurement lead to price variations or quantity adjustments?

The buyer reserves the right to increase/decrease quantity up to 25% at contract placement and during currency at contracted rates. Delivery time extensions are calculated as (increased quantity/original quantity) × original period, with a minimum of 30 days.

How to verify OEM after-sales support availability for this bid?

Verify that the OEM or authorized seller has a registered India office for after-sales service. Submit the related certificate proving Indian-based service capability, response times, and spare parts availability as part of the bid package.

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