Platelet Agitator and Incubator (V2)
N/a
PONDICHERRY, PUDUCHERRY
Bid Publish Date
14-Mar-2026, 4:45 pm
Bid End Date
25-Apr-2026, 6:00 pm
Location
Progress
Quantity
1
Bid Type
Two Packet Bid
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.
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
Payment terms not detailed in extract; bidders should anticipate standard government terms aligned with supply, installation, testing, and commissioning
Delivery period not specified; option clause permits +/- 25% quantity variation and extended delivery time calculations
Penalties or LD provisions not explicitly stated; standard contract LD policies may apply for delays or non-conformance
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
Tender Category
Goods
Bid To RA
No
Bid To RA Enabled
Yes
Item Category
Platelet Agitator and Incubator (V2) (Q2)
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Main Document
CATALOG Specification
ATC
GEM_GENERAL_TERMS_AND_CONDITIONS
N/a
PONDICHERRY, PUDUCHERRY
Indian Air Force
JORHAT, ASSAM
Central Health Service Ministry Of Health And Family Welfare
NEW DELHI, DELHI
Post Graduate Institute Of Medical Education And Research Chandigarh
SANGRUR, PUNJAB
Kamdhenu University
ANAND, GUJARAT
Tender Results
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| 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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GST registration certificate
Permanent Account Number (PAN) card
Experience certificates for similar product supply
Financial statements (audited if available)
EMD/Security deposit documentation (as applicable)
Technical bid documents showing MDR compliance
BIS license type test certificates and approval certificates
OEM authorization/authorizations for resellers (if applicable)
Electrical Safety certification
Medical Device license issued under Drugs and Cosmetics Act
Test reports for each batch as per MDR 2017
Key insights about PUDUCHERRY tender market
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.
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.
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.
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.
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.
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.
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.
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.
Commissionerate Of Food Safety
📍 ERNAKULAM, KERALA
Indian Council Of Agricultural Research (icar)
📍 RAIPUR, CHHATTISGARH
Northern Coalfields Limited
📍 SONBHADRA, UTTAR PRADESH
N/a
📍 KANCHIPURAM, TAMIL NADU
Indian Army
📍 MATHURA, UTTAR PRADESH
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Main Document
CATALOG Specification
ATC
GEM_GENERAL_TERMS_AND_CONDITIONS