Qualitative PCR Machine (Thermal Cycler)
National Institute Of Plant Genome Research
WEST DELHI, DELHI
Bid Publish Date
01-Jan-2026, 11:25 am
Bid End Date
05-Feb-2026, 5:00 pm
EMD
₹54,000
Location
Progress
Quantity
3
Bid Type
Two Packet Bid
The Department Of Atomic Energy invites bids for a Qualitative PCR Machine (Thermal Cycler) to be supplied, installed, tested and commissioned, with operator training and statutory clearances as required. The project requires an EMD of ₹54,000 and includes on-site installation, testing, commissioning, and operator training. The bidder must provide OEM authorization, ensure OEM-certified installation resources, and establish or demonstrate a functional service center in the state of the consignee. Compliance with Medical Device Rules (MDR 2017) and a valid Medical Device license are mandatory. The scope emphasizes end-to-end delivery, including statutory certifications, electrical safety, and batch testing reports. A potential on-site demonstration may be requested in the MMR region, with possible mobilization to ACTREC if needed. The procurement is framed to ensure turnkey delivery and post-delivery support from an OEM-authorized entity. The tender emphasizes adherence to mandatory certifications and post-sale service readiness to support safe deployment in the Atomic Energy Directorate context.
Qualitative PCR Machine (Thermal Cycler) with MDR 2017 compliance
Display type, USB ports, PC compatibility, and battery-backed UPS
Maximum Heating Ramp rate (°C/s) and Maximum Cooling Ramp rate (°C/s) specified; adjustable ramp rates
Operating temperature range and hot lid temperature clearly defined
Compatibility with well strips and individual PCR tubes
Input power supply and boot-up time specified
Batch test reports per MDR 2017; manufacturing unit certification
Electrical safety compliance and OEM authorization required
EMD ₹54,000 via DD to DIRECTOR, ACTREC; scan with bid and deliver hard copy within 5 days
OEM/OEM-certified installation required; distributor authorization if applicable
Service center in consignee state mandatory; establish within 30 days
Physical demonstration may be required in MMR region or ACTREC
EMD via DD; payment terms tied to delivery milestones and service center evidence; price elements to be in Financial Bid only
Supply, installation, testing, commissioning, and operator training; adherence to MDR-related certifications; demonstration if requested
Not explicitly stated; ensure compliance with delivery and installation milestones and post-delivery service expectations
OEM-authorized installation capability or OEM-certified resource
Functional service center in the state of consignee or commitment to establish within 30 days
Compliance with MDR 2017 and medical device licensing requirements
Main Document
CATALOG Specification
GEM_GENERAL_TERMS_AND_CONDITIONS
National Institute Of Plant Genome Research
WEST DELHI, DELHI
Forensic Science Laboratory
WEST TRIPURA, TRIPURA
Odisha Police
KHORDHA, ODISHA
Directorate Of Higher Education
SOUTH TRIPURA, TRIPURA
Indian Council Of Agricultural Research (icar)
NAINITAL, UTTARAKHAND
Tender Results
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| Category | Specification | Requirement |
|---|---|---|
| GENERAL INFORMATION | Product Description | Qualitative PCR Machine (Thermal Cycler) |
| PRODUCT INFORMATION | System Type | Open |
| PRODUCT INFORMATION | Display Type | LCD/LED |
| PRODUCT INFORMATION | Maximum Heating Ramp rate in degree per second (?C/s) | 5 |
| PRODUCT INFORMATION | Maximum Cooling Ramp rate in degree per second (?C/s) | 4 |
| PRODUCT INFORMATION | Adjustable Heating / Cooling Ramp Rate | Yes Or higher |
| PRODUCT INFORMATION | Operating Temperature range in Degree Celcius | 4 to 105 Degree Celcius |
| PRODUCT INFORMATION | Hot Lid Temperature | 30 to 110 Degree Celcius |
| PRODUCT INFORMATION | Compatibility for Well Strips | 8 well strips |
| PRODUCT INFORMATION | Compatibility for Individual PCR tubes | 0.1 to 0.2 ml tubes |
| PRODUCT INFORMATION | Input power supply | Single phase (230 V, 50 Hz) |
| PRODUCT INFORMATION | Compatible to be used with PC | Yes |
| PRODUCT INFORMATION | Availability of USB ports | 2 |
| PRODUCT INFORMATION | Battery backup of UPS (in hours) | NA if UPS not provided |
| PRODUCT INFORMATION | Boot up time | ≤1 minute |
| 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 Compliance | IEC 60601-1-2 or Equivalent BIS |
| WARRANTY | Warranty in Years (Option of comprehensive warranty is available through bidding only, which if opted will supersede normal warranty in the catalogue) | 2, 3, 4, 5 Or higher |
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PAN Card copy
GSTIN copy
Cancelled cheque
EFT mandate certified by bank
OEM authorization certificate (if bidding through authorized distributor)
Medical Device MDR 2017 compliance certificates
Medical Device license under Drugs and Cosmetic Act
Test reports for each batch as per MDR
Electrical safety compliance certificates
Proof of existing/established service center (or plan to establish within 30 days)
Extended Deadline
05-Feb-2026, 5:00 pm
Opening Date
05-Feb-2026, 5:30 pm
Extended Deadline
29-Jan-2026, 5:00 pm
Opening Date
29-Jan-2026, 5:30 pm
Key insights about MAHARASHTRA tender market
Bidders must submit all required documents, including PAN, GST, EFT mandate, and OEM authorization along with the EMD of ₹54,000 via DD to DIRECTOR, ACTREC. Compliance with MDR 2017 and a valid Medical Device license are mandatory. Demonstrations may be requested in MMR region and must be arranged by the bidder.
Required documents include PAN, GSTIN, cancelled cheque, EFT mandate, OEM authorization if applicable, MDR compliance certificates, Medical Device license, batch test reports, and evidence of a functional service center or plan to establish within 30 days.
The instrument must comply with MDR 2017, hold a valid Medical Device license under Drugs and Cosmetic Act, provide batch test reports per MDR, and demonstrate electrical safety compliance. Manufacturing unit certification is also required.
Post-bid opening, a physical demonstration may be requested at end-user site in MMR region or ACTREC. If the model is not installed nearby, the bidder may need to bring it to ACTREC within 10 days of the request.
EMD is ₹54,000, payable via Account Payee Demand Draft to DIRECTOR, ACTREC, KHARGHAR. Scanned DD proof must be uploaded with the bid; hard copy delivery to the buyer within 5 days after bid end/opening.
Bidder must have a functional service center in the consignment state or establish one within 30 days of award; payment release is contingent on submission of service capability evidence.
Scope includes supply, installation, testing, commissioning, and operator training; all statutory clearances needed, if any, and equipment handover with documentation as per buyer requirements.
A standard warranty is implied; optional comprehensive warranty can be elected during bidding, which would supersede the catalogue warranty. Ensure terms align with warranty coverage and service commitments.
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Main Document
CATALOG Specification
GEM_GENERAL_TERMS_AND_CONDITIONS