GEM

NIMHANS Blood Fluid Warming Cabinet Tender Bangalore Karnataka 81-105 L IS 13485 MDR 2017 2026

Bid Publish Date

05-Jan-2026, 3:37 pm

Bid End Date

27-Jan-2026, 11:00 am

Progress

Issue05-Jan-2026, 3:37 pm
AwardPending
Explore all 4 tabs to view complete tender details

Quantity

2

Bid Type

Two Packet Bid

Key Highlights

  • Brand/OEM and certification focus: ISO 13485
  • Technical standards required: MDR 2017 compliance, IEC 60601-1-2 safety, BIS equivalent
  • Special conditions: Price validity 1 year; external Po for extra quantities outside GeM
  • Critical eligibility: Govt/PSU supply experience with supporting PO or PO copy
  • Warranty/AMC expectations: explicit warranty clauses to be provided; training included
  • Penalties/SD: No explicit LDs listed; ensure clear penalties policy in bid
  • Delivery/installation: Includes ISTC and operator training; may require statutory clearances
  • Documentation to submit: MDR test reports, medical device licenses, GST, PAN, OEM authorizations

Categories 3

Tender Overview

The National Institute Of Mental Health And Neurosciences (NIMHANS), Department Of Health And Family Welfare, invites bids for a Blood Fluid Warming Cabinet. The device supports warming blood and IV fluids, with an 81-105 L capacity, PID temperature control, and a large LED display. Compliance targets include MDR 2017, valid Medical Device License, ISO 13485 certification, and batch-wise test reports. The unit features stainless steel interior, powder-coated exterior, and adjustable heated air circulation to ensure uniform chamber temperature. Electrical safety adheres to IEC 60601-1-2 or BIS equivalents. Delivery, installation, testing, commissioning, operator training, and statutory clearances are bundled in the scope. Quoted price must remain valid for one year. The L1 vendor may be awarded PO outside the GeM portal for additional quantities.

Key differentiators include PID-based control with PT100 sensing, 0.1°C resolution, and MDR/Medical Device licensing compliance. The tender targets suppliers capable of providing comprehensive after-sales support and documentation at bid submission.

Technical Specifications & Requirements

  • Product category: Blood Fluid Warming Cabinet
  • Capacity range: 81 to 105 liters
  • Temperature range: +25 to 80°C with uniform distribution via heated air circulation
  • Control system: PID controller with PT100 sensor and LED display
  • Materials: Interior stainless steel 304; exterior powder-coated GI
  • Safety: Integrated voltage protection; alarms for temperature failure
  • Standards & compliance: MDR 2017; IS 13485 certified manufacturer; IEC 60601-1-2 / BIS safety; Medical Device License under Drugs & Cosmetic Act
  • Documentation/Testing: Batch-wise test reports per MDR; proof of licenses and certifications at bid submission or delivery
  • Warranty & support: Warranty terms specified in bid; training of operators included
  • BoQ/quantities: No BOQ items listed; scope includes supply, installation, testing, commissioning, and operator training
  • Delivery scope: Includes statutory clearances if any; quotation valid for one year

Terms, Conditions & Eligibility

  • EMD: Not explicitly stated in data; bidders to reference EMD submission per T&C and RTGS/online transfer options via The Director, NIMHANS
  • Experience: Experience certificate for supply to Govt/PSU/renowned private org required with supply/purchase order
  • Delivery/Installation: Supply, installation, testing, commissioning, operator training; includes statutory clearances
  • Payment: Online RTGS/IBAN options; format requires bid ref and bidder name in transfer details; PO payment terms unspecified beyond supply scope
  • Documents: GST, PAN, experience certificates, financial statements, EMD proof, OEM authorizations, medical device licenses, MDR/test reports
  • Warranty/Penalty: Warranty details to be provided; penalties not specified in available data; ensure compliance with MDR and ISO 13485
  • Special Clause: Price validity of one year; L1 firm may receive additional orders outside GeM
  • Brand/OEM: ISO 13485 and MDR-compliant manufacturing units preferred; OEM authorizations recommended

Key Specifications

  • Blood Fluid Warming Cabinet with 81-105 L capacity

  • Temperature range +25 to 80°C with 0.1°C resolution; PID control via PT100

  • Interior: Stainless steel 304; Exterior: powder-coated GI

  • LED display and alarms for temperature failure; integrated voltage protection

  • MDR 2017 compliance; ISO 13485 certified manufacturer; valid Medical Device License

  • Batch-wise test reports per MDR 2017; IEC 60601-1-2 safety standard

Terms & Conditions

  • Bid price valid for 1 year; L1 may receive extra PO outside GeM

  • EMD/PMF as per T&C; RTGS/online payment allowed with proof

  • Supply, installation, testing, commissioning, training, and statutory clearances included

Important Clauses

Payment Terms

Online RTGS/IBN transfer accepted; bidders must include transfer details and upload proof with bid; no fixed advance term specified

Delivery Schedule

Scope includes supply, installation, testing, commissioning and operator training; delivery timeline to be defined in PO

Penalties/Liquidated Damages

No explicit LD details provided in data; bidders should seek clarity on penalties in final bid document

Bidder Eligibility

  • Experience certificate for supply of similar medical devices to Govt/PSUs or renowned private organizations

  • MSME/NSIC exemption certificates if applicable

  • Evidence of MDR/ISO 13485 compliance and medical device license

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Technical Specifications 1 Item

Item #1 Details

View Catalog
Category Specification Requirement
PRODUCT INFORMATION Capacity in Liters 5 to 30, 31 to 55, 56 to 80, 81 to 105, 106 to 130, 131 to 155, 156 to 180, 181 to 205, 206 to 230, 231 to 255, 256 to 280, 281 to 305
WARRANTY Warranty 1, 2, 3, 4, 5

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Required Documents

1

GST registration certificate

2

Permanent Account Number (PAN) card

3

Experience certificates for supply to Govt/PSU/private sector with PO copies

4

Financial statements (last 3 years) demonstrating financial capacity

5

EMD submission proof or MSME/NSIC exemption certificate (if applicable)

6

Technical compliance certificates for MDR and ISO 13485

7

OEM authorization from manufacturer (if distributor)

8

Medical Device License number and MDR batch test reports

9

Delivery, installation, testing, commissioning plan

10

Training proposal for operators

Frequently Asked Questions

Key insights about KARNATAKA tender market

How to bid for the blood fluid warming cabinet tender in Bengaluru?

Bidders must submit GST, PAN, experience certificates, financial statements, MDR/test reports, OEM authorizations, and EMD proof. The tender requires ISO 13485 and MDR compliance, plus a detailed delivery/installation and training plan. Include online payment receipt and bid reference in transfer details.

What documents are required for NIMHANS blood warming cabinet bid in Karnataka?

Required documents include GST certificate, PAN card, 3-year financials, MDR test reports, ISO 13485 certificate, Medical Device License details, OEM authorization (if applicable), and previous Govt/PSU supply PO copies. Also include installation and commissioning plan with training details.

What are the technical standards for the warming cabinet in this bid?

Device must comply with MDR 2017, ISO 13485 for the manufacturer, IEC 60601-1-2 safety standard, BIS equivalents, and valid Medical Device License under Drugs & Cosmetic Act. Batch test reports must be provided for each product lot.

What is the capacity and temperature range for the cabinet in this tender?

The cabinet must offer a capacity of 81-105 liters with a temperature range of +25 to 80°C and 0.1°C temperature resolution using a PID controller and PT100 sensor for accurate control.

When is the price validity for the NIMHANS tender in Bengaluru 2026?

Quoted price must be valid for one year from the bid submission date; additional quantities may be placed outside GeM with the L1 firm referenced in the tender terms.

What are the delivery and installation expectations for this bid?

Scope includes supply, installation, testing, commissioning, operator training, and any required statutory clearances. The supplier must provide a complete handover package and training plan for hospital staff.

What is required for warranty and after-sales support in this tender?

Warranty terms must be specified in the bid; manufacturer ISO 13485 compliance and MDR certifications are essential. After-sales support details, service response times, and availability of spare parts should be included.

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