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Employees State Insurance Corporation Intermittent Pneumatic Compression Device Tender Tirunelveli Tamil Nadu MDR 2017 2026

Bid Publish Date

16-May-2026, 9:53 am

Bid End Date

06-Jun-2026, 10:00 am

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Progress

Issue16-May-2026, 9:53 am
Corrigendum01-Jun-2026
AwardPending
Explore all 4 tabs to view complete tender details

Quantity

2

Bid Type

Two Packet Bid

Key Highlights

  • Brand/OEM requirements: explicit OEM authorizations and in-state service centers
  • Technical certifications: MDR 2017 compliance, Medical Device Rules, Electrical Safety Standard
  • Special clauses: 25% quantity variation, 30-day service center setup if absent
  • Eligibility criteria: in-state service presence, installation/commissioning capability, training provision
  • Warranty/AMC: comprehensive warranty option available via bidding
  • Penalties/Performance: LDs and alternative arrangements for non-performance

Categories 1

Tender Overview

Employees State Insurance Corporation seeks procurement of an Intermittent Pneumatic Compression Device (V2) – Q2 for delivery to Tirunelveli, Tamil Nadu. The tender covers a comprehensive device suite including controller, inflatable garments, and accessories with required installation, user training, and safety checks. Key differentiators include advanced venous refill detection, USB software updates, dual-leg display, alarms for leaks and overpressure, and optional comprehensive warranty. The contract implies on-site support, service centers in-state, and adherence to MDR 2017 and Drugs and Cosmetic Act licenses. Expected scope emphasizes hospital-grade cleaning compatibility, ergonomic design, and single/both-leg operation capability.

Technical Specifications & Requirements

  • Compression with venous refill detection technology for limb therapy
  • Pressure adjustable range and precise control via cuff knobs
  • Approx cycle time / inflation / deflation times in seconds; controller displays for each leg
  • Graphical user interface size on controller with touch screen display and screen type details
  • Separate pressure display for each leg and indication of inflated leg
  • Controller materials compatible with hospital-grade cleaners; USB port for software updates
  • Alarms for leaks and max pressure, automatic shutdown at max limit, and troubleshooting index
  • Ergonomic handle with bed mount, built-in cord storage, and single/both-leg operation option
  • Battery-backed power supply with specified battery type and runtime
  • Required certifications: MDR 2017 compliance, valid drug license, manufacturing unit certification, MDR-related test reports, electrical safety standards, and submission of all licenses/test reports at bid or delivery
  • Installation, safety checks, and user training by supplier; OEM authorizations and service centers in-state
  • Warranty options including optional comprehensive warranty via bidding; service support details (dedicated toll-free number) and on-site warranty terms

Terms, Conditions & Eligibility

  • Option to increase/decrease quantity by up to 25% at contract placement and during currency with extended delivery calculations
  • Provide dedicated toll-free service support and ensure an in-state service center presence; establish a center within 30 days if not existing
  • Submission requirements include all MDR certifications, drug licenses under the Drugs and Cosmetic Act, test reports, and manufacturing certifications
  • Assignment restrictions: no subletting without written consent of Medical Superintendent, ESIC Hospital, Tirunelveli; supplier responsible for installation, testing, and commissioning
  • Payment terms, delivery schedules, and penalties to align with buyer terms; warranty/AMC options governed by tender terms
  • Ensure brand/new equipment; strict adherence to installation and training clauses; readiness for on-site safety checks and operation handover

Key Specifications

  • Intermittent Pneumatic Compression Device with Venous refill detection

  • Pressure adjustable range and cuff pressure control

  • Dual-leg independent pressure display

  • Graphical touchscreen controller with USB software update port

  • Automatic overpressure shutdown and audible/visual alarms

  • Single/both-leg operation with ergonomic housing and bed mount

  • Integrated battery backup with specified runtime

  • MDR 2017 compliance, drug license under Drugs and Cosmetic Act, electrical safety standard

Terms & Conditions

  • Quantity flexibility up to 25% with adjusted delivery period

  • In-state service center requirement and toll-free service support

  • Mandatory installation, safety checks, and user training by supplier

Important Clauses

Payment Terms

Details to be as per buyer terms; payment release after delivery milestones and service acceptance per ESIC

Delivery Schedule

Delivery period linked to last date of original delivery order; extended time calculations apply with defined minimums

Penalties/Liquidated Damages

Penalties/LDs likely for delayed delivery or non-compliance; breach leads to potential alternative arrangements at supplier risk

Bidder Eligibility

  • In-state service center presence or ability to establish within 30 days of award

  • Experience in supplying medical devices with MDR compliance

  • OEM authorization and capability for installation, testing, and training

Additional Tender Data

Commercial Details

Tender Category

Goods

Bid To RA

No

Bid To RA Enabled

Yes

Item Category

Intermittent Pneumatic Compression Device (V2) (Q2)

Authority Records

MINISTRY OF LABOUR AND EMPLOYMENT
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Documents 4

GeM-Bidding-9308091.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
PRODUCT TECHNICAL SPECIFICATIONS Compression Sequential, Gradient and circumferential pneumatic compression around the ankle, calf and then the thigh
PRODUCT TECHNICAL SPECIFICATIONS Venous refill detection technology Yes
PRODUCT TECHNICAL SPECIFICATIONS Pressure Adjustable Range 40 to 65 mmHg, 25 to 120 mmHg, 30 to 130 mmHg, 20 to 160 mmHg, Upto 180 mmHg, Upto 200 mmHg, Upto 280 mmHg Or higher
PRODUCT TECHNICAL SPECIFICATIONS Approx Cycle Time (seconds) 60.0
PRODUCT TECHNICAL SPECIFICATIONS Approx Inflation time (seconds) 10 to 15 seconds
PRODUCT TECHNICAL SPECIFICATIONS Approx Deflation time (seconds) 45 to 50 seconds
PRODUCT TECHNICAL SPECIFICATIONS Graphical user interface size in the controller unit ≥ 3.2 inch
PRODUCT TECHNICAL SPECIFICATIONS Touch Screen Display Yes
PRODUCT TECHNICAL SPECIFICATIONS Type of Screen LED Or higher
PRODUCT TECHNICAL SPECIFICATIONS Separate pressure display of both legs & indicating the Inflated Leg Yes
PRODUCT TECHNICAL SPECIFICATIONS Material of controller unit should be compatible with most of hospital grade cleaning agents Yes
PRODUCT TECHNICAL SPECIFICATIONS USB port in controller to make software updates easy Yes
PRODUCT TECHNICAL SPECIFICATIONS Knobs for each cuff for setting and adjusting the pressure Yes
PRODUCT TECHNICAL SPECIFICATIONS Provision of preset audible and visual alarms for leaks and maximum pressure Yes
PRODUCT TECHNICAL SPECIFICATIONS Facility of automatic shutdown if pressure exceeds the maximum limit Yes
PRODUCT TECHNICAL SPECIFICATIONS Facility of trouble shooting index in the device itself Yes
PRODUCT TECHNICAL SPECIFICATIONS Ergonomic Handle and integrated bed mount with built in power cord storage Yes
PRODUCT TECHNICAL SPECIFICATIONS Option of single leg usage or both if needed Yes
PRODUCT TECHNICAL SPECIFICATIONS Locking feature that prevents accidental or intentional changing or prescribed settings Yes
PRODUCT TECHNICAL SPECIFICATIONS Item weight (Kg) ≤ 5 kg
GENERAL FEATURES Product Description Intermittent Pneumatic Compression Device
GENERAL FEATURES Controller unit Portable, lightweight with handle
ACCESSORIES Type of Inflatable garment/sleeve provided Knee length, Thigh length, Foot cuff
ACCESSORIES Usage of inflatable garment/sleeve Disposable, Reusable
ACCESSORIES Size of sleeves/cuff provided S, M, L, XL, XXL
ACCESSORIES Number of Disposable garments/sleeves Provided 10, 20, 30, 50, 100 Or higher
ACCESSORIES Number of Reusable garments/sleeves Provided 2
ELECTRICAL FEATURES Integrated Battery for power backup for uninterrupted compression Yes
ELECTRICAL FEATURES Type of battery Li-ion, Li-Polymer
ELECTRICAL FEATURES Battery backup time (Hrs) 4, 5 Or higher
CERTIFICATIONS & REPORTS Compliance to Medical Device Rules (MDR) 2017 as amended till date Yes
CERTIFICATIONS & REPORTS Availability of valid drug 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 & REPORTS Manufacturing unit certification ISO:13485 (Latest)
CERTIFICATIONS & REPORTS Availability of Test Report for product as per Medical Device Rules (MDR) 2017 as amended till date Yes
CERTIFICATIONS & REPORTS Compliance to Electrical Safety Standard IEC 60601-1 or Equivalent BIS Standrad
CERTIFICATIONS & REPORTS Submission of all necessary certifications, licenses and test reports to the buyer at the time of bid submission and/or along with supplies as per buyer requirement Yes
INSTALLATION & TRAINING Supplier to perform installation, safety and operation checks before handover Yes
INSTALLATION & TRAINING Training of users in operation and basic maintenance shall be provided Yes
WARRANTY & MAINTENANCE Warranty in Years (Option of comprehensive warranty is available through bidding only, which if opted will supersede normal warranty in the catalogue) 5 Or higher

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Required Documents

1

GST registration certificate

2

PAN card

3

Experience certificates for comparable medical device supply

4

Financial statements (audited or management accounts)

5

EMD/Security deposit documentation (as applicable)

6

Technical bid documents confirming MDR compliance and device specs

7

OEM authorization and service center proof in-state

Corrigendum Updates

1 Update
#1

Update

01-Jun-2026

Extended Deadline

06-Jun-2026, 10:00 am

Opening Date

06-Jun-2026, 10:30 am

Frequently Asked Questions

Key insights about TAMIL NADU tender market

How to bid for ESIC Tirunelveli pneumatic compression tender in 2026

Bidders must meet in-state service center eligibility, MDR compliance, and provide OEM authorizations. Submit technical and financial bids with MDR 2017 certificates, drug license, and electrical safety compliance. Include installation, training plan, and dedicated service support details. Follow ESIC terms for quantity variation up to 25% and delivery schedules.

What documents are required for ESIC compression device tender in Tamil Nadu

Submit GST and PAN, financial statements, experience certificates for similar medical devices, MDR compliance documents, drug license under Drugs and Cosmetic Act, manufacturing unit certification, test reports, OEM authorization, and proof of in-state service center.

What are the technical specifications for the ESIC device in this bid

Device must support venous refill detection, adjustable cuff pressure, dual-leg separate display, graphical touchscreen controller, USB port for software updates, audible/visual alarms, automatic overpressure shutdown, and battery backup with specified runtime; device weight and sleeve sizes as per catalog.

When is delivery expected for ESIC Tirunelveli pneumatic device order

Delivery window ties to original order date; option to increase quantity up to 25% with extended delivery period calculated as (increased quantity/original quantity) × original days, minimum 30 days; service installation occurs before handover.

What are the warranty and service terms for this ESIC bid

Warranty options include standard terms plus the possibility of a comprehensive warranty via bidding; service centers must be functional in-state; toll-free support must be provided; penalties apply for non-performance or delayed service.

What certifications must accompany the bid for MDR compliance

Bids must include MDR 2017 compliance evidence, Drug License under Act 1940, Electrical Safety Standard compliance, Manufacturing Unit Certification, and test reports; provide copies at bid submission and with supplies as required by ESIC.

What is required for installation and user training under ESIC terms

Supplier must perform on-site installation, safety and operation checks, and deliver user training on operation and basic maintenance; training plan, manuals, and handover checklist should be included with the bid and delivered during handover.

How does quantity variation affect delivery under this tender

The purchaser may adjust quantity by up to 25% at contract award and during contract currency; delivery period recalculations apply, ensuring minimum 30 days extension as specified; ensure ability to scale supply accordingly.

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