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Tender Notice for ECG Electrodes (V2) in SOUTH DELHI, DELHI

Bid Publish Date

22-Jun-2026, 5:05 pm

Bid End Date

13-Jul-2026, 5:00 pm

EMD

₹60,000

Progress

Issue22-Jun-2026, 5:05 pm
AwardPending
Explore all 4 tabs to view complete tender details

Quantity

1000000

Bid Type

Two Packet Bid

Categories 1

All India Institute Of Medical Sciences (aiims) has released a public tender for ECG Electrodes (V2) (Q2) in SOUTH DELHI, DELHI. Quantity: 1000000. Submission Deadline: 13-07-2026 17: 00: 00. Download documents and apply online.

Additional Tender Data

Commercial Details

Tender Category

Goods

Bid To RA

No

Bid To RA Enabled

Yes

Item Category

ECG Electrodes (V2) (Q2)

Authority Records

MINISTRY OF HEALTH AND FAMILY WELFAREHEALTH AND FAMILY WELFARE DEPARTMENT

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Bid Preparation GeM Registration Document Filing

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Documents 4

GeM-Bidding-9504394.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 Features Product Description ECG Electrodes
Product Information Usage Adult, Pediatric
Product Information Shape Oval, Round, Tear Drop
Product Information Disposable Yes
Product Information MRI Compatible No, Yes
Product Information X-ray Translucence Yes
Product Information Integrated Abrader No, Yes
Dimensions Electrode Size (in mm x mm) 31.75 X 31.75, 35 X 30, 52 X 35
Dimensions Integrated Lead Wire Provided No
Material & Characteristics Substrate Material Polyethylene Foam
Material & Characteristics Gentle Adhesion Without Risk of Skin Trauma Yes
Material & Characteristics Non-irritant, Non-Allergic Gel Type Solid
Material & Characteristics Sensor Polymer Ag/AgCl plated ABS
Certifications Compliance to Medical Device Rule (MDR) 2017 as amended till date Yes
Certifications 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 Manufacturing unit certification 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 Standards IEC/EN 60601-1 or equivalent BIS Standard
Shelf Life Shelf life in months from the date of manufacture 36.0, 24.0
Shelf Life Minimum shelf life of the product at the time of delivery to the consignee 3/4 th of Total Shelf Life

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Historical Data

Required Documents

1

Experience Criteria

2

Past Performance

3

Certificate (Requested in ATC)

4

OEM Authorization Certificate

5

Additional Doc 1 (Requested in ATC)

6

Compliance of BoQ specification and supporting document *In case any bidder is seeking exemption from Experience / Turnover Criteria

7

the supporting documents to prove his eligibility for exemption must be uploaded for evaluation by the buyer

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