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Government Tender Published for Dual Frequency Ultrasound Therapy Unit (V2) in CUDDALORE, TAMIL NADU

Bid Publish Date

16-May-2026, 11:40 am

Bid End Date

09-Jun-2026, 3:00 pm

Generate Docs

Progress

Issue16-May-2026, 11:40 am
Corrigendum06-Jun-2026
AwardPending
Explore all 4 tabs to view complete tender details

Quantity

2

Bid Type

Two Packet Bid

Categories 3

A tender has been published for Nlc India Limited Dual Frequency Ultrasound Therapy Unit (V2) (Q2) in CUDDALORE, TAMIL NADU. Quantity: 2 by. Submission Deadline: 09-06-2026 15: 00: 00. Check eligibility and apply.

Additional Tender Data

Commercial Details

Tender Category

Goods

Bid To RA

No

Bid To RA Enabled

No

Item Category

Dual Frequency Ultrasound Therapy Unit (V2) (Q2)

Authority Records

MINISTRY OF COAL
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Documents 5

GeM-Bidding-9279348.pdf

Main Document

CATALOG-Specification-1

CATALOG Specification

Other Documents

OTHER

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 Product Description Dual Frequency Ultrasound Therapy Unit
PRODUCT INFORMATION Dual frequency Ultrasound Frequency 1 MHz - 3 MHZ
PRODUCT INFORMATION Touch panel screen Yes
PRODUCT INFORMATION Display Type LCD/LED/TFT
PRODUCT INFORMATION Display Size Atleast 7 inch
PRODUCT INFORMATION Beam non-uniformity ratio (BNR) should be less than 4 to prevent hotspots and tissue damage Yes
PRODUCT INFORMATION Modes Continuous & Pulsed
PRODUCT INFORMATION Duty cycle 5,10,20,30,40,50 and 100%
PRODUCT INFORMATION Pre-programmed protocols More than 40
PRODUCT INFORMATION Ultrasound power density,(Watts/cm2) 2 to 3
PRODUCT INFORMATION Treatment Time, adjustable (min) Atleast upto 30 min
PRODUCT INFORMATION Alarms Audio Alarm at the end of treatment with auto cutoff
PRODUCT INFORMATION Power supply 220 - 240V, 50Hz
PRODUCT INFORMATION Waterproof lightweight probe Yes
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 Conformity for electrical safety standard IEC-60601 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) 3.0

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Required Documents

1

Certificate (Requested in ATC) *In case any bidder is seeking exemption from Experience / Turnover Criteria

2

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

Corrigendum Updates

1 Update
#1

Update

06-Jun-2026

Extended Deadline

09-Jun-2026, 3:00 pm

Opening Date

09-Jun-2026, 3:30 pm

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