Ultrasound Combination Therapy Machine
Indian Air Force
AGRA, UTTAR PRADESH
Bid Publish Date
15-Jul-2026, 8:20 am
Bid End Date
27-Jul-2026, 10:00 am
Location
Progress
Quantity
1
Bid Type
Two Packet Bid
The Indian Air Force invites bids for an Ultrasound Combination Therapy Machine to be deployed in Chandigarh, CH 160001. The specification covers a dual-frequency ultrasound system with probes, BNR-compliant ultrasound probe, digital treatment timer display, waterproof design, headwarming on the applicator, and a flexible warranty option. Certification requirements include MDR 2017 compliance, valid licensing under the Drugs and Cosmetic Act 1940, and a certified manufacturing unit with batch test reports. The tender emphasizes submission of all certifications at bid or delivery, and supports quantity variation up to 25% during contract execution, with delivery timelines linked to the original delivery order. This opportunity targets suppliers capable of rigorous medical device compliance and reliable post-market support. Unique aspects include mandatory electrical compliance standards and the option to opt for comprehensive warranty superseding catalogue terms.
EMD amount and percentage: not specified; bidders must prepare as per buyer terms
Delivery flexibility: purchaser may increase/decrease quantity up to 25% during contract
Delivery period: calculated as (Additional quantity ÷ Original quantity) × Original delivery period, minimum 30 days
Certification requirements: MDR 2017 compliance, Medical Device license under Drugs and Cosmetic Act, manufacturing unit certification, batch test reports
Documentation: submit all certifications and test reports at bid submission or with supplies
Not specified in data; bidders should align with standard government payment practices and contract terms
Delivery must align with last-date-of-original-Delivery Order; option clause may extend delivery time; additional time formula included
Not detailed; ensure compliance with MDR timelines and delivery obligations to avoid LD
Experience in supplying medical devices (ultrasound or similar) to defense or government bodies
Valid Medical Device MDR 2017 compliance and Drugs and Cosmetics Act license
Manufacturing unit certification and batch test reporting capability
Tender Category
Goods
Bid To RA
No
Bid To RA Enabled
Yes
Item Category
Ultrasound Combination Therapy Machine (Q2)
Max Delivery Days
16
Delivery Locations
1
Delivery Cities
CHANDIGARH
| Consignee | Address | City | State | Pincode | Quantity | Delivery Days | Additional Requirement |
|---|---|---|---|---|---|---|---|
| - | CHANDIGARH | CHANDIGARH | - | - | 1 | 16 | - |
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Main Document
CATALOG Specification
ATC
GEM_GENERAL_TERMS_AND_CONDITIONS
Indian Air Force
AGRA, UTTAR PRADESH
Indian Air Force
NAGPUR, MAHARASHTRA
Health Services
AIZAWL, MIZORAM
Dr. Ram Manohar Lohia Institute Of Medical Sciences
LUCKNOW, UTTAR PRADESH
Dr. Ram Manohar Lohia Institute Of Medical Sciences
LUCKNOW, UTTAR PRADESH
Tender Results
Loading results...
| Category | Specification | Requirement |
|---|---|---|
| GENERAL INFORMATION | Product Description | Ultrasound Combination Therapy Machine |
| PRODUCT INFORMATION | Number of channels of electrotherapy unit provided | 2 |
| PRODUCT INFORMATION | Number of electrodes provided | 4 |
| PRODUCT INFORMATION | Dual frequency ultrasound with probes provided | 1 MHz and 3 Mhz |
| PRODUCT INFORMATION | Perform parameters | IFT, TENS, Russian, Galvanic, Monophasis, Variable muscle stimulation, Diadynamic, High voltage pulse current, Microcurrent, Surged/Faradic |
| PRODUCT INFORMATION | Body diagram with associated clinical programs | Yes |
| PRODUCT INFORMATION | Ultrasound probe should have BNR to prevent hotspots | less than 5.0 (BNR) |
| PRODUCT INFORMATION | Digital display of treatment time | Yes |
| PRODUCT INFORMATION | Power supply (V) | 100 to 240V, 50 Hz |
| PRODUCT INFORMATION | Waterproof | Yes |
| PRODUCT INFORMATION | Headwarming on ultrasound applicator | Yes, No |
| 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 Compliance Standard | IEC 60601 or BIS Equivalent |
| WARRANTY | 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 |
Discover companies most likely to bid on this tender
GST certificate
PAN card
Experience certificates (similar medical device deployments)
Financial statements (last financial year and audited if available)
EMD/Security deposit documentation
Technical bid documents (compliance matrix, technical specs)
OEM authorization / manufacturing license
Medical Device MDR 2017 certificates and batch test reports
Electrical compliance certificates
Drugs and Cosmetics Act license or copy of license
Key insights about CHANDIGARH tender market
Bidders must submit MDR 2017 compliance certificates, Medical Device license under Drugs and Cosmetic Act, batch test reports, and OEM authorization along with technical bid. Ensure power specifications, waterproofing, BNR probe compliance, and dual-frequency capability are clearly demonstrated in the technical offer.
Required documents include GST registration, PAN card, audited financial statements, experience certificates for similar devices, EMD documentation, OEM authorizations, medical device certifications, and electrical compliance certificates. Prepare batch test reports for MDR 2017 and license copies for submission.
The device must comply with MDR 2017, possess a valid Medical Device license under Drugs and Cosmetic Act 1940, have manufacturing unit certification, and provide MDR-compliant batch test reports. Electrical compliance certificates are also required for bid submission.
The buyer may increase or decrease quantity up to 25% of the bid quantity at contract placement and during the currency of contract, with delivery time calculated as specified by the option clause and minimum 30 days, starting from the last date of the original delivery order.
A comprehensive warranty option is available during bidding, which, if chosen, will supersede the standard catalogue warranty. Confirm scope of coverage and duration in the bid response and ensure post-warranty service terms are defined.
Bidders must provide OEM authorizations, proof of manufacturing unit certification, and batch test reports per MDR 2017. Ensure the supplier can deliver medical device licenses and electrical compliance certificates with the bid and along with supplies.
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Pimpri Chinchwad Municipal Corporation
📍 PUNE, MAHARASHTRA
Indian Air Force
All India Institute Of Medical Sciences (aiims)
📍 NADIA, WEST BENGAL
Jawaharlal Institute Of Postgraduate Medical Education And Research (jipmer)
📍 EAST GODAVARI, ANDHRA PRADESH
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Main Document
CATALOG Specification
ATC
GEM_GENERAL_TERMS_AND_CONDITIONS