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T3 Rapid Quantitative Test - India CDSCO Medical Device Registration

T3 Rapid Quantitative Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2019/000039_9ffb1efd4bb20a81eae068b15a52a916_6e511b6a2630649a8264a9b51624996c. This device is marketed under the brand name Finecare . The license holder is M/s Avantor Performance Materials India Ltd, and it is classified as Device Class Class B. The approving authority is CDSCO.

This page provides comprehensive regulatory information including complete registration details, license holder information, device classification, and related products. Pure Global AI offers free access to 71,807+ India medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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CDSCO Registered
Class Class B
T3 Rapid Quantitative Test
UID: IMP/IVD/2019/000039_9ffb1efd4bb20a81eae068b15a52a916_6e511b6a2630649a8264a9b51624996c

Brand Name

Finecare

Device Class

Class B

Approving Authority

CDSCO

Product Information

Quantitative determination of Triiodothyronine (Finecare ) in human serum, plasma or whole blood. The test is used as an aid to the assessment of thyroid function

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