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T3 Assay (T3 Assay ) - India CDSCO Medical Device Registration

T3 Assay (T3 Assay ) is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2023/000207_afe962565ddbaff0f6783b472407322e_a3740202be058034daa7a3c7a3982c3e. This device is marketed under the brand name CLIA. The license holder is Rapid House, 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 Assay (T3 Assay )
UID: IMP/IVD/2023/000207_afe962565ddbaff0f6783b472407322e_a3740202be058034daa7a3c7a3982c3e

Brand Name

CLIA

License Holder

Rapid House

Device Class

Class B

Approving Authority

CDSCO

Product Information

The kit is used for the quantitative in vitro detection of triiodothyronine in human serum, plasma or whole blood samples

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