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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_0bda008c5f88bcbbbfa59b865b0a2ec6. 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_0bda008c5f88bcbbbfa59b865b0a2ec6

Brand Name

CLIA

License Holder

Rapid House

Device Class

Class B

Approving Authority

CDSCO

Product Information

T3 Assay (CLIA) is for the in vitro quantitative determination of triiodothyronine (CLIA) in human serum and plasma

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