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FT3 Assay (FT3 Assay ) - India CDSCO Medical Device Registration

FT3 Assay (FT3 Assay ) is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2023/000207_dd1e173c7d460759a869c1fe8a9767d8_24b907773136f23d8408552ccddfd3df. 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
FT3 Assay (FT3 Assay )
UID: IMP/IVD/2023/000207_dd1e173c7d460759a869c1fe8a9767d8_24b907773136f23d8408552ccddfd3df

Brand Name

CLIA

License Holder

Rapid House

Device Class

Class B

Approving Authority

CDSCO

Product Information

FT3 Assay (CLIA) is for the in vitro quantitative determination of free triiodothyronine (CLIA) in human serum and plasma

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