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FA - India CDSCO Medical Device Registration

FA is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2022/000356_c3d3b557f996e0fc0f4c9147cb931fb1_858fadb6751da7196901b035ced179fe. This device is marketed under the brand name CLIA. The license holder is Diatek Healthcare Private Limited, 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
FA
UID: IMP/IVD/2022/000356_c3d3b557f996e0fc0f4c9147cb931fb1_858fadb6751da7196901b035ced179fe

Brand Name

CLIA

Device Class

Class B

Approving Authority

CDSCO

Product Information

FA (CLIA) test kit is a medical device intended for the estimation of FA in human serum

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