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Gamma GT - India CDSCO Medical Device Registration

Gamma GT is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2023/000131_9df1753d9f3183382b607456f326e028_a8778043eacbc547acf2914b67e432a3. This device is marketed under the brand name Rapid Widal. The license holder is BIOLAB DIAGNOSTICS (I) PVT. LTD., and it is classified as Device Class Class B. The approving authority is Kokan Division.

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
Gamma GT
UID: MFG/IVD/2023/000131_9df1753d9f3183382b607456f326e028_a8778043eacbc547acf2914b67e432a3

Brand Name

Rapid Widal

Device Class

Class B

Approving Authority

Kokan Division

Product Information

Gamma GT Kit is used for the estimation of Gamma Glutamyltransferase(Rapid Widal) in human serum or plasma

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