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Gamma test reagent/kit - India CDSCO Medical Device Registration

Gamma test reagent/kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2019/000034_4c2f72acb0d44d88dfc6842628f53d8a_866daa6bef3cca94de93fd335b010a50. This device is marketed under the brand name GPO-PAP. The license holder is ADI Diagnostics Pvt Ltd, and it is classified as Device Class Class B. The approving authority is Telangana.

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 test reagent/kit
UID: MFG/IVD/2019/000034_4c2f72acb0d44d88dfc6842628f53d8a_866daa6bef3cca94de93fd335b010a50

Brand Name

GPO-PAP

Device Class

Class B

Approving Authority

Telangana

Product Information

Estimation of the enzyme Gamma Glutamyl Transferase (GPO-PAP) in serum / plasma

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