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Aspartate Amino Transferase test reagents/kit - India CDSCO Medical Device Registration

Aspartate Amino Transferase test reagents/kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2019/000034_5e9a0d4958dcfce6d084e9c288fe56b8_5cd1711f7da2cd0658bbeb48a2cae428. 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
Aspartate Amino Transferase test reagents/kit
UID: MFG/IVD/2019/000034_5e9a0d4958dcfce6d084e9c288fe56b8_5cd1711f7da2cd0658bbeb48a2cae428

Brand Name

GPO-PAP

Device Class

Class B

Approving Authority

Telangana

Product Information

Estimation of the enzyme Aspartate Amino Transferase (GPO-PAP) in serum/plasma

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