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Creatine Kinase test reagents/kit - India CDSCO Medical Device Registration

Creatine Kinase test reagents/kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2019/000034_dd8afe64d0373dcfd48ed91deae98763_fe85ea06786b2e3db25fba9c2970336b. 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
Creatine Kinase test reagents/kit
UID: MFG/IVD/2019/000034_dd8afe64d0373dcfd48ed91deae98763_fe85ea06786b2e3db25fba9c2970336b

Brand Name

GPO-PAP

Device Class

Class B

Approving Authority

Telangana

Product Information

To estimate the enzyme creatine phosphokinase or its isoenzymes in serum/plasma

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