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Creatine Kinase-MB Assay Kit - India CDSCO Medical Device Registration

Creatine Kinase-MB Assay Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2022/000139_7bee2f3f9371e6d182fb3c0af62ae8ee_9729573eaffca74a3fb5ccd5193882fa. This device is marketed under the brand name TG. The license holder is ADcare Bio Medicals,, 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
Creatine Kinase-MB Assay Kit
UID: IMP/IVD/2022/000139_7bee2f3f9371e6d182fb3c0af62ae8ee_9729573eaffca74a3fb5ccd5193882fa

Brand Name

TG

License Holder

ADcare Bio Medicals,

Device Class

Class B

Approving Authority

CDSCO

Product Information

It is used for in vitro quantitative determination of creatine kinase -MB (TG) in human serum or plasma

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