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CK-MB - India CDSCO Medical Device Registration

CK-MB is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2018/000023_8a863ab9781ae23a57fffc35f97a621d_297d816ab4539b867ee7bb8e92de8832. This device is marketed under the brand name AUTOPAK™. The license holder is Siemens Healthcare Private Limited, and it is classified as Device Class Class B. The approving authority is Gujarat.

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
CK-MB
UID: MFG/MD/2018/000023_8a863ab9781ae23a57fffc35f97a621d_297d816ab4539b867ee7bb8e92de8832

Brand Name

AUTOPAK™

Device Class

Class B

Approving Authority

Gujarat

Product Information

For in vitro diagnostics use in quantitative determination of Total CK-MB in serum using clinical chemistry analyzer

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