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Creatine Kinase and CKMB test reagents/kits - India CDSCO Medical Device Registration

Creatine Kinase and CKMB test reagents/kits is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2023/000034_c9666a3166b6e8cfef744c2078376d70_f6291cba6cbbfe68cf7b85df9742ef2f. This device is marketed under the brand name hCG. The license holder is Sunwest Bio Medical Pvt. Ltd., and it is classified as Device Class Class B. The approving authority is Haryana.

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 and CKMB test reagents/kits
UID: MFG/IVD/2023/000034_c9666a3166b6e8cfef744c2078376d70_f6291cba6cbbfe68cf7b85df9742ef2f

Brand Name

hCG

Device Class

Class B

Approving Authority

Haryana

Product Information

CKMB test reagent/kit are medical devices intended for the estimation of CKMB in blood / body fluids

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