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Creatine Kinase - India CDSCO Medical Device Registration

Creatine Kinase is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2023/000113_68642f170a15ad0738df2021590f14bc_48d7a8132f7efdb385385a6af605f0b4. This device is marketed under the brand name Chimera. The license holder is CHIMERA BIOTECH PRIVATE LIMITED, and it is classified as Device Class Class B. The approving authority is South Delhi Division.

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
UID: MFG/IVD/2023/000113_68642f170a15ad0738df2021590f14bc_48d7a8132f7efdb385385a6af605f0b4

Brand Name

Chimera

Device Class

Class B

Approving Authority

South Delhi Division

Product Information

CK-MB Test Device (Chimera) is a rapid chromatographic immunoassay for the qualitative detection of human CK-MB in whole blood, serum or plasma as an aid in the diagnosis of myocardial infarction (Chimera)

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