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Full Range C-Reactive Protein Kit - India CDSCO Medical Device Registration

Full Range C-Reactive Protein Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2020/000671_9f073bfbb4f04fbd695c0f800b7dd459_1d1a6c79645067bb11c33edf44712f0d. This device is marketed under the brand name UsCRP Kit. The license holder is JAINAM BIOMEDICAL, and it is classified as Device Class Class C. 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 C
Full Range C-Reactive Protein Kit
UID: IMP/IVD/2020/000671_9f073bfbb4f04fbd695c0f800b7dd459_1d1a6c79645067bb11c33edf44712f0d

Brand Name

UsCRP Kit

License Holder

JAINAM BIOMEDICAL

Device Class

Class C

Approving Authority

CDSCO

Product Information

This product is used on GPP-100 Specific Protein Analyzer for quantitative determination of Full Range C-Reactive Protein (UsCRP Kit) in human whole blood or serum or plasma as an aid in diagnosis and treatment of inflammatory conditions, bacterial infection as well as cardiac diseases

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