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Ultrasensitive C-Reactive Protein Kit - India CDSCO Medical Device Registration

Ultrasensitive C-Reactive Protein Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2020/000671_ca15797fed8b388a2e7b371f841751e7_d21752833113ba0d8614b63c141ad2b4. 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
Ultrasensitive C-Reactive Protein Kit
UID: IMP/IVD/2020/000671_ca15797fed8b388a2e7b371f841751e7_d21752833113ba0d8614b63c141ad2b4

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 Ultrasensitive C-Reactive Protein (UsCRP Kit) in human serum or plasma as an aid in diagnosis and monitoring of inflammatory conditions, bacterial infection as well as cardiac diseases

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