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CRP - India CDSCO Medical Device Registration

CRP is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2021/000121_68e5ed3321d8b86d30dd340193dc3716_71b62b429db584ef6f4b376dc78c3414. The license holder is Promea Therapeutics Private Limited, and it is classified as Device Class Class C. The approving authority is CDSCO, Zonal office, Hyderabad.

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
CRP
UID: MFG/IVD/2021/000121_68e5ed3321d8b86d30dd340193dc3716_71b62b429db584ef6f4b376dc78c3414

Device Class

Class C

Approving Authority

CDSCO, Zonal office, Hyderabad

Product Information

CRP testing kit is used to detect the CRP concentration in human plasma or serum by quantitative method.

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