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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 IMP/IVD/2019/000039_68e5ed3321d8b86d30dd340193dc3716_fbfda3a2cb2b72751a36dac8d0f4bff3. This device is marketed under the brand name PCT Rapid Quantitative Test. The license holder is M/s Avantor Performance Materials India Ltd, 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
CRP
UID: IMP/IVD/2019/000039_68e5ed3321d8b86d30dd340193dc3716_fbfda3a2cb2b72751a36dac8d0f4bff3

Brand Name

PCT Rapid Quantitative Test

Device Class

Class C

Approving Authority

CDSCO

Product Information

Quantitative determination of CRP in human whole blood, serum or plasma. The test is used as an aid to predict future cardiovascular diseases (PCT Rapid Quantitative Test) as wellas to see infection and inflammation

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