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Test for CRP - India CDSCO Medical Device Registration

Test for CRP is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2019/000074_c512aafa2a2bedba7e26c1231cc15d95_d61ddbdab8fc9c6c707118bf0464305b. This device is marketed under the brand name ichroma™. The license holder is Inkarp Instruments Pvt. 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
Test for CRP
UID: IMP/IVD/2019/000074_c512aafa2a2bedba7e26c1231cc15d95_d61ddbdab8fc9c6c707118bf0464305b

Brand Name

ichroma™

Device Class

Class C

Approving Authority

CDSCO

Product Information

ichroma™ CRP is a fluorescence Immunoassay (ichroma™) for the quantitative determination of CRP in human whole blood/serum/ plasma. It is useful as an aid in management and monitoring of autoimmune diseases and infectious processes, such as rheumatoid arthritis

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