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Test for cystatin C - India CDSCO Medical Device Registration

Test for cystatin C is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2019/000074_abc2e5d2f99faad4f72a6a606e2be597_8dec00cd703cd9441cfdc45c98f8fa7f. This device is marketed under the brand name ichroma™ T4. The license holder is Inkarp Instruments Pvt. Ltd., and it is classified as Device Class Class B. 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 B
Test for cystatin C
UID: IMP/IVD/2019/000074_abc2e5d2f99faad4f72a6a606e2be597_8dec00cd703cd9441cfdc45c98f8fa7f

Brand Name

ichroma™ T4

Device Class

Class B

Approving Authority

CDSCO

Product Information

ichroma™ Cystatin C is a fluorescence Immunoassay (ichroma™ T4) for the quantitative determination of cystatin C in human serum/plasma. It is useful as an aid in management and monitoring of renal disease. For in vitro diagnostic use only

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