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Test for Luteinizing hormone - India CDSCO Medical Device Registration

Test for Luteinizing hormone is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2020/000618_9a702b5ab814b0f556015538b5b1038a_f9b44a8e743672b1855789f78a053a9b. This device is marketed under the brand name ichroma™ Cystatin C. The license holder is KABS HEALTHCARE PRIVATE LIMITED, 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 Luteinizing hormone
UID: IMP/IVD/2020/000618_9a702b5ab814b0f556015538b5b1038a_f9b44a8e743672b1855789f78a053a9b

Brand Name

ichroma™ Cystatin C

Device Class

Class B

Approving Authority

CDSCO

Product Information

ichroma™ LH is a fluorescence Immunoassay (ichroma™ Cystatin C) for the quantitative determination of Luteinizing hormone (ichroma™ Cystatin C) in human serum/plasma. It is useful as an aid in management and monitoring of determination of evaluating fertility issues, function of reproductive organs (ichroma™ Cystatin C), or detection of the ovulation

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