Test for total beta human chorionic gonadotropin - India CDSCO Medical Device Registration

Test for total beta human chorionic gonadotropin is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2020/000618_7dec4eaf7386264742ddfd3f3275e446_0a95d8f3beffa7966757d17028f56b8a. 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.

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CDSCO Registered

Class Class B

Test for total beta human chorionic gonadotropin

UID: IMP/IVD/2020/000618_7dec4eaf7386264742ddfd3f3275e446_0a95d8f3beffa7966757d17028f56b8a

Brand Name

ichroma™ Cystatin C

License Holder

KABS HEALTHCARE PRIVATE LIMITED

Device Class

Class B

Approving Authority

CDSCO

Product Information

ichroma™ β-HCG is a fluorescence Immunoassay (ichroma™ Cystatin C) for the quantitative determination of total β-hCG in human whole blood/serum/plasma. It is useful as an aid in management and monitoring of total beta human chorionic gonadotropin (ichroma™ Cystatin C) level in human

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Test for total beta human chorionic gonadotropin

Brand: QDx Instacheck™ Cortisol

DiaSys Diagnostics India Private Limited

Test for total beta human chorionic gonadotropin - India CDSCO Medical Device Registration

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Approving Authority

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