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Test for Progesterone - India CDSCO Medical Device Registration

Test for Progesterone is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2020/000618_1c41e697f9be20f3acbfac837d0a9720_5ae283c1076b25da80cddd5ce5605280. 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 Progesterone
UID: IMP/IVD/2020/000618_1c41e697f9be20f3acbfac837d0a9720_5ae283c1076b25da80cddd5ce5605280

Brand Name

ichroma™ Cystatin C

Device Class

Class B

Approving Authority

CDSCO

Product Information

ichroma™ Progesterone is a fluorescence Immunoassay (ichroma™ Cystatin C) for the quantitative determination of progesterone in human serum/plasma. It is useful as an aid in management and monitoring of the cause of infertility, track ovulation, diagnose an ectopic or failing pregnancy, monitor the health of a pregnancy

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