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AMH - India CDSCO Medical Device Registration

AMH is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2020/000059_ef72c09bacb6663782384c46c149c0aa_7d50d2210db15e17e51b26fec965035f. This device is marketed under the brand name ichroma™ ST2. The license holder is Kin Diagnostics, 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
AMH
UID: IMP/IVD/2020/000059_ef72c09bacb6663782384c46c149c0aa_7d50d2210db15e17e51b26fec965035f

Brand Name

ichroma™ ST2

License Holder

Kin Diagnostics

Device Class

Class B

Approving Authority

CDSCO

Product Information

ichroma™ AMH is a fluorescence Immunoassay (ichroma™ ST2) for the quantitative determination of AMH (ichroma™ ST2) in human serum/plasma. It is useful as an aid in management and monitoring of premature ovarian insufficiency, menopause and ovarian reserve. For in vitro diagnostic use only

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