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Anti-Mullerian Hormone ELISA test Kit - India CDSCO Medical Device Registration

Anti-Mullerian Hormone ELISA test Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000060_edd102b572f3fc6fc0a1f4591b33699e_a8d000c598f9801173ffe93036f633f6. This device is marketed under the brand name EIA. The license holder is Genomix Molecular Diagnostics Pvt Ltd, and it is classified as Device Class Class B. The approving authority is Telangana.

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
Anti-Mullerian Hormone ELISA test Kit
UID: MFG/IVD/2020/000060_edd102b572f3fc6fc0a1f4591b33699e_a8d000c598f9801173ffe93036f633f6

Brand Name

EIA

Device Class

Class B

Approving Authority

Telangana

Product Information

For the quantitative measurement of AMH in human serum and plasma

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