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Anti-Mullerian hormone Test - India CDSCO Medical Device Registration

Anti-Mullerian hormone Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2023/000103_a3e37ec956880c2bab8372e2f3e1d7d1_3e32d169ee6cdbfdb63702f6a477379c. This device is marketed under the brand name RF-IgM. The license holder is Genovik Biotech Pvt. Ltd., and it is classified as Device Class Class B. The approving authority is Rajasthan.

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 Test
UID: MFG/IVD/2023/000103_a3e37ec956880c2bab8372e2f3e1d7d1_3e32d169ee6cdbfdb63702f6a477379c

Brand Name

RF-IgM

Device Class

Class B

Approving Authority

Rajasthan

Product Information

Genovik Anti-Mullerian hormone (RF-IgM) is applicable to the quantitative detection of the concentration of Anti-Mullerian hormone (RF-IgM) in human serum or plasma

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