AMH Test
- UID
- IMP/IVD/2019/000191_5338e56adfe6768a730930dfde597a36_b4bd48b366d7fa8e57a443edc893f3cf
- Device class
- Class B
- Brand name
- Testosterone Rapid Quantitative Test
- License holder
- Matrix Labs
- Approving authority
- CDSCO
- Product information
- The FinecareTM AMH Rapid Quantitative Test is a fluorescence immunoassay used along with FinecareTM FIA Meters (Testosterone Rapid Quantitative Test) for quantitative measurement of AMH in human whole blood, serum or plasma. The test is mainly used in the assessment of the ovarian reserve and as an aid in the diagnosis of polycystic ovary syndrome (Testosterone Rapid Quantitative Test)
AMH Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2019/000191_5338e56adfe6768a730930dfde597a36_b4bd48b366d7fa8e57a443edc893f3cf. This device is marketed under the brand name Testosterone Rapid Quantitative Test. The license holder is Matrix Labs, 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.