AMH Rapid Quantitative Test - India CDSCO Medical Device Registration
AMH Rapid Quantitative Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2020/000278_17f7b96ee8e089459c1b11fdab28d0ba_f9bfbf41f25e79ae7bc175d752dd7885. The license holder is RAPID DIAGNOSTIC PVT. LTD., and it is classified as Device Class Class B. The approving authority is CDSCO.
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License Holder
RAPID DIAGNOSTIC PVT. LTD.Device Class
Approving Authority
CDSCO
Product Information
The Finecare AMH Rapid Quantitative Test is a fluorescence immunoassay used along with Finecare FIA Meters ##PLACEHOLDER_0## 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 ##PLACEHOLDER_0##
