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/2022/000035_17f7b96ee8e089459c1b11fdab28d0ba_ed6182956032ea6776241a7f3a01cce2. The license holder is DIYA SCIENTIFIC, and it is classified as Device Class Class B. The approving authority is CDSCO.
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License Holder
DIYA SCIENTIFICDevice Class
Approving Authority
CDSCO
Product Information
The Biotime AMH Rapid Quantitative Test is intended to quantify the concentration of AMH##PLACEHOLDER_0## in human serum or plasma on Biotime FIA Analyzer by fluorescent immunoassay. The test is used as an aid detection of ovary function and fertility assessment. -Fluorescence immunoassay -Ovary function and fertility For in vitro diagnostic use only. For professional use only
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