CDSCO UID IMP/IVD/2020/000278_17f7b96ee8e089459c1b11fdab28d0ba_f9bfbf41f25e79ae7bc175d752dd7885

AMH Rapid Quantitative Test

RAPID DIAGNOSTIC PVT. LTD.·Device Class Class B·India CDSCO
Registration details
UID
IMP/IVD/2020/000278_17f7b96ee8e089459c1b11fdab28d0ba_f9bfbf41f25e79ae7bc175d752dd7885
Device class
Class B
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##
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About this record

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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