CDSCO UID IMP/IVD/2022/000153_63c2d5aa50a9729120db816087919884_2ae6d3d78aca5fb12f4f289d9c909e5c

AMH Fast Test Kit

Cipla Limited·Device Class Class B·India CDSCO·Brand: Immunofluorescence Assay
Registration details
UID
IMP/IVD/2022/000153_63c2d5aa50a9729120db816087919884_2ae6d3d78aca5fb12f4f289d9c909e5c
Device class
Class B
Brand name
Immunofluorescence Assay
License holder
Cipla Limited
Approving authority
CDSCO
Product information
AMH Fast Test Kit (Immunofluorescence Assay) is intended for in vitro quantitative determination of AMH in human serum and plasma samples. This test can be used as an aid in indicating ovarian functional reserve, and also help to diagnose menstrual disorders or to monitor the health of women
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About this record

AMH Fast Test Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2022/000153_63c2d5aa50a9729120db816087919884_2ae6d3d78aca5fb12f4f289d9c909e5c. This device is marketed under the brand name Immunofluorescence Assay. The license holder is Cipla Limited, and it is classified as Device Class Class B. The approving authority is CDSCO.

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