AMH Fast Test Kit - India CDSCO Medical Device Registration

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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CDSCO Registered

Class Class B

AMH Fast Test Kit

UID: IMP/IVD/2022/000153_63c2d5aa50a9729120db816087919884_2ae6d3d78aca5fb12f4f289d9c909e5c

Brand Name

Immunofluorescence Assay

License Holder

Cipla Limited

Device Class

Class B

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