LH Fast Test Kit - India CDSCO Medical Device Registration

LH Fast Test Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2022/000153_5a8e1009247845488ee45ac2790fd328_03f3206062adf087a1ef7ad0bdb0eda9. 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

LH Fast Test Kit

UID: IMP/IVD/2022/000153_5a8e1009247845488ee45ac2790fd328_03f3206062adf087a1ef7ad0bdb0eda9

Brand Name

Immunofluorescence Assay

License Holder

Cipla Limited

Device Class

Class B

Approving Authority

CDSCO

Product Information

LH Fast Test Kit (Immunofluorescence Assay) is intended for in vitro quantitative determination of LH in human serum and plasma. This test is used to determine menopause, pinpoint ovulation and monitor endocrine therapy