LH FIA Test - India CDSCO Medical Device Registration
LH FIA Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2021/000062_ba72d31bfe86690ad648199a3e28eb1e_5fdeefb5fcf2261bf8b79ba38f217c56. This device is marketed under the brand name hCG. The license holder is Mylab Discovery Solutions Pvt. Ltd. Lonavla, and it is classified as Device Class Class B. The approving authority is Pune Division.
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Brand Name
hCG
License Holder
Mylab Discovery Solutions Pvt. Ltd. LonavlaDevice Class
Approving Authority
Pune Division
Product Information
LH FIA Test is a fluorescent immunoassay to measure LH level in human serum, plasma, and whole blood. The quantitative measurement of the LH helps evaluate fertility issues, function of reproductive organs (hCG), to detect the ovulation to evaluate pituitary function, or to evaluate early or delayed sexual maturation (hCG) in children
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