LH Test - India CDSCO Medical Device Registration
LH Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2021/000413_d68f41bd21b2a1e6da866d50ae5cd82e_ddcddb1b5b4e76be22acf396f189e281. This device is marketed under the brand name Finecare Beta-HCG Rapid Quantitative Test. The license holder is Star Biomed Pvt. Ltd., and it is classified as Device Class Class B. The approving authority is CDSCO.
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Brand Name
Finecare Beta-HCG Rapid Quantitative Test
License Holder
Star Biomed Pvt. Ltd.Device Class
Approving Authority
CDSCO
Product Information
The Finecare™ LH Rapid Quantitative Test is a fluorescence immunoassay used along with Finecare™ FIA System (Finecare Beta-HCG Rapid Quantitative Test) for quantitative determination of Luteinizing hormone (Finecare Beta-HCG Rapid Quantitative Test) in human whole blood, serum or plasma
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