FSH Test - India CDSCO Medical Device Registration
FSH Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2021/000413_ac2de8f3a56279f65230475155fad89b_3bb6a3cb57a1c81c6385c9245897cec5. 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™ FSH Rapid Quantitative Test is a fluorescence immunoassay used along with Finecare™ FIA System (Finecare Beta-HCG Rapid Quantitative Test) for quantitative measurement of follicle-stimulating hormone (Finecare Beta-HCG Rapid Quantitative Test) in human whole blood, serum or plasma
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