T4 Test - India CDSCO Medical Device Registration
T4 Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2021/000413_59b407e8a64413fa674221a6d13bc7c1_6c9076c42fe55bb6c49e2fcf8fa6780e. 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 FinecareTM T4 Rapid Quantitative Test is a fluorescence immunoassay used along with Finecare™ FIA System (Finecare Beta-HCG Rapid Quantitative Test) for quantitative determination of Thyroxine (Finecare Beta-HCG Rapid Quantitative Test) in human whole blood, serum or plasma
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