CRP Test - India CDSCO Medical Device Registration

CRP Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2021/000413_bcd9e8baa7fe12da9e51bf745645464a_73db0a1c8d9eed6f11dc15650b25e714. This device is marketed under the brand name Finecare cTn I/CK-MB/Myo Rapid Quantitative Test. The license holder is Star Biomed Pvt. Ltd., and it is classified as Device Class Class C. The approving authority is CDSCO.

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CDSCO Registered

Class Class C

CRP Test

UID: IMP/IVD/2021/000413_bcd9e8baa7fe12da9e51bf745645464a_73db0a1c8d9eed6f11dc15650b25e714

Brand Name

Finecare cTn I/CK-MB/Myo Rapid Quantitative Test

License Holder

Star Biomed Pvt. Ltd.

Device Class

Class C

Approving Authority

CDSCO

Product Information

The Finecare™ CRP Rapid Quantitative Test is a fluorescence immunoassay used along with Finecare™ FIA System (Finecare cTn I/CK-MB/Myo Rapid Quantitative Test) for quantitative determination of C-reactive protein (Finecare cTn I/CK-MB/Myo Rapid Quantitative Test) in human whole blood, serum or plasma.,cTn I Test(Finecare cTn I/CK-MB/Myo Rapid Quantitative Test)-The Finecare™ cTn I Rapid Quantitative Test is a fluorescence immunoassay used along with Finecare™ FIA System (Finecare cTn I/CK-MB/Myo Rapid Quantitative Test) for quantitative determination of cardiac troponin I (Finecare cTn I/CK-MB/Myo Rapid Quantitative Test) in human whole blood, serum or plasma