Beta-HCG Rapid Quantitative Test
- UID
- IMP/IVD/2022/000074_7bfb808c451c3f9285d9a37de2b44fa4_c92de77809a74874ef373dd7697202fb
- Device class
- Class C
- Brand name
- Cardiac Troponin T
- License holder
- FINOVA HEALTHCARE PRIVATE LIMITED
- Approving authority
- CDSCO
- Product information
- The β-hCG Rapid Quantitative Test along with Aehealth Fluorescence Immunoassay Analyzer (Cardiac Troponin T) is intended for vitro quantitative determination of β-hCG in human whole blood, serum or plasma. This test used as an aid in the early detection of pregnancy.,cTnI/CK-MB/MYO (Cardiac Troponin T) Rapid Quantitative Test (Cardiac Troponin T)(Cardiac Troponin T)-The Cardiac Troponin I/CK-MB/Myoglobin Rapid Quantitative Test along with Aehealth Fluorescence Immunoassay Analyzer (Cardiac Troponin T) is intended for in vitro quantitative determination of Cardiac Troponin I/CKMB/ Myoglobin in human whole blood, serum or plasma. It is mainly used for Auxiliary diagnosis of myocardial infarction, myopathy and other diseases.,cTnI (Cardiac Troponin T) Rapid Quantitative Test (Cardiac Troponin T)(Cardiac Troponin T)-The cTnI (Cardiac Troponin T) Rapid Quantitative Test along with Aehealth Fluorescence Immunoassay Analyzer is intended for vitro quantitative determination of Cardiac troponin I (Cardiac Troponin T) in human whole blood, serum or plasma. It is mainly used for auxiliary diagnosis of myocardial infarction
Beta-HCG Rapid Quantitative Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2022/000074_7bfb808c451c3f9285d9a37de2b44fa4_c92de77809a74874ef373dd7697202fb. This device is marketed under the brand name Cardiac Troponin T. The license holder is FINOVA HEALTHCARE PRIVATE LIMITED, and it is classified as Device Class Class C. The approving authority is CDSCO.
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