Beta-HCG Rapid Quantitative Test - India CDSCO Medical Device Registration

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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CDSCO Registered

Class Class C

Beta-HCG Rapid Quantitative Test

UID: IMP/IVD/2022/000074_7bfb808c451c3f9285d9a37de2b44fa4_c92de77809a74874ef373dd7697202fb

Brand Name

Cardiac Troponin T

License Holder

FINOVA HEALTHCARE PRIVATE LIMITED

Device Class

Class C

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