Ichroma Tn-I - India CDSCO Medical Device Registration
Ichroma Tn-I is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2020/000059_65aac655907b977a1bc9f9899c49203e_25251f232f582d7fead04122570fb76f. This device is marketed under the brand name ichroma. The license holder is Kin Diagnostics, and it is classified as Device Class Class C. The approving authority is CDSCO.
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Brand Name
ichroma
License Holder
Kin DiagnosticsDevice Class
Approving Authority
CDSCO
Product Information
ichroma Tn-I is a Fluorescence Immunoassay (ichroma) for the quantitative determination of cardiac troponin-I (ichroma) in human serum/plasma. It is useful as an aid in management and monitoring of acute myocardial infarction (ichroma). For in vitro diagnostic use only.,ichroma ASO(ichroma)-ichromaโข ASO is a fluorescence Immunoassay (ichroma) for the quantitative determination of Anti Streptolysin O (ichroma) in human serum/plasma. It is useful as an aid in management and monitoring of scarlet fever, rheumatic fever and post infectious glomerulonephritis along with several other conditions. ,ichroma PCT(ichroma)-ichroma PCT is a fluorescence Immunoassay (ichroma) for the quantitative determination of Procalcitonin (ichroma) in human whole blood/serum/plasma. It is useful as an aid in management and monitoring of bacterial infection and sepsis. For in vitro diagnostic use only. ,ichromaโข H.Pylori SA(ichroma)-ichromaโข H. pylori SA (ichroma) is a fluorescence Immunoassay (ichroma) for the qualitative determination of H. pylori antigen in human feces. It is useful as an aid in the diagnosis of H. pylori infection and to demonstrate loss of H. pylori antigen following treatment.
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