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CDSCO UID MFG/IVD/2022/000064_21a8abae789681a61d85f80bd9d61343_e7eb162e43a9c685e48028817b673ebf

Diagnostics test reagent / kits cTnI Test Kit

M/s Allied Biotechnology India Pvt Ltd·Device Class Class C·India CDSCO·Brand: Dry Fluorescence Immunoassay
Registration details
UID
MFG/IVD/2022/000064_21a8abae789681a61d85f80bd9d61343_e7eb162e43a9c685e48028817b673ebf
Device class
Class C
Brand name
Dry Fluorescence Immunoassay
License holder
M/s Allied Biotechnology India Pvt Ltd
Approving authority
Central Drug Standards Control Organization, West Zone
Product information
cTnI Test Kit (Dry Fluorescence Immunoassay) is intended for in-vitro quantitative measurement of cTnI (Dry Fluorescence Immunoassay) in serum and plasma. This test is used as an aid in the diagnosis of myocardial injury such as Acute Myocardial Infarction (Dry Fluorescence Immunoassay), Unstable Angina, Acute Myocarditis and Acute Coronary Syndrome (Dry Fluorescence Immunoassay)
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About this record

Diagnostics test reagent / kits cTnI Test Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000064_21a8abae789681a61d85f80bd9d61343_e7eb162e43a9c685e48028817b673ebf. This device is marketed under the brand name Dry Fluorescence Immunoassay. The license holder is M/s Allied Biotechnology India Pvt Ltd, and it is classified as Device Class Class C. The approving authority is Central Drug Standards Control Organization, West Zone.

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