CK-MB/cTnI/Myo Fast Test Kit
- UID
- IMP/IVD/2019/000410_66cbe1a7376c45ee3d268da5f4979ae9_440c29812bd2d7bf2cdeec5fdcc7d4e4
- Device class
- Class C
- Brand name
- Imumunofluorescence Assay
- License holder
- Vector Biotek Pvt Ltd
- Approving authority
- CDSCO
- Product information
- CK-MB/cTnl/Myo Fast Test Kit (Imumunofluorescence Assay) is intended for in vitro quantitative determination of CK-MB/cTnl/ Myo in serum, plasma or whole blood. This test is used as an aid in the clinical diagnosis, prognosis and evaluation of myocardial injury such as Acute Myocardial Infarction (Imumunofluorescence Assay), Unstable Angina, Acute Myocarditis and Acute Coronary Syndrome (Imumunofluorescence Assay)
CK-MB/cTnI/Myo Fast Test Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2019/000410_66cbe1a7376c45ee3d268da5f4979ae9_440c29812bd2d7bf2cdeec5fdcc7d4e4. This device is marketed under the brand name Imumunofluorescence Assay. The license holder is Vector Biotek Pvt Ltd, and it is classified as Device Class Class C. The approving authority is CDSCO.
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