Myo Rapid Quantitative Test - India CDSCO Medical Device Registration
Myo Rapid Quantitative Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2021/000395_5402c1da55540d1cb9c6be8c83a04c00_896dedf7e9c64dc5716c303d961519b2. This device is marketed under the brand name Biotime . The license holder is M/s Vishat Diagnostic Pvt Ltd., and it is classified as Device Class Class B. The approving authority is CDSCO.
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Brand Name
Biotime
License Holder
M/s Vishat Diagnostic Pvt Ltd.Device Class
Approving Authority
CDSCO
Product Information
The Biotime MYO (Biotime ) Rapid Quantitative Test is intended to quantify the concentration of MYO in human serum or plasma on Biotime FIA Analyzers by fluorescent immunoassay. It is used as an aid detection of acute myocardial infarction
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