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CDSCO UID IMP/IVD/2021/000395_5402c1da55540d1cb9c6be8c83a04c00_896dedf7e9c64dc5716c303d961519b2

Myo Rapid Quantitative Test

M/s Vishat Diagnostic Pvt Ltd.·Device Class Class B·India CDSCO·Brand: Biotime
Registration details
UID
IMP/IVD/2021/000395_5402c1da55540d1cb9c6be8c83a04c00_896dedf7e9c64dc5716c303d961519b2
Device class
Class B
Brand name
Biotime
License holder
M/s Vishat Diagnostic Pvt Ltd.
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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About this record

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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