CK-MB Rapid Quantitative Test - India CDSCO Medical Device Registration
CK-MB Rapid Quantitative Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2022/000035_839efcc2b83906b56051f06e33530ec2_b905c589b8e97f64ba9e9f71306c3001. The license holder is DIYA SCIENTIFIC, and it is classified as Device Class Class B. The approving authority is CDSCO.
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License Holder
DIYA SCIENTIFICDevice Class
Approving Authority
CDSCO
Product Information
The Biotime CK-MB ##PLACEHOLDER_0## Rapid Quantitative Test is intended to quantify the concentration of CK-MB in human serum or plasma on Biotime FIA Analyzer by fluorescent immunoassay. It is used as an aid detection of acute myocardial infarction
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