CRP Rapid Quantitative Test - India CDSCO Medical Device Registration
CRP Rapid Quantitative Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2022/000035_36b9d76978b5275b7f9b27dc2d352407_615ceb28c1182b63e5a25e5f3de91556. The license holder is DIYA SCIENTIFIC, and it is classified as Device Class Class C. The approving authority is CDSCO.
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License Holder
DIYA SCIENTIFICDevice Class
Approving Authority
CDSCO
Product Information
The Biotime CRP Rapid Quantitative Test is intended to quantify the concentration of CRP, including high-sensitivity CRP##PLACEHOLDER_0## and normal CRP in human serum, plasma or whole blood on Biotime FIA Analyzers by fluorescent immunoasay. The test is used as an aid detection of infectious processes, hsCRP is also used as an aid detection of cardiovascular disease
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