Total IgE Rapid Quantitative Test - India CDSCO Medical Device Registration
Total IgE Rapid Quantitative Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2022/000035_8bd2a368288a785f4e130c4676dff9ff_9b3bf78d51c58ed7fb1adcf7598b699b. 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 total IgE Rapid Quantitative Test is intended to quantify the concentration of total IgE ##PLACEHOLDER_0## in human serum, plasma and whole blood, serum on Biotime FIA Analyzer by fluorescent immunoassay. The test is used as an aid detection of allergic diseases. -Fluorescence immunoassay -Allergic diseases For in vitro diagnostic use only. For professional use only
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