Covid - India CDSCO Medical Device Registration
Covid is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2020/001116_ea58c37c7efc6be13b96d8d9957155d7_9a31510211c6d899809c10e4a38d05ae. The license holder is ADVY CHEMICAL PVT. LTD., and it is classified as Device Class Class C. The approving authority is CDSCO.
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License Holder
ADVY CHEMICAL PVT. LTD.Device Class
Approving Authority
CDSCO
Product Information
19 IgG/IgM antibody test Uncut sheet-EzDx COVID-19 antibody detection rapid kit is a rapid and qualitative immune-chromatographic in vitro assay for the differential detection of IgM & IgG antibodies to COVID-19 virus in human serum, plasma/whole blood samples obtained from patient with signs and symptoms of respiratory infection. It is designed for qualitative detection of Immunoglobulin G and Immunoglobulin M antibody of Novel Coronavirus ##PLACEHOLDER_0## in human blood. The test is intended for professional and laboratory use
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Covid-19 Rapid Antigen test for the Qualitative detection of SARS-CoV-2 antigen from nasopharyngeal swab Specimen
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