Diagnostic Kit for IgM/IgG Antibody to Coronavirus - India CDSCO Medical Device Registration
Diagnostic Kit for IgM/IgG Antibody to Coronavirus is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2020/000351_57ce9ce0b764ee7140ef0baaad24c4e5_b22f07a9e6968eda7694be95954faa65. This device is marketed under the brand name SARS-CoV-2. The license holder is Renaissance Pharmaceuticals, and it is classified as Device Class Class C. The approving authority is CDSCO.
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Brand Name
SARS-CoV-2
License Holder
Renaissance PharmaceuticalsDevice Class
Approving Authority
CDSCO
Product Information
This product is used for in vitro qualitative detection of Coronavirus (SARS-CoV-2) IgM/IgG antibody in human serum, plasma and venous whole blood samples.
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