SARS-CoV-2 IgM/IgG Antibody Assay Kit (SARS-CoV-2 IgM/IgG Antibody Assay Kit ) - India CDSCO Medical Device Registration

SARS-CoV-2 IgM/IgG Antibody Assay Kit (SARS-CoV-2 IgM/IgG Antibody Assay Kit ) is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2020/000383_cc2c1703bdb8a4a13f0d2a482d112faf_1a1a703e09daedd82c1bf8482875d14e. This device is marketed under the brand name Immunofluorescence. The license holder is BIODX HEALTHCARE, and it is classified as Device Class Class C. The approving authority is CDSCO.

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CDSCO Registered

Class Class C

SARS-CoV-2 IgM/IgG Antibody Assay Kit (SARS-CoV-2 IgM/IgG Antibody Assay Kit )

UID: IMP/IVD/2020/000383_cc2c1703bdb8a4a13f0d2a482d112faf_1a1a703e09daedd82c1bf8482875d14e

Brand Name

Immunofluorescence

License Holder

BIODX HEALTHCARE

Device Class

Class C

Approving Authority

CDSCO

Product Information

This kit is used for the qualitative detection of specific IgM antibodies and IgG antibodies against novel coronavirus (Immunofluorescence) in human specimens (Immunofluorescence)

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