CDSCO UID IMP/IVD/2020/000383_cc2c1703bdb8a4a13f0d2a482d112faf_1a1a703e09daedd82c1bf8482875d14e

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

BIODX HEALTHCARE·Device Class Class C·India CDSCO·Brand: Immunofluorescence

Registration details

UID: IMP/IVD/2020/000383_cc2c1703bdb8a4a13f0d2a482d112faf_1a1a703e09daedd82c1bf8482875d14e
Device class: Class C
Brand name: Immunofluorescence
License holder: BIODX HEALTHCARE
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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About this record

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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