Device typeToxoplasma gondii immunoglobulin M (IgM) antibody IVD, kit, fluorescent immunoassay: A collection of reagents and other associated materials intended to be used for the qualitative and/or quantitative detection of immunoglobulin M (IgM) antibodies to the parasitic protozoan Toxoplasma gondii in a clinical specimen, using a fluorescent immunoassay method.
FDA categoryAntigen, Iha, Cytomegalovirus
Device ID00817273020020
MRI safetyLabeling does not contain MRI Safety Information