Device typeRickettsia conorii 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 Rickettsia conorii in a clinical specimen, using a fluorescent immunoassay method. The assay is designed to detect infection with Rickettsia conorii, the rickettsial bacteria from the Spotted Fever Group.
FDA categoryAntiserum, Typhus Fever
Device ID20816101020250
Catalog numberIF0100M
AvailabilityPrescription
MRI safetyLabeling does not contain MRI Safety Information