Device typeMultiple Leishmania species total antibody IVD, control: A material which is used to verify the performance of an assay intended to be used for the qualitative and/or quantitative detection of total antibodies to multiple species of the parasitic protozoan Leishmania in a clinical specimen.
FDA categoryReagent, Leishmanii Serological
Device ID05391516748926
Catalog number20-04002
Single useYes
MRI safetyLabeling does not contain MRI Safety Information