Device typeMyeloperoxidase anti-neutrophil cytoplasmic antibody (MPO-ANCA) IVD, kit, enzyme immunoassay (EIA): A collection of reagents and other associated materials intended to be used for the qualitative and/or quantitative detection of anti-neutrophil cytoplasmic antibodies (ANCA) to myeloperoxidase (MPO) in a clinical specimen, using an enzyme immunoassay (EIA) method.
FDA categoryTEST SYSTEM, ANTINEUTROPHIL CYTOPLASMIC ANTIBODIES (ANCA)
Device ID04048474035971
Catalog numberEIA-3597
AvailabilityPrescription
Single useYes
MRI safetyLabeling does not contain MRI Safety Information