Device typeListeria monocytogenes antigen IVD, reagent: A substance or reactant intended to be used together with a parent IVD to perform a specific function in an assay that is used for the qualitative and/or quantitative detection of antigens from Listeria monocytogenes bacteria in a clinical specimen.
FDA categoryANTISERA, ALL TYPES, LISTERIA MONOCYTOGENES
Device ID00382902230113
Catalog number223011
AvailabilityPrescription
Single useYes
LatexContains natural rubber latex
MRI safetyLabeling does not contain MRI Safety Information
Total Volume1 Milliliter