Details
Device typeTrichomonas vaginalis antigen IVD, kit, rapid ICT, clinical: A collection of reagents and other associated materials intended to be used for the qualitative and/or (semi-)quantitative detection of antigens from the parasitic protozoan Trichomonas vaginalis in a clinical specimen within a short period, relative to standard laboratory testing procedures, using an immunochromatographic test (ICT) method [lateral flow test]. This is a rapid test used in the laboratory or in point-of-care analyses. It is not intended to be used for self-testing.
FDA categoryKIT, SCREENING, TRICHOMONAS
Device ID00742860100123
Catalog number181-5
AvailabilityPrescription
Single useYes
MRI safetyLabeling does not contain MRI Safety Information