Device typeSoluble mesothelin-related peptide (SMRP) IVD, kit, chemiluminescent immunoassay: A collection of reagents and other associated materials intended to be used for the qualitative and/or quantitative detection of soluble mesothelin-related peptide (SMRP) in a clinical specimen, using a chemiluminescent immunoassay method. It is typically used as a prognostic marker to monitor the progression or recurrence of mesothelioma.
FDA categoryCancer Monitoring Test System, Soluble Mesothelin-Related Peptides, Epithelioid/Biphasic Mesothelioma
Device ID04987270235157
AvailabilityPrescription
MRI safetyLabeling does not contain MRI Safety Information
SizeSize Type = Tests Per kit; Size Unit = 42; Unit of Measure = Tests