Device typeCeruloplasmin IVD, kit, nephelometry/turbidimetry: A collection of reagents and other associated materials intended to be used for the quantitative measurement of ceruloplasmin in a clinical specimen, using a nephelometry/turbidimetry method.
FDA categoryINDIRECT COPPER ASSAY, CERULOPLASMIN
Device ID00380740010829
Catalog number06K9130
AvailabilityPrescription
MRI safetyLabeling does not contain MRI Safety Information