Device typeUrea IVD, control: A material which is used to verify the performance of an assay intended to be used for the qualitative and/or quantitative detection of urea or urea nitrogen [also known as blood urea nitrogen (BUN)] in a clinical specimen.
FDA categoryUrease And Glutamic Dehydrogenase, Urea Nitrogen
Device ID00817274020951
MRI safetyLabeling does not contain MRI Safety Information