Device typeUrea 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 urea or urea nitrogen [also known as blood urea nitrogen (BUN)] in a clinical specimen.
FDA categoryBerthelot Indophenol, Urea Nitrogen
Device ID10673486001273
Catalog numberB551-132
AvailabilityPrescription
MRI safetyLabeling does not contain MRI Safety Information