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Sample Type
Human Plasma Sample
Specialty
Requires Refrigeration
Storage Requirements
Homogenous Enzyme Immunoassay (HEIA)
Test Category
Mycophenolic Acid
Test Method
Therapeutic Drug Monitoring
Test Name
41116007
UNSPSC Code
R1: 11 mL
Volume
R2: 26 mL
Features
The CEDIA® Mycophenolic Acid (MPA) Assay is an in vitro diagnostic medical device intended for the quantitative measurement of mycophenolic acid in human plasma using automated clinical chemistry analyzers as an aid in the management of mycophenolic acid therapy in renal and cardiac transplant patients