Device typeFree estriol (oestriol) IVD, kit, chemiluminescent immunoassay: A collection of reagents and other associated materials intended to be used for the qualitative and/or quantitative detection of free estriol (oestriol) in a clinical specimen, using a chemiluminescent immunoassay method. It is typically measured in maternal blood or urine as a marker of foetal health, gestational age, or fetoplacental distress typically in pregnancies complicated by diabetes, hypertension, or prolonged gestation.
FDA categoryRadioimmunoassay, Estriol
Device ID00840239016126
Catalog numberEIA-1612
AvailabilityPrescription
Single useYes
MRI safetyLabeling does not contain MRI Safety Information