Progesterone reagent 07M4875A

serumplasmadiagnostic

The Progesterone Chemiluminescence Immunoassay kit is intended for the measurement of Progesterone concentration in human serum or plasma. Usage Statement FDA cleared for In Vitro Diagnostic (IVD) use in the United States. CE Marked for IVD use outside the United States. Analyte / Target - Progesterone Base Catalog Number - M4875A Diagnostic Platforms - ChLIA Diagnostic Solutions - Endocrinology Disease Screened - Progesterone Evaluation - Quantitative Pack Size - 1 96 Wells Sample Type - Plasma, Serum Sample Volume - 25 µL Sensitivity - 0.105 ng/mL Species Reactivity - Human Usage Statement - FDA cleared for In Vitro Diagnostic (IVD) use in the United States. CE Marked for IVD use outside the United States.