The OXY Rapid Test is an immunochromatography based one step in vitro test. It is designed for qualitative determination of oxycodone in human urine specimens above a cut-off level of 100 ng/mL. This assay has not been evaluated in the point of care location and is for use by Healthcare Professionals only.
The test device should be stored at 2 to 30°C and will be effective until the expiration date stated on the package. The product is humidity-sensitive and should be used immediately after being open. Any improperly sealed product should be disstriped.
The cut-off concentration (sensitivity level) of OXY test is determined to be 100 ng/ml.