Intended Use
The Tramadol Rapid Test are immunochromatography based one step in vitro test. It is designed for qualitative determination of drug substances in human urine specimens. The tests are intended for use by Healthcare Professionals only.
Storage
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 discarded.
Sensitivity
The cut-off concentrations (sensitivity level) of The Tramadol Rapid Test are determined to be: TRA 200 ng/ml.
Citations
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Lelievre, B; Bretaudeau, M; et al. IMMUNOCHROMATOGRAPHIC TESTS: FALSE-POSITIVE RESULTS FOR METHADONE AND PHENCYCLIDINE AFTER ACUTE POISONING WITH TRAMADOL AND DEXTROPROPOXYPHENE. ACTA CLINICA BELGICA 65:12-17(2010).
Zhang, LZ; Guo, Z; et al. Tramadol reduces myocardial infarct size and expression and activation of nuclear factor kappa B in acute myocardial infarction in rats. EUROPEAN JOURNAL OF ANAESTHESIOLOGY 26:1048-1055(2009).
COA
Certificate of Analysis
