The STERIS Device Testing program was founded in 1989 to support Customers reprocessing their devices in STERIS's flagship liquid chemical sterilant processing system. The program now includes the V-PRO® Sterilizers, SYSTEM 1E® Liquid Chemical Sterilant Processing System, SYSTEM 1® endo Liquid Chemical Sterilant Processing System, Revital-Ox™ RESERT® High Level Disinfectant and the Reliance® EPS Endoscope Reprocessing Systems. The STERIS Device Testing team collaborates closely with medical device manufacturers to validate devices for use in STERIS's low temperature reprocessing portfolio, minimizing risk and providing confidence in your process. The world of device reprocessing is getting busier and more visible than ever before. The STERIS Device Testing team is here to support you and help you reprocess your devices with confidence using STERIS's low temperature reprocessing solutions.
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