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The information in this device matrix identifies semi-critical devices and accessories that have been validated for reprocessing in the Reliance EPS Endoscope Processing System by STERIS's Device testing Program and the device manufacturer.
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The following information identifies those manually pre-cleaned, immersible, reusable, heat sensitive, semi-critical medical devices and related accessories that have been validated by STERIS Corporation for processing in the Reliance® EPS Endoscope Processing System. Do NOT process any device or related accessory in the Reliance EPS Processor that (1) is not listed in this Online Guide, or (2) the device manufacturer has labeled as not suitable for processing in the Reliance EPS Processor. This site updates frequently. Consult and follow the device manufacturer's labeling and instructions for use for all processing, cleaning, handling and maintenance instructions. Consult and follow all product labeling and instructions for use for Flow Units, accessories, and the Reliance EPS Processor when processing validated devices and accessories in the Reliance EPS Endoscope Processing System.