The information in the device guide identifies those cleaned, immersible, reusable, critical and semi-critical, heat sensitive medical devices and accessories that have been tested to confirm materials compatibility as well as efficacy by STERIS's Device Testing Program and/or the device manufacturer with the SYSTEM 1E Liquid Chemical Sterilant Processing System.
The following information identifies those cleaned, reusable, immersible, critical and semi-critical, heat-sensitive medical devices that have been validated by STERIS Corporation for processing in the SYSTEM 1E® Processor. Do NOT process any device in the SYSTEM 1E Processor that (1) is not listed in this Quick Connect Finder, or (2) the device manufacturer has labeled as not suitable for processing in the SYSTEM 1E Processor or in liquid chemical sterilization systems. 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 Quick Connects and the SYSTEM 1E Processor when processing validated devices in the SYSTEM 1E Processor.