The information in the device guide identifies those cleaned, immersible, reusable, semi-critical, heat sensitive medical devices and accessories that have been tested by STERIS's Device Testing Program and/or the device manufacturer to confirm materials compatibility as well as efficacy with the SYSTEM 1® endo Liquid Chemical Sterilant Processing System.
The following information identifies those cleaned, reusable, immersible, semi-critical, heat-sensitive medical devices that have been validated by STERIS Corporation for processing in the SYSTEM 1® endo Processor. Do NOT process any device in the SYSTEM 1® endo 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 1® endo Processor or by liquid chemical sterilization. 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 1® endo Processor when processing validated devices in the SYSTEM 1® endo Processor.