STERIS Low Temperature Reprocessing Device Compatibility Matrix
Enter the Device Model Number In the Search Box below to find out which of the following STERIS Low Temperature Reprocessing Solutions are compatible for processing that specific device.
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If you have a question regarding the appropriate use of a STERIS reprocessing product, please contact STERIS.
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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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Medical Device Manufacturers
STERIS offers a great opportunity to give your products the advantage of being validated for some of the newest and most popular technology in our low temperature portfolio. This also helps to ensure that Customer's reprocessing requirements and needs are met when making purchasing decisions.
The low temperature portfolio from STERIS includes chemistry formulations and processes that are gentle and safe for your devices, patients, users and the environment.
Why work with the STERIS Device Testing?
- Scientific team with decades of experience working with oxidative chemistries and a wide variety of medical devices
- Collaborative evaluation of efficacy, material and functionality compatibility of medical devices being validated
- Consultative team that can provide input on product design or components such as adhesives and anodization to ensure efficacy and material compatibility of the device
- Summary reports and suggested verbiage for updating Instructions for Use provided at the end of all the testing
- All validation testing performed in accordance with ISO 13485:2016 Medical Devices – Quality management systems
Device Validation Request FormGet your devices validated.
Complete the Device Validation Request Form and submit. |
