Revox Sterilization Solutions and Cantel Medical are part of the Cantel Medical Corp, a medical device company dedicated to infection prevention and control. The Revox team includes mechanical engineers, chemists, microbiologists, quality assurance and regulatory affairs professionals. The company will work to understand your challenges, concerns and opportunities and provide expert insight to help you decide if Revox sterilization is the right sterilization solution for your product or product concept and/or operational efficiency improvement goals.
Featured technology: Room-temperature vaporized peracetic acid method
- Revox Sterilization Solutions uses a room-temperature vaporized peracetic acid (VPA) method that achieves exceptionally low chemical residuals and unsurpassed materials compatibility. The VPA technology eliminates inefficiencies associated with pre-conditioning and lengthy post-sterilization wait times. This allows REVOX Sterilization Solutions to offer manufacturers a quick-turn, off-site sterilization service or cost efficient on-site, in-line processing. The 3000L chamber, or 417L chamber, will enable in-line sterilization, allowing companies to safely and easily integrate VPA sterilization into a lean manufacturing process with no exhaust or other special infrastructure needed. A Class II implantable device has been granted FDA clearance with VPA sterilization process.
Visit Revox Sterilization Solutions at booth #102 at DeviceTalks Boston.
(See the best minds in medtech live at DeviceTalks Boston on Oct. 2.)
