VH2O2 has been a common sterilization option for reusable devices for many years. Interest has increased for single-use device. The publication of ISO 22441:2022 and its recognition by the US FDA — coupled with the FDA’s 2024 reclassification of VH2O2 sterilization as an Established Category A process in 2024 — support this modality of sterilization. Each sterilization modality has its limitations, and there is not one modality that works for all the medical products. This session will provide essential knowledge for further considerations.
Attend this webinar and learn:
- Recent regulatory changes and regulatory consideration
- Options for implementation
- What to consider when choosing your sterilization method
