The cleaning, disinfection, and sterilization of medical devices are critical processes that ensure patient safety and device efficacy. This presentation will focus on the latest updates to reprocessing guidance documents AAMI TIR 12 and TIR30 (ST98), which provide detailed recommendations for these procedures.
Viewers will gain an understanding of the new revisions and how they impact the reprocessing of medical devices. The session will cover the comprehensive steps involved in cleaning, disinfection, and sterilization, including pre-cleaning, manual and automated cleaning, disinfection methods, and sterilization techniques. Emphasis will be placed on the importance of validating these processes to ensure their effectiveness.
Practical examples and case studies will illustrate how the updated guidance can be implemented in various healthcare settings, addressing common challenges such as handling complex devices and ensuring compatibility with different materials. By the end of this presentation, participants will be equipped with the knowledge to apply the updated AAMI TIR 12 and TIR30 (ST98) guidance in their facilities, ensuring compliance with regulatory standards and enhancing patient safety.