About this event
When developing a medical device, it is important to consider if the product will need to be sterilized or disinfected. The purpose of disinfecting or sterilizing medical devices is the removal of pathogenic microbes that could lead to contamination or infection in the user or patient. The level of disinfection or sterilization is dependent on the intended use of the medical device, and a wide range of physical and/or chemical processes can be used to sterilize them. Issues can arise in plastic components when the disinfectant chemical or sterilization process alters the molecular structure of the plastic resin, which can lead to cracking and catastrophic failure. The incident rate of plastic failure associated with sanitizing medical devices has significantly increased corresponding with efforts to eliminate disease transfer and healthcare-acquired infections (HAIs). This presentation will discuss the various sanitizing methods and their potential effect on plastic materials.
At the end of this event, attendees will have a better understanding of:
Jeff is a graduate of Carroll College and the Milwaukee School of Engineering. He is an expert in failure analysis, material identification and selection, as well as compatibility, aging, and lifetime prediction studies for thermoplastic materials.
The Madison Group is recognized as a global leader in the plastics industry. We offer a variety of customized consulting services from material selection to design verification to failure analysis and everywhere in between.
The Madison Group has been a recognized global leader providing consulting services, technical expertise and innovative technology to the plastics industry since 1993. We solve plastic problems and find economic solutions that help drive product development to yield higher quality parts.
Share this event