What Every Biomedical Tech Should Know About Tabletop Autoclaves
Why proper classification, maintenance, and monitoring of tabletop autoclaves matter more than you think.
Why proper classification, maintenance, and monitoring of tabletop autoclaves matter more than you think.
AAMI is accepting nominations for its 2025 awards, celebrating excellence and innovation in health technology.
The FDA announced that it considers vaporized hydrogen peroxide (VHP) to be an established method of sterilization for medical devices.
Why proper classification, maintenance, and monitoring of tabletop autoclaves matter more than you think.
The Environmental Protection Agency has announced plans to propose an air pollution rule to address emissions of ethylene oxide at commercial sterilizers.
Read MoreThe KILMER Conference prompted conversations about the need to connect the dots for sterility assurance through the product lifecycle.
Read MoreThe FDA is considering a master file pilot program for premarket approval holders whose approved devices are sterilized using radiation.
Read MoreThe improved guidance document addresses new technologies as well as concerns about medical device cleanliness and patient safety.
Read MoreA VA Medical center briefly halted medical procedures this year after discovering concerns involving the reprocessing of reusable medical equipment.
Read MoreFollowing a unique collaboration between medical industry leaders, the Association for the Advancement of Medical Instrumentation (AAMI) has published the latest installment in a growing collection of best practices and strategies for the sterilization of medical devices and tools.
Read MoreThe new integration enables biomedical engineers to respond more quickly to device safety issues in an era of COVID-19.