Just recently convened, last week’s 8th Annual gathering of Europe’s operating room nurses  – known as EORNA 2017 –  included in the program a discussion of the new European Medical Devices Regulations as they pertain to reprocessed and remanufactured single-use devices (SUDs).  AMDR’s President, Dan Vukelich, presented to EORNA attendees the latest data on the safety, savings and sustainability that SUD remanufacturing offers. During the convention, the finalized text for the new EU medical device regulations was published in the Official Journal of the European Union, further bringing into focus the future of SUD remanufacturing for Europe’s healthcare consumers.