Open only to full-conference registrants with a badge. Collect your ticket at the Solutions Circle check-in desk at least 15 min before session start. First-come, first-served seating; standby tickets issued when full. Seats held for 3 minutes after start time.
Description: Regulation (EU) 2023/1542 adds a lifecycle approach to the regulation of batteries, including conformity assessment and CE-marking. It also extends to batteries incorporated in appliances - which may very well be medical devices. In this solution circle I would like to discuss current impact for medical device manufacturers that have devices that are batteries or incorporate batteries with respect to regulatory strategy, necessary documentation and labeling. We will take into account current developments and existing experiences.
Learning Objectives:
Upon completion, participants will be able to identify the impact of the EU Battery Regulation on their medical device.
Upon completion, participants will be up to date on the current implementation status of the EU Battery Regulation.
Upon completion, participants will be able to draw from experience of peers and best practice solutions to become and stay compliant with the EU Battery Regulation.
