UL Japan Official site

Technical consultation meeting on medical device safety standards (60601/61010)

UL Japan

We will hold an online free technical consultation session regarding medical device safety standards (60601/61010). - "I want to confirm whether the design of the medical device under development complies with the applicable standards." - "I want to check the applicable standards for the medical device under development before requesting an evaluation." - "I want to know the latest status of the 61010-1 standard and individual standards (e.g., EN IEC 61010-2-101:2022/A11:2022, etc.)." - "I want to confirm the available services, estimated costs, required time, necessary documents/samples, and key points for component selection." - "I would like to take this opportunity to ask questions about the requirements of the 61010-1/60601-1 standards." This is recommended for medical device manufacturers who have such questions or challenges. The application deadline is until July 31, so please take advantage of this opportunity. You can check the details of the seminar by clicking the "Details & Application" button below.