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[Webinar Series on Medical Device Safety Standards from the Basics 2025] Session 2: Electromagnetic Interference/EMC Testing for Medical Electrical Equipment (IEC 60601-1-2)
The technical standards targeting medical devices are complex and varied, including the IEC 60601-1 series and individual standards from the IEC 60601-2 series. Additionally, in recent years, revisions have been made to the EMC standards. In this webinar, as part of the introductory series on safety standards for medical devices in 2025, we will provide an overview of IEC 60601-1-2, explain electromagnetic interference testing, and discuss the changes from the 4th edition to the 4.1 edition. We will also introduce some testing methods for basic standards that were requested in last year's survey.
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[Webinar Series on Medical Device Safety Standards from the Basics 2025] Session 1: Medical Device Regulations and Safety Standards
We will be holding our popular webinar series on the introduction to safety standards for medical devices again this year, enhancing the content as always. In its third year, this time we will add new themes and incorporate the latest information, providing clear explanations of the overview of standards related to medical devices, as well as safety testing and evaluation points. We encourage you to use this as internal training for those involved in development, regulatory affairs, and quality control at medical device manufacturers. This webinar serves as an introduction to the "Webinar Series on Understanding Safety Standards for Medical Devices from the Basics," where we will introduce the regulations and standards for testing and evaluation related to safety for medical devices in major countries. We will also delve into the standards concerning usability and cybersecurity that will be applicable in Japan in 2024. We hope this will help you understand and prepare the necessary items for testing and evaluation in advance, thereby reducing the burden of applications as much as possible.
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[Medical Device Safety Standards Introductory Seminar Series 2024] Session 3: Biocompatibility Evaluation of Respiratory Gas Pathways (ISO 18562)
ISO 18562 requires testing and evaluation of particulate matter, volatile organic solvents, and condensation that occurs in medical devices with respiratory gas pathways, playing a crucial role in ensuring safe use. This seminar will provide a simple introduction to the testing and evaluation content of ISO 18562. It will be beneficial not only for manufacturers of medical devices that already have respiratory gas pathways but also for those planning to develop such devices in the future. Additionally, there was a revision of the ISO 18562 standard in March of this year, and we will also introduce the key points of that revision. You can check the details of the seminar by clicking the "Details & Registration" button below.
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[Medical Device Safety Standards Introductory Seminar 2024] Session 2: Electromagnetic Interference/EMC Testing of Medical Electrical Equipment (IEC 60601-1-2)
The technical standards targeting medical devices are complex and varied, including the IEC 60601-1 series and individual standards from the IEC 60601-2 series. In recent years, revisions have been made to EMC standards, and the transition period to the JIS standard JIS T 0601-1-2:2023, issued in February 2023, is approaching in mid-February 2026. In this seminar, as part of the introductory series on safety standards for medical devices in 2024, we will not only provide an overview of IEC 60601-1-2 and an explanation of electromagnetic interference testing but also discuss the changes from the 4th edition to the 4.1 edition of IEC 60601-1-2 in line with JIS T 0601-1-2:2023. You can check the details of the seminar by clicking the "Details & Registration" button below.
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Technical consultation meeting on medical device safety standards (60601/61010)
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.

AboutUL Japan
~ Working for a safer world since 1894 / Aiming for a safer world ~
**Overview of UL** UL addresses challenges in safety, security, and sustainability through the application of science, contributing to the creation of a better world. By enabling the safe introduction of advanced products and technologies, UL enhances trust. The staff at UL share a passion for making the world a safer place. From third-party research to standards development, testing, certification, and the provision of analysis/digital solutions, UL aims to build a healthier global society through its operations. The trust in UL supports smart decisions made by businesses, manufacturers, government authorities, regulatory agencies, and individuals. For more details, please refer to the website (UL.com). **Overview of UL Japan, Inc.** UL Japan, Inc. was established in 2003 as the Japanese subsidiary of UL, a global third-party safety science organization. Currently, leveraging UL's global network, it provides conformity assessment services for certification marks required for products in the North American UL mark, as well as safety and EMC certification PSE and S marks based on Japan's Electrical Appliance and Material Safety Law, and certification marks needed for the European and Chinese markets.