[Free Online Seminar] Electromagnetic Interference/EMC Testing of Medical Electrical Equipment
We will explain an overview of IEC 60601-1-2, including electromagnetic interference testing and changes from the 4th edition to the 4.1 edition.
[Webinar Series on Medical Device Safety Standards from the Basics 2025] Session 2: Electromagnetic Interference/EMC Testing of Medical Electrical Equipment (IEC 60601-1-2) March 25, 2025 | Free | Online Technical standards for 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 to EMC standards have been made, and the transition period to the JIS standard JIS T 0601-1-2:2023 is approaching in mid-February 2026. In this webinar, as part of the introductory series on medical device safety standards for 2025, we will provide an overview of IEC 60601-1-2, explain electromagnetic interference testing, and discuss changes from the 4th edition to the 4.1 edition. Additionally, we will introduce some testing methods for basic standards that were requested in last year's survey. For more details and to register, please follow the link below.
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We will be holding our popular series of webinars on the introduction to safety standards for medical devices again this year, with enhanced content. In its third year, we will add new themes and incorporate the latest information to clearly explain the overview of standards related to medical devices, as well as key points for safety testing and evaluation. Please also use this as internal training for personnel involved in development, regulatory affairs, and quality control at medical device manufacturers. 【7-Part Webinar Series on Understanding Safety Standards for Medical Devices 2025】 Session 1: Medical Device Regulations and Safety Standards Session 2: Electromagnetic Interference/EMC Testing for Medical Electrical Equipment (IEC 60601-1-2) Session 3: Reprocessing Validation for Medical Devices (ISO 17664) Session 4: Biocompatibility Evaluation of Breathing Gas Pathways (ISO 18562) Session 5: Brazil INMETRO Certification Session 6: Biological Evaluation (ISO 10993-1) Session 7: Chemical Characterization and Toxicity Evaluation of Medical Device Materials (ISO 10993-18) Archive Release Electrical Safety Testing for Medical Devices (ME Equipment, ME Systems) (IEC 60601-1)
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**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.
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