IEC 60601-2-10 Edition 2.2 (2023) | FAQ Paper

Manufacturers of muscle stimulation devices face a critical update with the publication of IEC 60601-2-10, Edition 2.2 (2023). While this new edition does not introduce technical changes from Edition 2.1 (2016), compliance requires updated test reports aligning with the latest standards, including IEC 60601-1, Edition 3.2, and the updated EMC requirements per IEC 60601-1-2:2014/AMD1:2020. To ensure a smooth transition, Intertek's medical device experts have created a comprehensive Q&A document clarifying these essential updates and regulatory implications. Register below to download your copy and confidently navigate this important regulatory update.