White Paper: Insights into Testing and Certifying Medical Devices for Global Access to IEC 60601-1-2


The medical industry is rapidly adopting new technology, which enables better communication and performance of products and systems to improve patient safety.

Stringent regional approval procedures for electrical medical devices typically require independent third-party testing by an approved laboratory to the IEC 60601 standard. IEC 60601-1-2 for Medical Electrical equipment is now in its 4th edition and supersedes EN 60601-1-2:2007. This is a major update with significant changes and therefore compliance implications.

As the first ever NRTL, and one of the world's largest and most reliable medical device testing laboratories, we can guide you through the process. You can access the information you need to start your testing by following the steps below.

  1. Click  below to download our Our FREE white paper to learn more about certifying medical electrical devices to the IEC 60601-1-2 standard. DOWNLOAD FREE IEC 60601-1-2 WHITE PAPER

If you have questions, or if you need more information, email marketing@metlabs.com or click HERE.

 

Eurofins E&E North America - White Paper - 4th Edition of 60601-1-2 - December 2020_Page_1