In an effort to educate worldwide medtech authorities about EU procedures relating to products that were certified under its Directives and Regulations, the European Commission has issued a new factsheet outlining key details on these points. The bottom line: some devices with Directives certification may be sold on the market until May of 2024, and made available until May of 2025. Find out more about how the European Commission is attempting to educate third-countries on devices and IVDs that have been CE marked under Directives from the EU in this informative Medtech Insight article.