Did you know that our markers and rulers comply with the EU Declaration of Conformity for The European Medical Device Regulation (Regulation (EU) 2017/745,MDR)? We have completed the registration of our products to comply with requirements designated by the EU. Additionally, AC Wellman is a Licensed Medical Device Facility (Registration Number 1528078) under the Office of Product Evaluation and Quality for the Center for Device and Radiological Health, U.S. Food and Drug Administration.