The MDD to MDR transition period concluded with the official MDR date of application on May 26, 2021. During this transition period, Merit’s global team has worked on the comprehensive implementation of the European Union’s new Medical Device Regulation (MDR).

After months of diligent work, Merit received our first MDR Notified Body certificate of compliance for our complete line of PC and COP syringes. Merit’s global cross-functional team continues to work on MDR compliance for our complete product catalog, now that MDR is required for CE marked products.

Secure your supply chain and MDR regulatory approval at the same time with Merit’s American made and MDR certified syringes.