EUDAMED Production v2.22.0: What Manufacturers Need to Know
EUDAMED Production v2.22.0 introduces EMDN versioning, improved traceability, and DTX updates. Learn what this means for manufacturers.
European Commission Confirms Functionality of Key EUDAMED Electronic Systems: What This Means for Medical Device Manufacturers
The European Commission has confirmed that four core EUDAMED electronic systems—economic operator registration, UDI and device registration, notified bodies and certificates, and market surveillance—are fully functional. This triggers mandatory transition timelines and introduces significant new obligations for medical device manufacturers.