Difference between Medical Device, Accessory, Spare Part, and Consumable according to MDR The European Medical Device Regulation (MDR 2017/745) provides clear definitions and requirements for various categories of products in…
Europe IT Consulting GmbH is offering a webinar on the subject of UDI and EUDAMED on Tuesday, April 9th, 2019, 10:00 a.m. - 11:00 a.m. <! - more -> <…
The FDA has laid the foundation with its UDI system and the GUDID database. Many countries are not yet ready to allow medical device manufacturers to automatically upload their data.…
The 24th HIBC User Day was very informative regarding the currently dominating topic "Unique Device Identification". Following the motto "Marking, registering, using UDI", the most important key points were again…