The introduction of the Unique Device Identifier (UDI) system represented a milestone in the regulation of medical devices on the European market. The system, defined in Regulation (EU) No 2017/745 of the European Parliament and of the Council on Medical
Unique Device Identification (UDI) is an identification system that has become a key element in the regulation of medical devices within the European Union. The system was introduced to increase the level of patient safety and the effectiveness of medical
EUDAMED (European Database on Medical Devices) and UDI (Unique Device Identification) are integral components of the European Union’s regulatory framework for medical devices. Here’s a brief overview of each: Both EUDAMED and UDI represent importa
EUDAMED (European Database on Medical Devices) and UDI (Unique Device Identification) are integral components of the European Union’s regulatory framework for medical devices. Here’s a brief overview of each: Both EUDAMED and UDI represent important steps towards greater transparency and
