This Helpdesk is part of the Request for Services Chafea/2019/Health/10409 under a service contract (FWC Chafea/2017/AGRI/06 LOT 4) with the European Health and Digital Executive Agency (HaDEA) acting under the mandate from the European Commission.
The aim of the Helpdesk is to provide information concerning the Unique Device Identification (UDI) System introduced under Regulations (EU) 2017/745 on medical devices (MDR) and (EU) 2017/746 on in-vitro diagnostic medical devices (IVDR).
The information and views set out in this Helpdesk and the information provided through it are those of the author(s) and do not necessarily reflect the official opinion of the Executive Agency.
The Executive Agency does not guarantee the accuracy of the data included in this report/deliverable. Neither the Executive Agency nor any person acting on the Executive Agency’s behalf may be held responsible for the use which may be made of the information contained therein.