Are you ready for the Unique Device Identification (UDI) System requirement under the EU Medical Device Regulations 2017/745 and 2017/746 regulation – Effective May 2020?

Are you ready for the Unique Device Identification (UDI) System requirement under the EU Medical Device Regulations 2017/745 and 2017/746 regulation – Effective May 2020?

The European Medical Device Regulations for Unique Device Identification (UDI) will be effective May 2020, this mandates that any company supplying Medical Devices in the European Union are legally obliged to comply. Are you compliant?

May 2020, a Unique Device Identification (UDI) must be assigned by the manufacturer to every medical device, and every time there is a change in the product the manufacturer must evaluate the UDI. Are you ready for May 2020?