Udi For Reusable Medical Devices

The udi system is intended to provide a single globally harmonized system for positive identification of medical devices.

Udi for reusable medical devices.

The udi or unique identification number europe as there is also one in the usa is one of the new things that come with the new eu mdr 2017 745 and ivdr 2017 746. For additional information on udi see the imdrf udi guidance document of december 2013. Healthcare professionals and patients will no longer have to access multiple inconsistent and incomplete sources in an attempt to identify a medical device and its key attributes. A class ii device that is required to be labeled with a udi must bear a udi as a permanent marking on the device itself if the device is a device.

In the case of reusable devices the udi is additionally required on the device itself but only two years after the date of application on the labelling for the respective class of device. The udi carrier shall be placed on the label of the device and on all higher levels of packaging and in case of reusable devices on the device itself direct marking. The ministry of food and drug safety will introduce the udi system which will manage all information from production to distribution and final use of medical devices in 2019 project has phase approach starting in 2017 device identifier production identifier 32. Readable plain text aidc technology exempt from the dm requirement o interfere with the safety performance o it is not technologically feasible 13.

Udi labelling will be required for class i devices from 26thmay 2025. Udi and gs1 gs1 is an udi issuing agency entity based on many regulations worldwide in particular us eu china south korea saudi arabia meaning that manufacturers supplying regulated medical devices to these markets can use the gs1 standards to implement the udi requirements. This element will be key for the traceability of devices in europe.