Medical devices Unique Device Identification (UDI)

The Australian Government is strengthening patient safety by introducing Unique Device Identification (UDI) for medical devices. UDI supports other medical device reforms designed to improve the effectiveness of the regulatory framework, including the management of post-market safety-related activities, such as recalls.

With the introduction of UDI, Australia will join a globally harmonised approach that supports more accurate tracking and tracing of medical devices (unless the device is exempt).

For UDI labelling and packaging requirements and information see Unique Device Identification (UDI) hub.

More information

Unique Device Identification (UDI) Webinar 19 - Australian UDI project update and discussing considerations and real-world benefits of adopting UDI in healthcare. 

Unique Device Identification Webinar #18 - Project checkpoint on what we know and what you can do to get involved.

Unique Device Identification Webinar #17 - Discussion on recent UDI workshop feedback and demonstration of AusUDID Pre-Production.