A series of consultations have informed the planning and design of Unique Device Identification (UDI) implementation in Australia. Consultations have included public consultation papers, stakeholder workshops, webinars, targeted discussions and technical, regulatory and consumer working groups.
Consultation papers via the links below:
- UDI Consultation Paper 1 (2019) - Proposal to introduce a Unique Device Identification (UDI) system for medical devices in Australia
- UDI Consultation Paper 2 (2020) - Exploring options for the introduction of an Australian Unique Device Identification (UDI) System
- UDI Consultation Paper 3 (2022) - Detailed considerations for implementing the proposed Australian medical device UDI regulatory framework