UNDERSTANDING THE IMPACT OF UDI REQUIREMENTS FOR MEDICAL DEVICE MANUFACTURERS IN AUSTRALIA

Australia, 20 FEB 2026 – The Australian government has taken a significant step in enhancing patient safety with the introduction of Unique Device Identification (UDI) requirements for medical devices. Effective from February 2026, this initiative, backed by the Therapeutic Goods Administration (TGA), aims to improve traceability, support post-market surveillance, and make regulatory actions like recalls […]