Australia: Unique Device Identification (UDI) Requirements: What Medical Device Manufacturers Must Know for Compliance in 2025–2030 – April/May 2025
- 2025-04-24 06:13:27
Australia’s implementation of the Unique Device Identification (UDI) system marks a major advancement in medical device traceability and regulatory oversight. This article provides medical device manufacturers with essential guidance on the TGA’s UDI requirements, timelines, and compliance obligations from 2025 through 2030. It also outlines key roles, exemptions, and actionable strategies to support successful market access and patient safety.
More