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Australia: Unique Device Identification (UDI) Requirements: What Medical Device Manufacturers Must Know for Compliance in 2025–2030 – April/May 2025

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.

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QT ANALYSIS: The Impact of Unique Device Identification (UDI) System on Medical Device Registration – June/July 2023

QT ANALYSIS: The Impact of Unique Device Identification (UDI) System on Medical Device Registration – June/July 2023

  • 2023-06-28 09:59:48

Qualtech's big topic for this month's edition provides an overview of the Unique Device Identification (UDI) system implemented by territories serviced by Qualtech for medical devices. The UDI system aims to improve patient safety, traceability, and identification of medical devices on the market. The implementation of the UDI system offers benefits such as faster traceability, standardized post-market safety activities, and improved buying and waste disposal policies.

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