TGA Introduces Australia's UDI System with Phased Implementation Through 2029
The TGA has introduced Australia's Unique Device Identification (UDI) system with a phased implementation through 2029. Learn about the implementation timeline, AusUDID requirements, and what medical device and IVD manufacturers need to prepare.
Australia Updates Guidance on UDI Compliance Timeframes for Medical Devices
The TGA has updated its guidance on UDI compliance timeframes for medical devices in Australia, including clarifications on legacy devices, EU MDR transitions, consignment stock, and Surgical Loan Kits.
CMS Proposes New UDI Measure Under Medicare Interoperability Program
CMS proposes a new UDI measure requiring hospitals to attest use of EHR systems to capture implantable device UDIs, reinforcing FDA UDI system adoption.
ANVISA Publishes Draft Normative Instruction on UDI Data Transmission and SIUD Management
ANVISA publishes draft rules on UDI data transmission and SIUD management in Brazil. Learn how the new requirements impact medical device manufacturers.