UDI Reference Center
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EUDAMED
Global UDI
GUDID
AusUDID
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AusUDID Reference Center
Start your compliance journey for high-risk and implanted medical devices!
The Australian Government has approved UDI amendments to the Medical Device Regulations, registered in the Federal Register of Legislation on 24 March 2025. Mandatory UDI compliance starts in July 2026 for high-risk and implanted devices, with other devices phased in according to risk class. Is your company ready to submit regulatory data to AusUDID? Innovit can help! Bookmark this page for all you need to know about AusUDID and achieving compliance.
What is
AusUDID
The Australian Unique Device Identification Database (AusUDID) is a public database that provides free access to information about medical devices supplied in Australia.
FAQ – AusUDID
Device Registration
Your answers for registering devices on the AusUDID.
AusUDID
playground
Your very own Innovit playground environment to gather, validate and test the submission of device data to AusUDID.
Coming Soon!
AusUDID Technical
Documentation
Download the AusUDID data dictionary, technical specifications & business rules to prepare your device data for submission to AusUDID.
AusUDI Regulations
Documents & Guidance
Read the latest communications from the Therapeutic Goods Administration (TGA) regarding UDI regulations and AusUDID compliance
Featured Story
AusUDID FAQ eBook
This eBook is intended to serve as a reference tool and mini-guidebook as your team navigates the complexities of AusUDID compliance.