AusUDID Reference Center

Your central hub for valuable resource, guidelines, and solutions to achieve UDI compliance in Australia.

EUDAMED

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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.
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AusUDID Technical
Documentation

Download the AusUDID data dictionary, technical specifications & business rules to prepare your device data for submission to AusUDID.

AusUDID Regulation & Guidance Documents

Read the latest communications from the Therapeutic Goods Administration (TGA) regarding UDI regulations and AusUDID compliance.