The Therapeutic Goods Administration (TGA) maintains the Australian Unique Device Identification Database (AusUDID). The AusUDID stores Unique Device Identification (UDI) records for medical devices supplied in Australia.
About the AusUDID
Learn about the AusUDID and how to use the database to comply with UDI requirements.
Accessing the AusUDID
Learn about the AusUDID and how to use the database to comply with UDI requirements.
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PageUnderstand the roles in the AusUDID and what each role can do.
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User guideLearn how to access the AusUDID Production and Pre-Production environments.
Submitting and managing UDI records in the AusUDID
Learn about the different ways to submit UDI records to the AusUDID. Understand how to maintain UDI records and use the different functionality in the database.
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PageLearn about the different ways you can submit UDI records to the AusUDID.
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PageLearn best practice tips to help you create accurate, complete and compliant UDI records.
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User guideLearn how to create and manage UDI records in the AusUDID online portal.
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User guideLearn how to prepare and submit up to 200 UDI records at once using the Australian UDI Bulk Upload Template.
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PageResources and technical documents for Machine to Machine (M2M) HL7 SPL users in the Australian Unique Device Identification Database (AusUDID).
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PageLearn how to electronically submit UDI records using GS1’s National Product Catalogue (NPC).
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User guideLearn how to manage UDI records when a device is supplied by more than one sponsor.
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User guideLearn how to search, view and download UDI records in the AusUDID.
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PageFind solutions to common issues when accessing or submitting UDI records to the AusUDID.
AusUDID concepts
Understand key concepts that apply to creating and managing UDI records in the AusUDID.
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PageUnderstand key concepts that apply to creating and managing UDI records in the AusUDID.
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