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UDI: Information for sponsors and manufacturers
Information to support sponsors and manufacturers understand and apply Unique Device Identification (UDI) requirements to their medical devices.
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Unique Device Identification (UDI) is a global harmonised identifier that can support the tracking and tracing of medical devices.
If UDI is widely adopted, it can enable faster identification of devices, improved data quality, reductions in data errors and inconsistencies, support anti-counterfeiting measures, and enable consistency in data capture and greater automation.
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PageUnderstand and apply the requirements to your medical devices.
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PageUnderstand and apply the UDI labelling and packaging requirements to your medical devices.
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PageUnderstand how UDI will integrate with existing TGA requirements.
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PageUnderstand what the Australian UDI database is and how to use it.
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Post: | Devices Reforms Taskforce |