The EUDAMED UDI/Devices module becomes mandatory on 28 May 2026. From this date, manufacturers must register all new devices before placing them on the EU market.
Need a hand navigating the system, particularly the UDI module?
Advena is offering live, interactive virtual support tailored specifically to the EUDAMED UDI Module. In a face-to-face virtual consultation, a real expert will sit down with your team to guide you through the system step-by-step. We’ll make sure your access permissions are set up perfectly and walk through the device registration process together.
What is included:
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A one-hour, fully interactive virtual call with an experienced consultant and your team.
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A walkthrough of your user access permissions to ensure the correct setup (certain permissions are strictly required for the UDI module).
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Help sorting out user access requests (please ensure other admin users are on standby in case access needs to be granted during our call).
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Real-time Basic UDI registration using one of your actual devices as a live example.
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Step-by-step guidance through UDI-DI and device registration under the Basic UDI.
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Open Q&A throughout the session so you can ask questions as we go.
What you’ll need before the session:
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An active EUDAMED login (Actor registration must already be complete).
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All registered users present on the call to review their permissions.
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At least one device to use as our live registration example.
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Your Declaration of Conformity, IFU, Basic UDI, and UDI-DI number to hand.
Who needs to attend:
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Your team: We highly recommend having more than two EUDAMED users on the call, just in case any access permissions need to be changed on the spot.
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Advena: Your friendly, EUDAMED-experienced consultant, ready to help you build confidence in navigating the system.
Contact Us
For further information and personalised guidance, please feel free to reach out to Advena via either our website contact page, www.advenamedical.com, email (info@advenamedical.com) or phone (01926 800153) to start a conversation today.
