Overview
This video explains why the May 28 and November 28 EUDAMED milestones matter and why medical device manufacturers need coordinated data, registration, process ownership, and regulatory execution before deadlines create avoidable risk.
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USDM video
EUDAMED Has Landed: The Two Big Deadlines, May 28 vs. Nov. 28
Watch a short overview of the two major EUDAMED deadlines and what medical device teams should understand as mandatory use approaches.
1:35 May 15, 2026
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Watch the short overview, then use the links below to keep moving: explore the related capability, browse more resources, or start a conversation with USDM.
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What to take from it
1
Understand why the May 28 and November 28 EUDAMED dates are important planning milestones for medical device manufacturers.
2
Learn why readiness depends on device data quality, clear regulatory ownership, submission workflows, and repeatable maintenance processes.
3
Identify practical next steps for reducing deadline risk, improving traceability, and preparing teams for ongoing EUDAMED obligations.
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EUDAMED Readiness
Learn how USDM helps medical device manufacturers prepare for EU MDR/IVDR, UDI, and EUDAMED readiness requirements.
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Explore USDM guidance for regulated life sciences teams managing changing compliance, quality, and submission requirements.
Learn MoreTalk with USDM
Start a conversation about EUDAMED readiness, UDI data, EU MDR/IVDR compliance, or regulatory execution planning.
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