Webinar – How to Ensure EUDAMED Compliance for Legacy Devices | Ackomas
The countdown is on: starting January 2026, all medical devices must be registered in EUDAMED. For Legacy Devices—those still certified under MDD/IVDD—this creates a strategic and operational compliance challenge. In 30 minutes, discover how to: – Identify which devices need registration – Choose the correct coding (Basic UDI-DI, UDI-DI…) – Anticipate workload and avoid non-compliance risks – Use automation to simplify EUDAMED submission Join experts from Ackomas and Efor for an actionable session to secure your compliance plan for 2025.
Reserve your seat today
Join our 30-minute expert webinar and avoid the most common pitfalls of EUDAMED compliance. Designed for RA, QA and IT teams.
EUDAMED becomes mandatory in 2026
From January 1st, non-registered devices will no longer be marketable in the EU. Legacy compliance is urgent.
Manual methods are no longer viable
Excel tracking is error-prone and slow. Regulatory data deserves automation and control.
Regulatory risk is real
Missed registration deadlines can lead to blocked market access, fines, or product withdrawals.
What You’ll Learn in This Webinar
Clarify device registration obligations
Understand exactly which Legacy Devices require EUDAMED registration.
Choose the right codes
Learn how to apply Basic UDI-DI, UDI-DI, and other identifiers.
Minimize workload and delays
Anticipate the workload and avoid rushed or late declarations.
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