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Master Global UDI Compliance — Get Our Free Guides
Three complementary resources for manufacturers managing UDI compliance across EUDAMED, GUDID and other databases: the global Reference Guide, our EUDAMED White Paper, and a practical Quick Guide. Fill in the form to access all three.
One platform · every major UDI database
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INSIDE THE PACK
What You Will Find in Our Resources
White Paper — From Filing to Active Management
Quick Guide — Master EUDAMED Compliance
OUTCOMES
What You Will Learn
Map every requirement once
Compare data elements across 7 databases instead of researching each one separately.
Anticipate global deadlines
A single calendar of registration and reporting milestones, by jurisdiction.
Prepare for inspections
Know what auditors look for and structure your evidence accordingly.
Manage data over time
Shift from one-off filing to continuous, audit-proof data management.
WHY ACKOMAS
Why Trust Ackomas
Regulatory specialists
Built by UDI and regulatory data experts across EUDAMED, GUDID, Swissdamed and more — not generalists.
Trusted by manufacturers
Medical device and IVD companies rely on Ackomas across the EU and beyond.
Always up to date
Guidance maintained as databases, deadlines and rules evolve.
See how ACKOMAS keeps your UDI data compliant across every database
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