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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.

7 UDI databases mapped side by side
160+ data elements, one reference
Inspection-ready fact sheets and timelines

One platform · every major UDI database

EUDAMED
GUDID
Swissdamed
SFDA
MHRA
TGA
NMPA

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INSIDE THE PACK

What You Will Find in Our Resources

White Paper — From Filing to Active Management

Move from one-off registration to active data management
Lifecycle compliance strategy for EUDAMED
Common pitfalls and how to avoid them

Quick Guide — Master EUDAMED Compliance

Step-by-step EUDAMED onboarding
Key deadlines at a glance
Available in English, French, Italian, German

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.

Ready to talk?

See how ACKOMAS keeps your UDI data compliant across every database

Book a free diagnostic. Tell us your scope and our RA/QA experts get back within 48h with the right next step.

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