LEXISNEXIS LIFE SCIENCES SOLUTIONS

Understanding UDI Series

Gain answers to your questions about Unique Device Identification (UDI). Book time with a UDI expert for in-depth Q&A plus access to a library of tutorials and reference materials

Swissdamed managed by Swissmedic

Switzerland has established its own medical device database, Swissdamed, managed by Swissmedic, to support national regulatory oversight following its transition away from direct participation in EU systems. Swissdamed is being implemented in phases, with mandatory use of the Product Module beginning July 1, 2026. This milestone will require manufacturers placing devices on the Swiss market to submit and maintain product data directly within the Swiss system, creating additional regulatory obligations for companies operating across Europe.

LexisNexis Life Sciences simplifies that complexity. We support manufacturers across the entire product lifecycle — from initial market entry and UDI data preparation to ongoing updates, change management, and post-market compliance. Our global regulatory expertise and technology-driven solutions help ensure your device data stays accurate, synchronized, and inspection-ready, so you can focus on innovation while we help safeguard compliance.

Swissdamed UDI Requirements

Timeline

Swissdamed UDI Requirements Timeline

Related Resources

BLOG
Swissmedic Launches UDI Module in swissdamed

Swissmedic Launches UDI Module in swissdamed

Voluntary submissions begin in August 2025, with mandatory registration starting July 2026. The system aligns with EUDAMED standards, compliance, and post-market surveillance.

Understanding UDI

Unique Device Identification (UDI) requirements vary by country and regulatory authority. Select a health authority below to access jurisdiction-specific guidance and resources.

USA

EUROPEAN UNION

CHINA

SOUTH KOREA

AUSTRALIA

SWITZERLAND

Need Guidance on UDI Compliance?

Understanding UDI obligations across global health authorities can be complex. Whether you are preparing for initial submission, managing product data updates, or aligning compliance across multiple markets, our regulatory experts provide practical guidance tailored to your organization’s needs.

Global UDI - Contact Us