Swissdamed Implementation Schedule

Detailed roadmap of the Swiss medical device database from conception to full implementation

Basic work & conception
2020 - 2022
Development of the legal and technical basis for the Swiss medical device database based on EU standards.
  • Development of the legal framework (HMG/MepV)
  • Technical concept and system architecture
  • Stakeholder consultations with industry and authorities
  • Budget approval and project organisation
  • Tendering and supplier selection
Completed
Pilot Phase & Testing
2023
First test phase with selected industry partners and development of the user interface based on practical feedback.
  • Start of the first test modules (Economic Operators)
  • Feedback integration from industry partners
  • Customization of the user interface and UX
  • Initial safety and performance tests
  • Development of training materials
Completed
Rollout Phase 1
2024
Productive commissioning of the first modules and preparation of the critical UDI functionalities.
  • Economic Operators Registration (already active)
  • Authorized Representatives Module (in trial)
  • Initial training for users
  • Structure of the support system
  • Monitoring and performance optimisation
Ongoing
UDI Preparation & Certificates
2025
Intensive preparation phase for UDI implementation and activation of further critical modules.
  • Certificates Module (full implementation)
  • UDI Devices Module (Test Phase)
  • Extensive industrial training
  • API development for third-party systems
  • Compliance Checklists and Guides
In preparation
🚨 UDI Registration Mandatory
July 1, 2026
Critical milestone: From this date, all UDIs must be registered before being placed on the market. No transition period for vigilance cases!
  • Mandatory UDI registration for all new products
  • Immediate registration for vigilance notifications
  • Full system availability 24/7
  • Expanded support capabilities
  • Monitoring critical business processes
Critical Appointment
End of the transitional period
December 31, 2026
Deadline: All existing products must be registered by this date. Subsequent registration is no longer possible.
  • 100% registration of all products on the market
  • Full compliance of all economic actors
  • Completion of the migration phase
  • Start of enhanced monitoring
  • Penalty for non-compliance
Final Deadline
Full Operation & Expansions
2027 and beyond
Continuous development of the platform with new features and improved user-friendliness.
  • Full UDI search functionality
  • Advanced Vigilance Integration
  • Comprehensive API interfaces for third-party systems
  • Mobile Applications for Healthcare Providers
  • AI-based anomaly detection
  • Integration with international databases
Scheduled
Completed
Current
Critical Dates
Future