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The New European UDI System Part I


This lecture describes the key changes regarding post market surveillance and what companies should do to meet their new obligations. After the course you can take a final test to receive your certification. Enjoy!


Why take this course

The Unique Device Identification Video Course is designed to help you discover the UDI system.

What I will learn

This course will highlight the UDI system and will facilitate easier traceability of medical devices and quick identification of the specific user. This system significantly enhances the effectiveness of the post-market safety-related activities for devices and allow for better monitoring by competent authorities.

Skills I will gain

  • Discover Unique Device Identification (UDI) System
  • Explore the UDI structure and requirements
  • Learn key the timelines for registration of device data for EUDAMED
  • Understand the difference between UDI in Europe vs the USA



  • Introduction (00:02:29)
  • MDR References & UDI Purpose and Benefits (00:01:50)
  • UDI Components (00:02:42)
  • Basic UDI-DI and Unit of Use DI (00:03:26)
  • Information to be entered in EUDAMED (00:05:52)
  • MDR Timelines for registration of device data in EUDAMED (00:00:45)
  • Correlation table between MDD and MDR (00:00:50)
  • UDI in Europe vs the USA (00:07:11)

  • Final Quiz – MDR The New European UDI System (Part I)
  • Certification

Additional information

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