Reed Tech Insights Series – EU UDI
This series is designed to provide a ‘deep-dive’ into understanding and preparing medical device product data for EU UDI submission. Learn more about the data attributes, regulatory, legislation, and distinct differences between FDA GUDID and EU EUDAMED.
Understanding Unique Device Identification Basics
Understanding Company ID – DUNS & SRN
Understanding Issuing Entities
What is BUDI-DI and How is it used in EU UDI Requirements?
Understanding Product Approval Cert