The status of Appendixes E-I of IMDRF N48 under the EU regulatory framework for medical devices
Information
Type
Guidance
Regulated products
Medical Devices
Topics
Unique Device Identifier (UDI)
Published
June 1, 2021
Last updated
June 1, 2021
Description
This document discusses the status of IMDRF N48 Appendixes E-I under the EU regulatory framework for medical devices, focusing on the Unique Device Identifier (UDI).
Tags
Organization
Country / Region
European Union
License
Creative Commons Attribution 4.0