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).

Organization

Country / Region

European Union

License

Creative Commons Attribution 4.0

Feedback

Suggest an improvement to this page

Actions

Social networks

Embed