Guidance on the renewal of designation and monitoring of notified bodies under Directives 90/385/EEC and 93/42/EEC to be performed in accordance with Commission Implementing Regulation (EU) 2020/666 amending Commission Implementing Regulation (EU) 920/2013

Information

Type

Guidance

Regulated products

Medical Devices

Topics

Notified Bodies

Published

May 1, 2020

Last updated

May 1, 2020

Description

This document provides guidance on the renewal and monitoring of notified bodies under EU Directives 90/385/EEC and 93/42/EEC.

Organization

Country / Region

European Union

License

Creative Commons Attribution 4.0

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