Guidance on significant changes regarding the transitional provision under Article 120 of the MDR with regard to devices covered by certificates according to MDD or AIMDD

Information

Type

Guidance

Regulated products

Medical Devices

Topics

Notified Bodies

Published

September 1, 2023

Last updated

September 1, 2023

Description

Document provides guidance on significant changes related to transitional provision under Article 120 of the MDR for devices covered by MDD or AIMDD certificates, focusing on Notified Bodies.

Organization

Country / Region

European Union

License

Creative Commons Attribution 4.0

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