Guidance on appropriate surveillance regarding the transitional provisions under Article 120 of the MDR with regard to devices covered by certificates according to the MDD or the AIMDD

Information

Type

Guidance

Regulated products

Medical Devices

Topics

Notified Bodies

Published

May 1, 2024

Last updated

May 1, 2024

Description

Guidance on surveillance for devices covered by MDD or AIMDD certificates under Article 120 of the MDR.

Organization

Country / Region

European Union

License

Creative Commons Attribution 4.0

Feedback

Suggest an improvement to this page

Actions

Social networks

Embed