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.
Tags
Organization
Country / Region
European Union
License
Creative Commons Attribution 4.0