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European Ombudsman
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Reply by the European Commission to a proposal for a solution from the European Ombudsman on its decision revise the risk classification of devices involving brain stimulation under rules governing products without an intended medical purpose in the context of the EU Medical Devices Regulation

Correspondence - Date Friday | 08 March 2024
Case 1157/2023/VB - Opened on Friday | 07 July 2023 - Decision on Friday | 07 July 2023 - Country France

  • Complaint submitted
    22/06/2023
  • Analysis of the complaint
    23/06/2023
  • Inquiry outcome
    07/07/2023

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