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Directorate of Medical Devices Registration

  • Participating in the development of technical specifications for medical devices and spare parts to ensure the quality, safety and efficiency.
  • Classifying medical devices according to the risk posed by the device to human health as a result of its use (FDA-GHTF).
  • Studying the files of medical devices submitted for registration.
  • Conducting technical inspection of medical devices and submit technical reports.
  • Documenting all information about medical devices in the database.
  • Participating in the preparation of regulations for the importation of used medical devices.

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Application form

On line Registration