Medical device registration in United Arabian Emirates

United Arab Emirates
Medical Devices manufacturers that want sold their devices in United Emirates market are subject to registration.
Manufacturers must submit the registration application to the DCD
Device classification is based on a four-tier system (Class I, II, III, and IV).
Maytal experts, together with their partners located into the UAE, can:
  • prepare medical device submission dossier
  • manage the relationships with the Authority, during the review process
  • Supply local representation service, necessary for foreign manufacturers.