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: Medical devices in Qatar are managed by the Ministry of Economy and Commerce (MEC). Currently medical devices do not require registration, but they do require an import permit, which must be obtained by a local authorized representative.
Medical devices are classified according to EU model into risk-based Classes I, IIa, IIb, III, and IV.
A local authorized representative is required to obtain an import permit.
Medical devices must be authorized by one of the founding members of the Global Harmonization Task Force (GHTF) to obtain market access.
Last updated on October 22, 2018.
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