MEDICAL DEVICE REGISTRATION AND APPROVAL IN Qatar

MEDICAL DEVICE REGISTRATION AND APPROVAL IN Qatar

General country-specific regulatory information is provided on this page for medical device registration and approval in Qatar
Last update: December 2022

Medical Device Regulations and Classification in Qatar

Regulatory Authority: 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.

Classification System: Medical devices are classified according to EU model into risk-based Classes I, IIa, IIb, III, and IV.

Authorized Representative: A local authorized representative is required to obtain an import permit.

Additional Information: Medical devices must be authorized by one of the founding members of the Global Harmonization Task Force (GHTF) to obtain market access.

Other Middle East & North Africa Countries: Algeria,Bahrain,Egypt,Israel,Jordan,Kuwait,Lebanon,Morocco,Oman,Palestine,Tunisia,United Arabic Emirates,Yemen,Saudi Arabia

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