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: January 2024

Medical Device Regulations and Classification in Qatar

REGULATORY AUTHORITY: The Ministry of Public Health is responsible for regulating medical devices in Qatar.

CLASSIFICATION SYSTEM: Qatar accepts both FDA and CE classifications, they consist with the EU classification system (I, IIa, IIb, III).

LICENSE VALIDITY: Until the expiry date of the supporting certificate (CE/FDA).

AUTHORIZED REPRESENTATIVE: A local authorized representative is required.

ADDITIONAL INFORMATION: Currently, only implantable devices require registration in Qatar. The information above is related to this type of device.

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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