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Medical Device Registration and Approval in Lebanon
General country-specific regulatory information is provided on this page for medical device registration and approval in Lebanon.
Last updated on April 12th, 2022.
Medical Device Regulations and Classification in Lebanon
REGULATORY AUTHORITY: The two bodies regulating medical device registration in Lebanon are The Drug Import and Export Department and The Sanitary Engineering Service, which both act under the Ministry of Public Health.
CLASSIFICATION SYSTEM: The Lebanese authorities accept all classification systems.
TIMEFRAME: Medical device registration in Lebanon requires a period of three months.
LICENSE VALIDITY: The registration process is an import permit and must be performed with every shipment. Only implantable devices are regulated at the moment.
AUTHORIZED REPRESENTATIVE: A local representative is required.
For detailed device-specific compliance information for each market, including Lebanon, to expedite the preparation of your medical device or IVD registration application.
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