General country-specific regulatory information is provided on this page for medical device registration and approval in Lebanon.
We review our Regulatory Information frequently; please check back often for updates
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.
Did you know you can onboard your medical device or IVD compliance information to our system in less than 15 minutes?
And, in less than a minute, you can start your device-specific registration application and a complete county-specific registration process in this country or any of the other 140+ countries available for you through the Arazy Group Medtech registration platform.
