MEDICAL DEVICE REGISTRATION AND APPROVAL IN Lebanon

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 update: December 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.

 

JUST SAY WHEN!

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 country-specific registration process in this country or any of the other 140+ countries available for you through the Arazy Group Medtech registration platform. You can start your product registration right now!

Ready to Get Started?