Lebanon
General country-specific regulatory information is provided on this page. Become a LICENSALE.COM user to receive detailed device-specific compliance information for each market, free of charge, to expedite the preparation of your medical device or IVD registration application.

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.

Last updated on March 17 2015.



Interested in obtaining fast market approval for your medical device or IVD in Lebanon? REQUEST A FREE QUOTE>

For more information on registration in Lebanon, check out the following articles on our blog:
Country at a Glance: Lebanon
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