Medical Device Registration 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: The Lebanese authorities accept all classification systems. The type of product dictates the procedure it must undergo before receiving marketing authorization.
The process must be carried out by a local representative.
Timeframe of registration: Medical device registration in Lebanon requires a period of three months.
Length of license: The registration process is an import permit and must be performed with every shipment.
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