REGULATORY AUTHORITY: The Ministry of Health (MOH) oversees medical device regulation through the Jordanian Food and Drug Administration (JFDA).
CLASSIFICATION SYSTEM: Jordan accepts both the EU and FDA classification models.
TIMEFRAME: The approval process takes between four and eight months, depending on whether lab testing is required.
LICENSE VALIDITY: Licenses issued in Jordan expire when the device’s previously obtained license (from the USA, EU, or Japan) expires.
AUTHORIZED REPRESENTATIVE: A local authorized representative is required.
