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: The Ministry of Health (MOH) oversees medical device regulation through the Jordanian Food and Drug Administration (JFDA).
Jordan accepts both the EU and FDA classification models.
The approval process takes between four and eight months, depending on whether lab testing is required.
Licenses issued in Jordan expire when the device’s previously obtained license (from the USA, EU, or Japan) expires.
A local authorized representative is required.
Last updated on March 17 2015.
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For more information on registration in Jordan, check out the following articles on our blog:
Country at a Glance: Jordan