Medical Device Registration and Approval in Jordan
General country-specific regulatory information is provided on this page for medical device registration and approval in Jordan.
Last updated on November 24th, 2021.
Medical Device Regulations and Classification in Jordan
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.
Please fill out your contact information so we can better assist you.
* Note: If you use your general ISP e-mail address, such as gmail, yahoo etc. your LinkedIn profile address is required to process your request.