MEDICAL DEVICE REGISTRATION AND APPROVAL IN Jordan

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 update: December 2022

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.

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