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: January 2024

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: Unless lab tests are required, licenses do not have expiration dates.

AUTHORIZED REPRESENTATIVE: A local license holder, which is also appointed as an importer, is required.

Other Middle East & North Africa Countries: Algeria,Bahrain, Egypt,Israel,Kuwait,Lebanon,Morocco,Oman,Palestine,Qatar,Saudi Arabia,Tunisia,United Arabic Emirates ,Yemen

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