The registration of medical equipment in the UAE is a mandatory regulatory process overseen by the Ministry of Health and Prevention (MOHAP). This service is critical for manufacturers and distributors who intend to import, market, or distribute medical devices within the UAE.

The process begins with the registration of the Marketing Authorization Holder (MAH) or the local medical warehouse, followed by a comprehensive technical evaluation of the device itself. Devices are classified into four categories based on their risk level.

Forin Plus provides expert guidance through the MOHAP e-services portal, assisting in the preparation of the technical dossier, ensuring all labeling requirements meet UAE standards, and managing the submission process to avoid costly delays.