Get your medical devices registered and approved to ensure legal compliance and safe use in your clinic or facility Why Medical
MOH Registration and Approvals for Medical Equipment in the UAE
Get your medical devices registered and approved to ensure legal compliance and safe use in your clinic or facility
Why Medical Equipment Needs MOH Approval
Before any medical device can be sold, distributed, or used in a healthcare setting in the UAE, it must be approved by the Ministry of Health and Prevention (MOH). This applies to a wide range of equipment, from diagnostic machines and surgical tools to dental chairs, dermatology lasers, and even basic monitoring devices.
The goal of this process is to ensure that all medical equipment used in the UAE meets local safety, quality, and performance standards. For healthcare providers, this approval is not optional. Using or importing unregistered equipment can result in penalties, license issues
Who Needs This Service
This service is essential for any healthcare supplier engaged in providing equipment to clinics, pharmacies, optical centers, hospitals, or laboratories.
How ProHealth Helps with MOH Equipment Registration
ProHealth works closely with approved local agents and MOH portals to register your medical devices correctly. We assist with the full documentation process, including:
- Verifying the manufacturer’s certificates and product data
- Classifying the device according to MOH categories
- Coordinating with local representatives for registration submissions
- Tracking the approval status and managing any required clarifications
If the equipment you want to use is not yet registered, we help you explore alternate options or guide you through the official import approval process for special cases.
Equipment Compliance and Approvals
Getting MOH approval is not just about having the right product, it’s also a critical step in getting your clinic or facility licensed.
The Ministry of Health (MOH) registration process can be intricate and time-consuming, particularly for healthcare businesses unfamiliar with the requirements. By partnering with the ProHealth team, you can be assured that the registration of your healthcare products with the MOH will be managed with expertise and efficiency.
Simplifying a Complex Process
The equipment registration process involves multiple stages, document preparation, submission and follow-ups. Our team manages all of this on your behalf, providing regular updates and handling any queries directly with the health authority.
Start With Confidence
If you are setting up a healthcare business and to register the products with MOH., ProHealth is here to make sure everything is managed and MOH-compliant. Get in touch with us today to discuss your requirements, and we will guide you through the approval process from start to finish.
