MOH Classification of Products
Classify your medical products correctly the first time. We determine and confirm the right MOHAP category for your product.
Overview
Before any medical device, equipment, or healthcare product can be registered and sold in the UAE, it must be correctly classified under the Ministry of Health and Prevention (MOHAP) framework. Classification determines the registration pathway, the documentation required, and the regulatory controls that apply, and an incorrect classification can derail the entire registration process.
Bacora determines the correct classification for your product and prepares the classification request to MOHAP standards. We assess the product’s intended use, risk class, and regulatory category, then submit and follow up so you start the registration journey on the right footing, avoiding the costly delays that come from getting classification wrong.
What Bacora Handles
- Assess the product’s intended use, composition, and risk profile
- Determine the correct MOHAP classification and registration pathway
- Confirm the device or product risk class against UAE regulations
- Prepare the classification request with all supporting documentation
- Submit the request to MOHAP and respond to any queries
- Confirm the classification outcome and advise on the next steps
How We Work, Step by Step
A clear, structured process from first contact to final delivery.
Product Assessment
We review your product’s intended use, technical details, and risk profile in depth.
Classification Determination
We determine the correct MOHAP category and the registration route it implies.
Submission
We prepare the classification request with full documentation and submit it to MOHAP.
Confirmation
We obtain the classification outcome and guide you into the registration process.
Frequently Asked Questions
Why does classification matter before registration?
Classification defines the entire registration pathway, which documents you need, which controls apply, and how the product is reviewed. Getting it wrong means preparing the wrong file and facing rejections and delays. Correct classification up front saves significant time and cost.
What types of products need MOHAP classification?
Medical devices, equipment, in-vitro diagnostics, and a range of other healthcare products fall under MOHAP classification and registration. The right category depends on the product’s intended use and risk. We confirm whether and how your specific product is classified.
How is risk class determined?
Risk class is based on factors such as how invasive the device is, how long it contacts the body, and the consequences of failure. Higher risk classes face stricter requirements. We assess your product against the criteria and assign the correct class in the classification request.
Can you handle classification and registration together?
Yes. Classification is the first step and registration follows directly from it. We manage both as a continuous process, so once your product is correctly classified we move straight into preparing and submitting the registration file.
Ready to Get Started?
Book a free consultation. We will review your situation and tell you exactly what you need and how long it will take.
