Regulations

What is a Medical Device Marketing Authorization (MDMA)?

A Medical Device Marketing Authorization (MDMA) is an approval issued by the Saudi Food and Drug Authority (SFDA) for a medical device before it is placed on the Saudi market, confirming that the product meets SFDA requirements.

Why it matters to buyers

When purchasing a medical device, hospitals usually ask for evidence that the product may be marketed in Saudi Arabia. The marketing authorization is one of the key documents for this.

How to check it

The SFDA publishes its official services and information on its website. You can request the regulatory documents for each item together with the quotation.

For current requirements, always refer to the SFDA's official source.

Request a quotation

Send the product list, specifications and quantities, and our Riyadh team will reply with availability and terms.