Qatar Medical Device Registration

Regulatory Authority

Ministry of Public Health

Link for Regulatory Authority

https://www.moph.gov.qa/english/Pages/default.aspx

Local Regulation

Classification of Medical Devices

Class I, IIa, IIb, III and IV

Listing or Registration Requirements

No registration required.

Import license should be obtained by AR. Registration in Qatar requires prior approval in one of the following GHTF markets: Australia, Canada, Europe, Japan, or the USA.
Generally, medical device or IVD classification in the reference market will determine the class of device.

Documents Required for Qatar Medical Device Registration

Copy of applicant Qatar ID card.
Copy of Commercial License.
Copy of commercial registration.
Copy of establishment ID card.
Fill out the form to be submitted at MoPH.
Attach all the required documents PMS not required
Pay appropriate fees.

Additional Comments

Medical devices must be authorized by one of the founding members of the Global Harmonization Task Force (GHTF) to obtain market access. A local authorized representative is required to obtain an import permit.