Saudi Arabia - MedStandard

Saudi Arabia

Saudi Food and Drug Authority (SFDA)

Interim Order No.1-8-1429 of 2008

English and Arabic

country resident

5–6 months

A brief algorithm for registration of medical devices in Saudi Arabia:

01

Determination of the classification of the device according to the SFDA classification rules

02

Appointment of an Authorized Representative to manage device registration and communicate with SFDA on behalf of the manufacturer

03

Preparation of the technical file and application form for submission to the SFDA

04

State fee payment initiation

05

SFDA reviews the application and may request additional information

06

Upon approval by the SFDA, a certificate of marketing authorization for the medical device will be issued

Final price and terms procedures will be calculated according to your request