Welcome to Medical Regulations Gate
Medical Regulation GateMedical Regulation GateMedical Regulation Gate
(Sat - Thursday)
Kingdom of Saudi Arabia
Medical Regulation GateMedical Regulation GateMedical Regulation Gate

SFDA’s Announcement About Detailed Fees For Updating Medical Device Marketing Authorization (MDMA) Applications.

  • Home
  • Announcements
  • SFDA’s Announcement About Detailed Fees For Updating Medical Device Marketing Authorization (MDMA) Applications.
Medical Regulations Gate - Importation Requirements of Medical Devices - Radioactive Materials - Particle Accelerators - Marketing Authorization Applications - Medical Masks and Particulate Respirators - Quality Management System - Products Classification Guidance - mdma registration - compliance timeframe for medical devices - Guidance on artificial intelligence - Medical ultraviolet radiation
  • January 14, 2021

SFDA has recently announced the detailed fees for updating medical device marketing authorization (MDMA) applications; Click here to read the official document.

Published On: 13 January 2021

 
 
 
 
 
 
 
 

 

Highlights from this Document

This announcement would like to clarify the detailed fees for updating Medical Device Marketing Authorization (MDMA) applications.

This guidance applies to local and overseas medical device manufacturers and Authorized Representatives.

 

 

 
 

For any questions, please drop us a message and we will contact you shortly

 

SFDA’s Draft Guidance of Requirements of Licensing Service Providers for Quality Assurance and Ionizing Radiation Measurements in Healthcare Facilities.
SFDA’s Guidance For Medical Device Maintenance Facilities