If software update for a medical device imported to KSA is released,but this update is only for improvement not due to problem or malfunction in the device,Is it mandatory to inform SFDA about this action and provide all the requirements for its closure?
In case there is a problem or malfunction affects patient or user’s safety, the manufacturer should issue the Field Safety Corrective Action and inform SFDA accordingly.
تصنيف
Comments and Suggestions
For any inquiries or comments about the government services, please fill in the required information.