← Back to the brief
Original PDF ↗
Saudi Food and Drug Authority (SFDA) · Technical Regulation
Requirements for Unique Device Identification (UDI) for Medical Devices (MDS – REQ 7)
اشتراطات التعريف الفريد للأجهزة (UDI) للأجهزة الطبية (MDS – REQ 7)
Action requiredReference
PublishedJune 16, 2022
Effective—
GazetteNot gazetted
Saudi regulatory updates, in one morning brief
Bawadir tracks what Saudi regulators issue and delivers what needs your attention each working morning. Your email is all we ask for.
Free. One click to unsubscribe, any time.