UDI

Unique Device Identification (UDI) requirements under SFDA MDS-REQ 7 — data submission, labelling, and compliance timelines.

📄️UDI Overview

SFDA Unique Device Identification (UDI) requirements under MDS-REQ 7 — structure, obligations, and differences from US FDA and EU MDR UDI.

How to submit UDI data to the SFDA via GHAD, and the compliance timeline phasing by device class.

UDI placement and format requirements on device labels in Saudi Arabia under MDS-REQ 7.