SFDA MDS-REQ-007-V4MDS-REQ-007-V4/220524
Currentness under review. Whether this instrument remains applicable is under review. Consult the later instruments and source context below before relying on it.
MDS-REQ-007-V4/220524 is the official SFDA identifier for “Unique Device Identification requirements — Version 4.0, 24 May 2022”. MDS-REQ-007-V4/220524 is the official identifier SFDA uses for this instrument.
- Instrument
- MDS-REQ-007-V4
- Full name
- MDS-REQ-007-V4/220524
- Category
- Registration
- Source publication
- English
- Readable HTML
- 1 language version
- Published
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- Effective
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Each version has stable passage anchors for direct citations and highlighting. The readable text is generated from an authority source and does not replace the legally controlling publication.
Unique Device Identification requirements — Version 4.0, 24 May 2022
All 20 physical pages of the exact official English MDS-REQ7 Version4.0 expression, including general/direct-marking requirements, UDI-DI lifecycle, Saudi-DI data fields, additional device requirements, implementation provisions and both annexes. Printed 24 May 2022 is the document version date, not an inferred legal commencement date. Scope covers marketed devices/supplies/accessories not exempted from marketing authorization, plus manufacturers and authorized representatives. Source preservation does not by itself newly verify an existing question answer, present-day consolidated legal currentness, or universal REF/SMN-to-UDI equivalence. The exact registry URL ending RequirementsUDI_0.pdf was directly captured 26 October 2026 with target200; older identical bytes at RequirementsUDI.pdf are separate provenance, not an inferred redirect. Source images govern; the embedded text is a qualified search layer. No whole-country completeness claim.
MDS-REQ-007-V4/220524 is the official identifier SFDA uses for this instrument. Always confirm the current consolidated text and transition provisions with the official source before filing.