At a glance
- Short name
- UDI
- Jurisdiction
- US
- Sectors
- Medical Device, Medtech, Healthcare
- Also known as / related labels
- 21 CFR Part 801 Subpart B · 21 CFR Part 830 · EU MDR Article 27 · IMDRF UDI Guidance
What this entry covers
Evaluate Unique Device Identification compliance for FDA (21 CFR Part 801/830) and EU MDR (Article 27), covering UDI assignment, labeling, GUDID/EUDAMED registration
MyRHC indexes this framework so practitioners, auditors, and automated agents can find the authoritative primary sources in one place. This page is a navigation aid — it is not legal advice and is not a substitute for the official text.
Official documentation
- Primary official source: https://www.fda.gov/medical-devices/device-labeling/unique-device-identification-system-udi-system
How to use this index entry
- Open the official link above (or the agency home if the deep link drifts).
- Confirm edition / revision date against your program scope.
- Map applicability by sector and jurisdiction listed in the metadata.
- Follow related frameworks only after checking their own official sources.
Disclaimers
- MyRHC does not host proprietary standards text (ISO, some industry bodies).
- Where standards are paywalled, we link to the publisher’s catalog page.
- Always verify current requirements with counsel and the issuing authority.
Index only — not legal advice.
MyRHC does not certify compliance. Confirm current requirements with the issuing authority and qualified counsel. Proprietary standards text remains with its publisher.