FDA 2121 CFR Part 830
Unique Device Identification
United StatesFDAUDIEffective September 24, 2013
What this code is
21 CFR Part 830 is the official FDA identifier for “Unique Device Identification”. 21 CFR Part 830 is the official identifier FDA uses for this instrument.
- Instrument
- 21
- Full name
- 21 CFR Part 830
- Category
- UDI
Source links
- Authority source
- English
- Readable HTML
- 20 articles · 1 language version
Issuing-authority publication; confirm whether a later amendment or consolidated version applies.
Direct citations can link to a specific article or section by appending its fragment identifier.
Dates
- Published
- September 24, 2013
- Effective
- September 24, 2013
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About this regulation
Unique Device Identification
Current eCFR Part 830 unique device identification requirements.
21 CFR Part 830 is the official identifier FDA uses for this instrument. Always confirm the current consolidated text and transition provisions with the official source before filing.