$16
FDA 21 CFR PART 830
2018
UNIQUE DEVICE IDENTIFICATION
- Format:
- Language(s) :
- Published :
- English
- 04/01/2018
Definitions.
As used in this part:
Automatic identification and data capture (AIDC) means any technology that conveys the unique device identifier or the device identifier of a device in a form that can be entered into an electronic patient record or other computer system via an automated process.
| FDA 21 CFR PART 830 | |
|---|---|
| STANDARD INFO: | |
| Standard Name | FDA 21 CFR PART 830 |
| Scope | UNIQUE DEVICE IDENTIFICATION |
| Publisher | FDA - Food and Drug Administration |
| Languages | English |
| State | [ Revised ] |
| Publication Year | 2018 |
| Most recent Version | FDA 21 CFR PART 830 |
| Whether to be replaced | View the most recent version. |
| Addendum | |
| FILE INFO: | |
| Edition | 18 |
| File Size | 1 file , 210 KB |
| Number of Pages | 9 |
| Published | 04/01/2018 |
| FDA 21 CFR PART 830 | ||
|---|---|---|
| History | Publisher Year | |
| FDA 21 CFR PART 830 | 2019 | |
| FDA 21 CFR PART 830 | 2018 | Current |
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