UDI device identifier
Carex FGR10300 0000
UDI device identifier 00023601061034 · Drive Devilbiss Healthcare
Key facts
| Primary DI | 00023601061034 |
|---|---|
| Brand name | Carex |
| Version or model | FGR10300 0000 |
| Company | Drive Devilbiss Healthcare |
| DUNS number | 867673159 |
| Product code | BYX |
| GMDN term | Oxygen administration tubing |
| Device class | Class I |
| Single use | No |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Jun 7, 2023 |
| Version date | May 27, 2026 |
| Description | Ped.Cannula w/ 7' tubing |
At a glance
- None MAUDE reports citing this UDI
- No Linked premarket submission
- No EUDAMED counterpart found
- 1,000+ GUDID devices with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About UDI device identifiers (GUDID)
The Global Unique Device Identification Database (GUDID) holds the device identifiers (UDI-DIs) and key attributes that labelers submit to the FDA for devices that carry a unique device identifier.
Source: U.S. FDA Global Unique Device Identification Database (GUDID), via NLM AccessGUDID · Source date: