UDI device identifier
Lifogen 0022-230P
UDI device identifier 00026072011010 · Allied Medical, LLC
Key facts
| Primary DI | 00026072011010 |
|---|---|
| Brand name | Lifogen |
| Version or model | 0022-230P |
| Catalog number | 31-01-0600 |
| Company | Allied Medical, LLC |
| DUNS number | 119066872 |
| Product code | CAN |
| GMDN term | Fixed-regulator oxygen refillable cylinder |
| Premarket submission | K895956 |
| Device class | Class I |
| Single use | No |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Sep 20, 2016 |
| Version date | Oct 13, 2025 |
| Description | Emergency Oxygen Unit |
At a glance
- None MAUDE reports citing this UDI
- Yes 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: