UDI device identifier
BF 64059
UDI device identifier 00026072023051 · Allied Medical, LLC
Key facts
| Primary DI | 00026072023051 |
|---|---|
| Brand name | BF |
| Version or model | 64059 |
| Company | Allied Medical, LLC |
| DUNS number | 119066872 |
| Product code | BYG |
| GMDN term | Aerosol face mask, non-rebreathing |
| Device class | Class I |
| Single use | Yes |
| Packaged sterile | No |
| Implantable | No |
| Publish date | May 28, 2024 |
| Version date | Oct 13, 2025 |
| Description | MASK,ADULT, NON-REB,W/O SAFETY |
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: