UDI device identifier
AirLife™ AH265
UDI device identifier 10190752145160 · AIRLIFE
Key facts
| Primary DI | 10190752145160 |
|---|---|
| Brand name | AirLife™ |
| Version or model | AH265 |
| Catalog number | AH265 |
| Company | AIRLIFE |
| DUNS number | 119058668 |
| Product code | OFP |
| GMDN term | Inspiratory line humidification chamber, single-use |
| Device class | Class I |
| Single use | Yes |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Jan 15, 2020 |
| Version date | Apr 17, 2025 |
| Description | AirLife™ Infant Heated Wire Circuit Kit Dual-limb, Dual-heat, high-flow circuit (>4 L/min) Contains AH165 Circuit, AH290 Chamber |
At a glance
- None MAUDE reports citing this UDI
- No Linked premarket submission
- No EUDAMED counterpart found
- 100–999 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: