UDI device identifier
BROSELOW™ 7730ALS
UDI device identifier 10889483589151 · AIRLIFE
Key facts
| Primary DI | 10889483589151 |
|---|---|
| Brand name | BROSELOW™ |
| Version or model | 7730ALS |
| Catalog number | 7730ALS |
| Company | AIRLIFE |
| DUNS number | 119058668 |
| Product code | OKI |
| GMDN term | Cardiopulmonary resuscitation kit, single-use |
| Device class | Class II |
| Single use | No |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Feb 14, 2025 |
| Version date | Apr 17, 2025 |
| Description | Broselow Domestic Complete ALS Organizer |
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: