UDI device identifier
BD Alaris 8100
UDI device identifier 10885403517723 · CAREFUSION 303, INC.
Key facts
| Primary DI | 10885403517723 |
|---|---|
| Brand name | BD Alaris |
| Version or model | 8100 |
| Company | CAREFUSION 303, INC. |
| DUNS number | 360624720 |
| Product code | FRN |
| GMDN term | Bedside infusion pump, single-channel |
| Device class | Class II |
| Single use | No |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Oct 30, 2023 |
| Version date | Aug 19, 2024 |
| Description | BD Alaris Pump Module (REM V12.1.2+) |
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: