UDI device identifier
Alaris 8100
UDI device identifier 10885403810039 · CAREFUSION 303, INC.
Key facts
| Primary DI | 10885403810039 |
|---|---|
| Brand name | Alaris |
| Version or model | 8100 |
| Company | CAREFUSION 303, INC. |
| DUNS number | 360624720 |
| Product code | FRN |
| GMDN term | Bedside infusion pump, single-channel |
| Premarket submission | K072105 |
| Device class | Class II |
| Single use | No |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Nov 6, 2021 |
| Version date | May 6, 2024 |
| Description | Alaris Pump Module |
At a glance
- 1,000+ MAUDE reports citing this UDI
- Yes 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: