UDI device identifier
Ivenix, Inc. 2.0
UDI device identifier 00811505030122 · Fresenius Kabi AG
Key facts
| Primary DI | 00811505030122 |
|---|---|
| Brand name | Ivenix, Inc. |
| Version or model | 2.0 |
| Catalog number | LVP-SW-0001 |
| Company | Fresenius Kabi AG |
| DUNS number | 315654579 |
| Product code | FRN |
| GMDN term | Bedside infusion pump, single-channel |
| Device class | Class II |
| Single use | No |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Aug 6, 2020 |
| Version date | Aug 21, 2023 |
| Description | Large Volume Pump (LVP) Software (order 1 per pump), version 2.0 |
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: