UDI device identifier
Ivenix Infusion System SET-0032-1
UDI device identifier 00811505030214 · Fresenius Kabi AG
Key facts
| Primary DI | 00811505030214 |
|---|---|
| Brand name | Ivenix Infusion System |
| Version or model | SET-0032-1 |
| Catalog number | SET-0032-1 |
| Company | Fresenius Kabi AG |
| DUNS number | 315654579 |
| Product code | FPA |
| GMDN term | Electric infusion pump administration set, single-use |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | Yes |
| Implantable | No |
| Publish date | Mar 24, 2022 |
| Version date | Apr 28, 2025 |
| Description | LVP Primary Administration Set, Dual-Inlet, Low-Sorbing, Needle-Free Port, Dual Y-Site (Qty 1) |
At a glance
- None MAUDE reports citing this UDI
- No Linked premarket submission
- No EUDAMED counterpart found
- 1,000+ 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: