UDI device identifier
INTRAVIA 2B8019
UDI device identifier 00085412003504 · BAXTER HEALTHCARE CORPORATION
Key facts
| Primary DI | 00085412003504 |
|---|---|
| Brand name | INTRAVIA |
| Version or model | 2B8019 |
| Catalog number | 2B8019 |
| Company | BAXTER HEALTHCARE CORPORATION |
| DUNS number | 005083209 |
| Product code | KPE |
| GMDN term | Intravenous administration bag/bottle |
| Premarket submission | K964853 |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | Yes |
| Implantable | No |
| Publish date | Sep 24, 2016 |
| Version date | Sep 30, 2026 |
| Description | INTRAVIA Container, 50 mL Capacity |
At a glance
- 10–99 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: