UDI device identifier
DUO-VENT ACT5439
UDI device identifier 00085412079691 · BAXTER HEALTHCARE CORPORATION
Key facts
| Primary DI | 00085412079691 |
|---|---|
| Brand name | DUO-VENT |
| Version or model | ACT5439 |
| Catalog number | ACT5439 |
| Company | BAXTER HEALTHCARE CORPORATION |
| DUNS number | 005083209 |
| Product code | FPA |
| GMDN term | Basic intravenous administration set, noninvasive |
| Premarket submission | K142011 |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | Yes |
| Implantable | No |
| Publish date | Sep 24, 2016 |
| Version date | Mar 4, 2026 |
| Description | Solution Set with DUO-VENT Spike, 2 Injection Sites, Male Luer Lock Adapter with Retractable Collar |
At a glance
- 1–9 MAUDE reports citing this UDI
- Yes 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: