UDI device identifier
CLEARLINK/INTERLINK/DUO-VENT EMS3160
UDI device identifier 00085412082592 · BAXTER HEALTHCARE CORPORATION
Key facts
| Primary DI | 00085412082592 |
|---|---|
| Brand name | CLEARLINK/INTERLINK/DUO-VENT |
| Version or model | EMS3160 |
| Catalog number | EMS3160 |
| Company | BAXTER HEALTHCARE CORPORATION |
| DUNS number | 005083209 |
| Product code | FPA |
| GMDN term | Basic intravenous administration set, noninvasive |
| Premarket submission | K112893 |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | Yes |
| Implantable | No |
| Publish date | Sep 24, 2016 |
| Version date | Sep 25, 2026 |
| Description | Non-DEHP Solution Set with DUO-VENT Spike, Luer Activated Valve, INTERLINK Injection Site, Male Luer Lock Adapter with Retractable Collar |
At a glance
- None 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: