UDI device identifier
CLEARLINK/DUO-VENT 2R8480
UDI device identifier 00085412565750 · BAXTER INTERNATIONAL INC.
Key facts
| Primary DI | 00085412565750 |
|---|---|
| Brand name | CLEARLINK/DUO-VENT |
| Version or model | 2R8480 |
| Catalog number | 2R8480 |
| Company | BAXTER INTERNATIONAL INC. |
| DUNS number | 005146311 |
| Product code | FPA |
| GMDN term | Intravenous line filter |
| Premarket submission | K153158 |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | Yes |
| Implantable | No |
| Publish date | Jul 11, 2017 |
| Version date | Jul 6, 2018 |
| Description | Non-DEHP Solution Set with DUO-VENT Spike, 0.2 Micron Downstream Filter, Luer Activated Valve Male Luer Lock Adapter with Retractable Collar, 103" 2.6m approx., 10 drops/mL approx. |
At a glance
- 10–99 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: