UDI device identifier
DUPLOCATH 1506166
UDI device identifier 00085412600031 · BAXTER INTERNATIONAL INC.
Key facts
| Primary DI | 00085412600031 |
|---|---|
| Brand name | DUPLOCATH |
| Version or model | 1506166 |
| Catalog number | 1506166 |
| Company | BAXTER INTERNATIONAL INC. |
| DUNS number | 005146311 |
| Product code | FMF |
| GMDN term | Open-surgery adhesive/sealant applicator, dual-channel |
| Premarket submission | BK170033 |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | Yes |
| Implantable | No |
| Publish date | Sep 28, 2018 |
| Version date | Jul 10, 2023 |
| Description | Catheter for the simultaneous application of Baxter two-component fibrin sealant in minimally invasive surgery. The application of Baxter's two-component fibrin sealant can be carried out via a double syringe system and the two-lumen Duplocath application catheter. |
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: