UDI device identifier
Fem-Flex II Femoral Arterial Cannula FEMII016AS
UDI device identifier 00690103168341 · Edwards Lifesciences LLC
Key facts
| Primary DI | 00690103168341 |
|---|---|
| Brand name | Fem-Flex II Femoral Arterial Cannula |
| Version or model | FEMII016AS |
| Catalog number | FEMII016AS |
| Company | Edwards Lifesciences LLC |
| DUNS number | 134139174 |
| Product code | DWF |
| GMDN term | Cardiopulmonary bypass/extracorporeal membrane oxygenation cannula, drainage |
| Premarket submission | K140208 |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | Yes |
| Implantable | No |
| Publish date | Aug 31, 2016 |
| Version date | Jun 19, 2024 |
| Description | FEM-FLEX II Femoral Arterial Cannula |
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: