UDI device identifier
OptiSite Arterial Perfusion Cannula OPTI16
UDI device identifier 00690103180558 · Edwards Lifesciences LLC
Key facts
| Primary DI | 00690103180558 |
|---|---|
| Brand name | OptiSite Arterial Perfusion Cannula |
| Version or model | OPTI16 |
| Catalog number | OPTI16 |
| Company | Edwards Lifesciences LLC |
| DUNS number | 134139174 |
| Product code | DQR |
| GMDN term | Cardiopulmonary bypass/extracorporeal membrane oxygenation cannula, return |
| Premarket submission | K073559 |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | Yes |
| Implantable | No |
| Publish date | Aug 31, 2016 |
| Version date | Jun 19, 2024 |
| Description | OptiSite Arterial Perfusion Cannula |
At a glance
- None MAUDE reports citing this UDI
- Yes Linked premarket submission
- No EUDAMED counterpart found
- 100–999 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: