UDI device identifier
DLP® Aortic Root Cannula with Flow-Guard™ 11012
UDI device identifier 20613994495451 · MEDTRONIC, INC.
Key facts
| Primary DI | 20613994495451 |
|---|---|
| Brand name | DLP® Aortic Root Cannula with Flow-Guard™ |
| Version or model | 11012 |
| Company | MEDTRONIC, INC. |
| DUNS number | 006261481 |
| Product code | DWF |
| GMDN term | Cardioplegia cannula |
| Premarket submission | K790565 |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | Yes |
| Implantable | No |
| Publish date | May 21, 2016 |
| Version date | Jul 6, 2018 |
| Description | CANNULA 11012 AR FLOWGUARD 12GA 20PK 17L |
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: