UDI device identifier
MiAR™ Aortic Root Cannula with Flow-Guard™ 11012L
UDI device identifier 20613994495468 · MEDTRONIC, INC.
Key facts
| Primary DI | 20613994495468 |
|---|---|
| Brand name | MiAR™ Aortic Root Cannula with Flow-Guard™ |
| Version or model | 11012L |
| Company | MEDTRONIC, INC. |
| DUNS number | 006261481 |
| Product code | DWF |
| GMDN term | Cardioplegia cannula |
| Premarket submission | K100274 |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | Yes |
| Implantable | No |
| Publish date | May 21, 2016 |
| Version date | Nov 6, 2023 |
| Description | CANNULA 11012L AR FLOWGUARD LNG 12GA 10P |
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: