UDI device identifier
DLP® 12110
UDI device identifier 20643169880676 · MEDTRONIC, INC.
Key facts
| Primary DI | 20643169880676 |
|---|---|
| Brand name | DLP® |
| Version or model | 12110 |
| Company | MEDTRONIC, INC. |
| DUNS number | 006261481 |
| Product code | DWF |
| GMDN term | Cardiopulmonary bypass/extracorporeal membrane oxygenation cannula, return |
| Premarket submission | K834039 |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | Yes |
| Implantable | No |
| Publish date | Feb 12, 2018 |
| Version date | Jun 19, 2024 |
| Description | SUCTION 12110 LV VENT 10FR PVC 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: