UDI device identifier
Halyard SELF131-05_0002
UDI device identifier 10809160408650 · AVID MEDICAL, INC.
Key facts
| Primary DI | 10809160408650 |
|---|---|
| Brand name | Halyard |
| Version or model | SELF131-05_0002 |
| Catalog number | SELF131-05 |
| Company | AVID MEDICAL, INC. |
| DUNS number | 015623119 |
| Product code | OEZ |
| GMDN term | Cardiothoracic surgical procedure kit, medicated, single-use |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | Yes |
| Implantable | No |
| Publish date | Sep 11, 2023 |
| Version date | Sep 19, 2023 |
At a glance
- None MAUDE reports citing this UDI
- No 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: