UDI device identifier
FUTURO™ 71059EN
UDI device identifier 00051131201644 · 3M COMPANY
Key facts
| Primary DI | 00051131201644 |
|---|---|
| Brand name | FUTURO™ |
| Version or model | 71059EN |
| Catalog number | 71059EN |
| Company | 3M COMPANY |
| DUNS number | 830016148 |
| Product code | DWL |
| GMDN term | Compression/pressure sock/stocking, single-use |
| Device class | Class II |
| Single use | No |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Jul 21, 2016 |
| Version date | Jul 7, 2020 |
| Description | 71059EN FUTURO(TM) ANTI-EMBOLISM STOCKINGS, KNEE, LENGTH, CLOSED TOE, EXTRA LARGE REGULAR, WHITE |
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: