UDI device identifier
Footsure 60250
UDI device identifier 00084025290158 · Therafin Corporation
Key facts
| Primary DI | 00084025290158 |
|---|---|
| Brand name | Footsure |
| Version or model | 60250 |
| Catalog number | 60250 |
| Company | Therafin Corporation |
| DUNS number | 056630924 |
| Product code | KNO |
| GMDN term | Wheelchair footrest/legrest |
| Device class | Class I |
| Single use | No |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Jul 6, 2023 |
| Version date | Sep 11, 2026 |
| Description | FOOTSURE ANKLE SUPPORT WITH BUCKLE, X-SMALL PAIR 00084025290158 was a typo, it was supposed to be 00840252901584. This incorrect record has been discontinued. A new record created for the corrected Primary DI Number. All product had been labeled correctly with 00840252901584. |
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: