UDI device identifier
TFX-LT2000 Therapy Light TFX-LT2000
UDI device identifier 00086001245602 · ToeFX Inc
Key facts
| Primary DI | 00086001245602 |
|---|---|
| Brand name | TFX-LT2000 Therapy Light |
| Version or model | TFX-LT2000 |
| Company | ToeFX Inc |
| DUNS number | 202099070 |
| Product code | PDZ |
| GMDN term | Nail laser phototherapy unit |
| Device class | Class II |
| Single use | No |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Nov 15, 2024 |
| Version date | Nov 25, 2024 |
| Description | Light therapy device for onychomycosis |
At a glance
- None MAUDE reports citing this UDI
- No Linked premarket submission
- No EUDAMED counterpart found
- 1–9 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: