UDI device identifier
Foredom K.500
UDI device identifier 00098666032305 · Foredom Electric Co
Key facts
| Primary DI | 00098666032305 |
|---|---|
| Brand name | Foredom |
| Version or model | K.500 |
| Company | Foredom Electric Co |
| DUNS number | 048343438 |
| Product code | ISA |
| GMDN term | Hand-held electric massager |
| Device class | Class I |
| Single use | No |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Aug 30, 2023 |
| Version date | Sep 7, 2023 |
| Description | Foredom powered 39" flexible shaft machine, includes Hand-held Massager Handpiece. |
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: