UDI device identifier
HOMEDICS TIE-240-BABY
UDI device identifier 00031262101235 · FKA DISTRIBUTING CO., LLC
Key facts
| Primary DI | 00031262101235 |
|---|---|
| Brand name | HOMEDICS |
| Version or model | TIE-240-BABY |
| Company | FKA DISTRIBUTING CO., LLC |
| DUNS number | 183280973 |
| Product code | FLL |
| GMDN term | Infrared patient thermometer, skin |
| Device class | Class II |
| Single use | No |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Jan 11, 2021 |
| Version date | Jan 19, 2021 |
| Description | Non-contact Infrared Body Thermometer |
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: