UDI device identifier
Luma Rx SP6800FC
UDI device identifier 00074590543872 · SPECTRUM BRANDS, INC.
Key facts
| Primary DI | 00074590543872 |
|---|---|
| Brand name | Luma Rx |
| Version or model | SP6800FC |
| Company | SPECTRUM BRANDS, INC. |
| DUNS number | 001951946 |
| Product code | ONF |
| GMDN term | Intense pulsed light skin surface treatment system |
| Premarket submission | K140631 |
| Device class | Class II |
| Single use | No |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Sep 30, 2016 |
| Version date | Oct 19, 2021 |
| Description | Consumable compontent for IPL6800 device |
At a glance
- None MAUDE reports citing this UDI
- Yes Linked premarket submission
- No EUDAMED counterpart found
- 100–999 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: