UDI device identifier
7LS FA7-1400J
UDI device identifier 00031262096531 · FKA DISTRIBUTING CO., LLC
Key facts
| Primary DI | 00031262096531 |
|---|---|
| Brand name | 7LS |
| Version or model | FA7-1400J |
| Catalog number | FA7-1400J |
| Company | FKA DISTRIBUTING CO., LLC |
| DUNS number | 183280973 |
| Product code | NFO |
| GMDN term | Analgesic transcutaneous electrical nerve stimulation system |
| Premarket submission | K162106 |
| Device class | Class II |
| Single use | No |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Feb 29, 2020 |
| Version date | Mar 9, 2020 |
| Description | ReSculpt Micro-Current & Light Therapy |
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: