UDI device identifier
Omron Focus TENS Therapy for Knee - Large PM710-L
UDI device identifier 00073796637125 · Omron Healthcare, Inc.
Key facts
| Primary DI | 00073796637125 |
|---|---|
| Brand name | Omron Focus TENS Therapy for Knee - Large |
| Version or model | PM710-L |
| Catalog number | PM710-L |
| Company | Omron Healthcare, Inc. |
| DUNS number | 054318779 |
| Product code | NYN |
| GMDN term | Analgesic transcutaneous electrical nerve stimulation system |
| Premarket submission | K183215 |
| Device class | Class II |
| Single use | No |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Jan 15, 2020 |
| Version date | Jan 23, 2020 |
| Description | Omron TENS unit is wearable and wireless, battery operated and includes the device, case, band and pad. |
At a glance
- None MAUDE reports citing this UDI
- Yes Linked premarket submission
- No EUDAMED counterpart found
- 10–99 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: