UDI device identifier
Omron Max Power Relief TENS Therapy Pain Relief PM500
UDI device identifier 00073796635008 · Omron Healthcare, Inc.
Key facts
| Primary DI | 00073796635008 |
|---|---|
| Brand name | Omron Max Power Relief TENS Therapy Pain Relief |
| Version or model | PM500 |
| Catalog number | PM500 |
| Company | Omron Healthcare, Inc. |
| DUNS number | 054318779 |
| Product code | NYN |
| GMDN term | Analgesic transcutaneous electrical nerve stimulation system |
| Premarket submission | K182120 |
| Device class | Class II |
| Single use | No |
| Packaged sterile | No |
| Implantable | No |
| Publish date | May 6, 2019 |
| Version date | May 16, 2025 |
| Description | Omron TENS Unit with 9 preset modes and 15 intensity levels. |
At a glance
- 1–9 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: