UDI device identifier
Omron Pain Relief Pro PM3031CAN
UDI device identifier 00073796633141 · Omron Healthcare, Inc.
Key facts
| Primary DI | 00073796633141 |
|---|---|
| Brand name | Omron Pain Relief Pro |
| Version or model | PM3031CAN |
| Catalog number | PM3031CAN |
| Company | Omron Healthcare, Inc. |
| DUNS number | 054318779 |
| Product code | NUH |
| GMDN term | Analgesic transcutaneous electrical nerve stimulation system |
| Premarket submission | K110068 |
| Device class | Class II |
| Single use | No |
| Packaged sterile | No |
| Implantable | No |
| Publish date | May 17, 2017 |
| Version date | Jun 4, 2025 |
| Description | Electrotherapy Pain Relief TENS Unit |
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: