UDI device identifier
Omron Focus TENS Knee, Replacement Pad PMKNPAD
UDI device identifier 00073796631468 · Omron Healthcare, Inc.
Key facts
| Primary DI | 00073796631468 |
|---|---|
| Brand name | Omron Focus TENS Knee, Replacement Pad |
| Version or model | PMKNPAD |
| Catalog number | PMKNPAD |
| Company | Omron Healthcare, Inc. |
| DUNS number | 054318779 |
| Product code | NUH |
| GMDN term | Transcutaneous electrical stimulation electrode, single-use |
| Premarket submission | K183215 |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Jan 15, 2020 |
| Version date | Aug 2, 2023 |
| Description | Replacement Pad for Focus Knee TENS . The pad is a disposable, conductive adhesive interface and should only be used with the Focus Knee TENS devices. |
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: