UDI device identifier
Koresway KB05
UDI device identifier 00008600088282 · Diversified Healthcare Development, LLC
Key facts
| Primary DI | 00008600088282 |
|---|---|
| Brand name | Koresway |
| Version or model | KB05 |
| Company | Diversified Healthcare Development, LLC |
| DUNS number | 048174391 |
| Product code | KHX |
| GMDN term | Balance/cognitive function analysis system |
| Device class | Class I |
| Single use | No |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Aug 22, 2023 |
| Version date | Aug 30, 2023 |
| Description | The FDA-listed KoreSway™ Kompact incorporates the patented Korebalance™ software suites into a compact and affordable package. Utilizing proven force transducers and rapid sampling rates, the KoreSway™ captures the minute patient center of gravity movements. Includes a portable safety rail system… |
At a glance
- None MAUDE reports citing this UDI
- No 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: