UDI device identifier
RGK Octane FX FX
UDI device identifier 00016958060249 · SUNRISE MEDICAL (US) LLC
Key facts
| Primary DI | 00016958060249 |
|---|---|
| Brand name | RGK Octane FX |
| Version or model | FX |
| Company | SUNRISE MEDICAL (US) LLC |
| DUNS number | 962525056 |
| Product code | IOR |
| GMDN term | Push-rim manual wheelchair, non-bariatric |
| Device class | Class I |
| Single use | No |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Sep 5, 2023 |
| Version date | Nov 24, 2025 |
| Description | The RGK Octane FX is a made-to-measure chair unlike any other. Imagine a wheelchair that folds down so small you can store it in most airplane overhead luggage compartments. Imagine a wheelchair that is as lightweight and performance-oriented as a rigid sports chair. |
At a glance
- None MAUDE reports citing this UDI
- No Linked premarket submission
- No EUDAMED counterpart found
- 1,000+ 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: