UDI device identifier
Switch-It Dual Pro Dual Pro
UDI device identifier 00016958060812 · SUNRISE MEDICAL (US) LLC
Key facts
| Primary DI | 00016958060812 |
|---|---|
| Brand name | Switch-It Dual Pro |
| Version or model | Dual Pro |
| Catalog number | SWI |
| Company | SUNRISE MEDICAL (US) LLC |
| DUNS number | 962525056 |
| Product code | KNO |
| GMDN term | Wheelchair steering/control unit |
| Device class | Class I |
| Single use | No |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Sep 14, 2023 |
| Version date | May 20, 2025 |
| Description | The Dual Pro is a truly proportional head array with fine-tuned adjustments and configurability to provide the user an easy-to-learn, precise, and intuitive driving experience. |
At a glance
- None MAUDE reports citing this UDI
- No Linked premarket submission
- Yes 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: