UDI device identifier
Quickie P-222 P222
UDI device identifier 00016958043419 · SUNRISE MEDICAL (US) LLC
Key facts
| Primary DI | 00016958043419 |
|---|---|
| Brand name | Quickie P-222 |
| Version or model | P222 |
| Catalog number | EIPW2 |
| Company | SUNRISE MEDICAL (US) LLC |
| DUNS number | 962525056 |
| Product code | ITI |
| GMDN term | Electric-motor-driven wheelchair, occupant-controlled |
| Premarket submission | K981462 |
| Device class | Class II |
| Single use | No |
| Packaged sterile | No |
| Implantable | No |
| Publish date | May 3, 2021 |
| Version date | May 20, 2025 |
| Description | The powerful and sleek Quickie® P-222 SE power wheelchair offers you the ultimate in indoor and outdoor maneuverability and performance. Its rear-wheel drive base, sporty frame, and manual conversion kit ensure you arrive confidently and in style. |
At a glance
- None MAUDE reports citing this UDI
- Yes 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: