Quickie Xenon
Quickie Xenon (EIX2) is a push-rim manual wheelchair (FDA Class I; FDA product code IOR, Wheelchair, Mechanical) made by Sunrise Medical (US) LLC, listed in FDA GUDID since 2 Sep 2023 (UDI-DI 00016958056198), registry data as of 15 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00016958056198 | Date2 Sep 2023 | StatusListed |
Official records
- AccessGUDID record 00016958056198
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Generic name
- Push-rim manual wheelchair, non-bariatric
- Model / Ref / Catalog
- Xenon2, Xenon2 FF, Xenon2 Hybrid, Xenon2 SA, EIX2
- Primary DI / UDI-DI
- 00016958056198
- FDA product code
- IOR
- GMDN term
- Push-rim manual wheelchair, non-bariatric
- Device class
- Class I
- Regulation number
- 890.3850
- GUDID distribution status
- In Commercial Distribution
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Other devices filed under FDA product code IOR (Wheelchair, Mechanical).
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- SPECTRUM SPIRIT by FREEDOM DESIGNS, INC.