RoughRider Aurora
by Roughrider America LLC 8 variants
RoughRider Aurora is a Class I device made by Roughrider America LLC, listed in FDA GUDID since 1 Mar 2023 (UDI-DI 00860003056660), registry data as of 22 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 | Number00860003056660 | Date1 Mar 2023 | StatusListed |
Official records
- AccessGUDID record 00860003056660
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- RoughRider
- Generic name
- Push-rim manual wheelchair, non-bariatric
- Model / reference
- Aurora
- Primary DI / UDI-DI
- 00860003056660
- 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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