Motion composites Helio A6
Part of a family of 8 devices: see the family page
Ref Helio A6
Motion composites Helio A6 is a wheelchair (EU MDR Class I; FDA Class I; FDA product code IOR, Wheelchair, Mechanical) made by Motion Composites, registered in EUDAMED on 13 May 2026 (Basic UDI-DI 81177400MCMANUALWC2020FH) and listed in FDA GUDID since 24 Sep 2022 (UDI-DI 00811774000062), active as of 25 Oct 2026.
Active
CE MDR
Valid until
No date given
FDA recalls
Not checked
Documents
None linked in EUDAMED
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR EUDAMED | Number81177400MCMANUALWC2020FH 00811774000062 | Date13 May 2026 | StatusActive |
| United States | GUDID listing GUDID | Number00811774000062 | Date24 Sep 2022 | StatusListed |
Official records
- EUDAMED public site 81177400MCMANUALWC2020FH
- AccessGUDID record 00811774000062
Across registries
- EUDAMED Basic UDI-DI 81177400MCMANUALWC2020FH registered 13 May 2026 Active
- FDA GUDID UDI-DI 00811774000062 listed 24 Sep 2022 Listed
Timeline
- Listed FDA GUDID 00811774000062
- Registered EUDAMED 81177400MCMANUALWC2020FH
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Motion composites
- Generic name
- Wheelchair, attendant/occupant-driven, rear-wheels-operated, collapsible
- Device name
- Manual Wheelchairs
- Model / reference
- Helio A6
- Primary DI / UDI-DI
- 00811774000062
- Basic UDI-DI
- 81177400MCMANUALWC2020FH
- Direct marketing DI
- 00811774000062
- FDA product code
- IOR
- EMDN code
- Y122103 Push wheelchairs
- GMDN term
- Wheelchair, attendant/occupant-driven, rear-wheels-operated, collapsible
- Device class
- Class I
- Regulation number
- 890.3850
- EU registration type
- Standard device
- EU market of registration
- Austria
- GUDID distribution status
- In Commercial Distribution
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