Spex 1266-3046-800
by Spex Limited
Ref 1266-3046-800
Spex 1266-3046-800 is a wheelchair head/trunk support (EU MDR Class I; FDA Class I; FDA product code IMS, Support, Head And Trunk, Wheelchair) made by Spex Limited, registered in EUDAMED on 3 May 2026 (Basic UDI-DI 94200517LATERALTRUNKRU) and listed in FDA GUDID since 12 Dec 2022 (UDI-DI 09420051706866), active as of 23 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 | Number94200517LATERALTRUNKRU 09420051706866 | Date3 May 2026 | StatusActive |
| United States | GUDID listing GUDID | Number09420051706866 | Date12 Dec 2022 | StatusListed |
Official records
- EUDAMED public site 94200517LATERALTRUNKRU
- AccessGUDID record 09420051706866
Across registries
- EUDAMED Basic UDI-DI 94200517LATERALTRUNKRU registered 3 May 2026 Active
- FDA GUDID UDI-DI 09420051706866 listed 12 Dec 2022 Listed
Timeline
- Listed FDA GUDID 09420051706866
- Registered EUDAMED 94200517LATERALTRUNKRU
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Spex
- Generic name
- Wheelchair head/trunk support, prefabricated
- Device name
- Lateral Trunk support
- Model / Ref / Catalog
- 1266-3046-800
- Primary DI / UDI-DI
- 09420051706866
- Basic UDI-DI
- 94200517LATERALTRUNKRU
- Direct marketing DI
- 09420051706866
- FDA product code
- IMS
- EMDN code
- Y122499 Wheelchairs accessories - other
- GMDN term
- Wheelchair head/trunk support, prefabricated
- Device class
- Class I
- Regulation number
- 890.3910
- EU registration type
- Standard device
- EU market of registration
- Germany
- GUDID distribution status
- In Commercial Distribution
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