Surelock 50218
Ref 50218
Surelock 50218 is a Class I device made by Therafin Corporation, registered in EUDAMED on 4 Nov 2026 (Basic UDI-DI 0840252950218TV) and listed in FDA GUDID since 6 Jul 2023 (UDI-DI 00840252901096), active as of 7 Nov 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 | Number0840252950218TV 00840252901096 | Date4 Nov 2026 | StatusActive |
| United States | GUDID listing GUDID | Number00840252901096 | Date6 Jul 2023 | StatusListed |
Official records
- EUDAMED public site 0840252950218TV
- AccessGUDID record 00840252901096
Across registries
- EUDAMED Basic UDI-DI 0840252950218TV registered 4 Nov 2026 Active
- FDA GUDID UDI-DI 00840252901096 listed 6 Jul 2023 Listed
Timeline
- Listed FDA GUDID 00840252901096
- Registered EUDAMED 0840252950218TV
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Headrest Hardware, Surelock Multi-Axis. EUDAMEDSurelock GUDID
- Generic name
- Wheelchair/chair/stander headrest
- Model / Ref / Catalog
- 50218
- Primary DI / UDI-DI
- 00840252901096
- Basic UDI-DI
- 0840252950218TV
- FDA product code
- IMS
- EMDN code
- Y122499 Wheelchairs accessories - other
- GMDN term
- Wheelchair/chair/stander headrest
- Device class
- Class I
- Regulation number
- 890.3910
- EU registration type
- Standard device
- EU market of registration
- France
- GUDID distribution status
- In Commercial Distribution
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