Jenx JL15
by Jenx Limited
Ref JL15
Jenx JL15 is a Class I device made by Jenx Limited, registered in EUDAMED on 3 Jun 2026 (Basic UDI-DI 50562352POSTURESYSACC4F) and listed in FDA GUDID since 29 Sep 2023 (UDI-DI 05056235205531), active as of 22 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 | Number50562352POSTURESYSACC4F 05056235205531 | Date3 Jun 2026 | StatusActive |
| United States | GUDID listing GUDID | Number05056235205531 | Date29 Sep 2023 | StatusListed |
Official records
- EUDAMED public site 50562352POSTURESYSACC4F
- AccessGUDID record 05056235205531
Across registries
- EUDAMED Basic UDI-DI 50562352POSTURESYSACC4F registered 3 Jun 2026 Active
- FDA GUDID UDI-DI 05056235205531 listed 29 Sep 2023 Listed
Timeline
- Listed FDA GUDID 05056235205531
- Registered EUDAMED 50562352POSTURESYSACC4F
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- LEGACY SPARE Junior Footplate With Medium Bracket EUDAMEDJenx GUDID
- Generic name
- Footrest
- Device name
- Accessories
- Model / reference
- JL15
- Primary DI / UDI-DI
- 05056235205531
- Basic UDI-DI
- 50562352POSTURESYSACC4F
- FDA product code
- INN
- EMDN code
- Y180980 Seating systems / posture systems / seating aids - accessories
- GMDN term
- Footrest
- Device class
- Class I
- Regulation number
- 890.3100
- EU registration type
- Standard device
- EU market of registration
- Norway
- GUDID distribution status
- In Commercial Distribution
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