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Foot Control LiNX

by mo-vis bv

Ref P021-53Model P021

Foot Control LiNX (P021-53) is an assistive rotating/sliding positioning system (EU MDR Class I; FDA Class I; FDA product code KNN, Components, Wheelchair) made by mo-vis bv, registered in EUDAMED on 5 Jun 2023 (Basic UDI-DI 540700832FOOTCONTROL35) and listed in FDA GUDID since 3 Apr 2023 (UDI-DI 05407008321048), active as of 22 Oct 2026.

Active European Union. Also listed in GUDID (US).

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Source EUDAMED, GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number540700832FOOTCONTROL35 Basic UDI-DI 05407008321048UDI-DIDate5 Jun 2023RegisteredStatusActive
United StatesGUDID listing GUDID Number05407008321048 UDI-DI Date3 Apr 2023ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 540700832FOOTCONTROL35 registered 5 Jun 2023 Active
  • FDA GUDID UDI-DI 05407008321048 listed 3 Apr 2023 Listed

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Timeline

2 dated events

  1. Listed FDA GUDID 05407008321048
  2. Registered EUDAMED 540700832FOOTCONTROL35

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade name
Foot Control LiNX EUDAMED
mo-Vis GUDID
Generic name
Assistive rotating/sliding positioning system
Device name
Foot Control
Model / reference
P021, P021-53
Primary DI / UDI-DI
05407008321048
Basic UDI-DI
540700832FOOTCONTROL35
FDA product code
KNN
EMDN code
Y122403 Wheelchair footrests, supports and controls
GMDN term
Assistive rotating/sliding positioning system
Device class
Class I
Regulation number
890.3920
EU registration type
Standard device
EU market of registration
Belgium
GUDID distribution status
In Commercial Distribution

Manufacturer details

EUDAMED SRN
BE-MF-000000729

Similar devices in this category

Other devices filed under WHEELCHAIR FOOTRESTS, SUPPORTS AND CONTROLS.

Other devices from mo-vis bv

See all devices from mo-vis bv →

Properties

  • Single use
  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (21, all answered No)