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Twister Basic, (300mm), Green

by mo-vis bv

Part of a family of 50 devices: see the family page

Ref P005-19

Twister Basic, (300mm), Green (P005-19) is an assistive input-control operation training device (EU MDR Class I; FDA Class I; FDA product code KNN, Components, Wheelchair) made by mo-vis bv, registered in EUDAMED on 26 Mar 2025 (Basic UDI-DI 540700832TWISTERSB) and listed in FDA GUDID since 31 Aug 2020 (UDI-DI 05407008320478), 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 linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number540700832TWISTERSB Basic UDI-DI 05407008320478UDI-DIDate26 Mar 2025RegisteredStatusActive
United StatesGUDID listing GUDID Number05407008320478 UDI-DI Date31 Aug 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 540700832TWISTERSB registered 26 Mar 2025 Active
  • FDA GUDID UDI-DI 05407008320478 listed 31 Aug 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 05407008320478
  2. Registered EUDAMED 540700832TWISTERSB

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  • Withdrawn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
Twister Basic, (300mm), Green EUDAMED
mo-Vis GUDID
Generic name
Assistive input-control operation training device, selection techniques
Device name
Twister
Model / reference
P005-19
Primary DI / UDI-DI
05407008320478
Basic UDI-DI
540700832TWISTERSB
FDA product code
KNN
EMDN code
Y122403 Wheelchair footrests, supports and controls
GMDN term
Assistive input-control operation training device, selection techniques
Device class
Class I
Regulation number
890.3920
System or procedure pack
System which is a device in itself
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

  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (22, all answered No)