Skip to content

MindMotion™ PRO

by Mindmaze SA

Ref MMP-01

MindMotion™ PRO (MMP-01) is a Class I device made by MindMaze SA, registered in EUDAMED on 1 Apr 2022 (Basic UDI-DI B-03760272650125), withdrawn as of 24 Oct 2026.

Withdrawn Withdrawn in European Union. No longer placed on the EU market.

Was authorized under CE MDD, withdrawn

Ended

Withdrawn

Date not published (CE MDD)

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Source EUDAMED, synced 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-03760272650125 Basic UDI-DI 03760272650125UDI-DIDate1 Apr 2022RegisteredStatusWithdrawn No longer placed on the EU market

Official records

Certificates

0 certificates · EUDAMED

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

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDD Withdrawn

Specification

EUDAMED

Model / reference
MMP-01
Primary DI / UDI-DI
03760272650125
Basic UDI-DI
B-03760272650125
EMDN code
Z12069099 Various physiotherapy and rehabilitation instruments - other
Device class
Class I
System or procedure pack
System which is a device in itself
EU registration type
Legacy device (under a directive)
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
CH-MF-000022225
Authorised representative
Genious Healthcare SAS FR-AR-000020824

Similar devices in this category

Other devices filed under VARIOUS PHYSIOTHERAPY AND REHABILITATION INSTRUMENTS - OTHER.

Other devices from MindMaze SA

  • MindMotionPRO

    Class II

  • MindMotion GO

    Class II

Properties

Other properties (12, all answered No)