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Flipper wheelchair

by Mobilex A/S 4 variants

Ref 271951Model FLIPPER WHEELCHAIR

Flipper wheelchair (271951) is a Class I device made by Mobilex A/S, registered in EUDAMED on 15 Sep 2026 (Basic UDI-DI 57400014FLIPPERER), active as of 25 Oct 2026.

Active European Union

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Source EUDAMED, synced 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number57400014FLIPPERER Basic UDI-DI 05740001403800UDI-DIDate15 Sep 2026RegisteredStatusActive

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  • Withdrawn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/MDR Active

Specification

EUDAMED

Device name
Flipper wheelchair, with options
Model / reference
FLIPPER WHEELCHAIR, 271951
Primary DI / UDI-DI
05740001403800
Basic UDI-DI
57400014FLIPPERER
EMDN code
Y122106 Rear self-propelled wheelchairs
Device class
Class I
EU registration type
Standard device
EU market of registration
Poland

Manufacturer details

EUDAMED SRN
DK-MF-000021885

Similar devices in this category

Other devices filed under REAR SELF-PROPELLED WHEELCHAIRS.

Other devices from Mobilex A/S

See all devices from Mobilex A/S →

Properties

Other properties (14, all answered No)