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Liliput

by Orthos XXI, Unipessoal Lda 5 variants

Part of a family of 11 devices: see the family page

Ref 53CDLICONFIGModel Liliput

Liliput (53CDLICONFIG) is a Class I device made by Orthos XXI, Unipessoal Lda, registered in EUDAMED on 26 Mar 2026 (Basic UDI-DI 56004569LILIPUTSC), active as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number56004569LILIPUTSC Basic UDI-DI 05600456920140UDI-DIDate26 Mar 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  • Withdrawn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
Cadeira de Rodas
Model / reference
Liliput, 53CDLICONFIG
Primary DI / UDI-DI
05600456920140
Basic UDI-DI
56004569LILIPUTSC
Direct marketing DI
05600456920140
EMDN code
Y122106 Rear self-propelled wheelchairs
Device class
Class I
EU registration type
Standard device
EU market of registration
Portugal

Manufacturer details

EUDAMED SRN
PT-MF-000002787

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Properties

Other properties (14, all answered No)