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Nemo

by Orthos XXI, Unipessoal Lda 2 variants

Ref 53CD2NE3137ED, 53CD2NE1925ED, 53CD2NE2531ED, 53CDNECONFIGModel Nemo

Nemo (53CD2NE3137ED) is a Class I device made by Orthos XXI, Unipessoal Lda, registered in EUDAMED on 26 Mar 2026 (Basic UDI-DI 56004569NEMONG), active as of 24 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 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number56004569NEMONG Basic UDI-DI Date26 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  • Withdrawn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
Nemo, 53CD2NE3137ED, 53CD2NE1925ED, 53CD2NE2531ED, 53CDNECONFIG
Primary DI / UDI-DI
05600456920409, 05600456920386, 05600456920393, 05600456920416
Basic UDI-DI
56004569NEMONG
Direct marketing DI
05600456920409
05600456920386
05600456920393
05600456920416
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)