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Spex

by Spex Ltd New Zealand EUDAMED

Ref 1420-1111-001_054 EMDN Y122406

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number94200517WONDERSEATDT Basic UDI-DIDate7 May 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 25 Oct 2026

Device Name
Spex Wonderseat
Model / Reference
1420-1111-001_054
Primary DI / UDI-DI
09420082911802
Basic UDI-DI
94200517WONDERSEATDT
Direct Marketing DI
09420082911802
EMDN Code
Y122406 Belts, seats and armrests for wheelchairs
Device Class
Class I
Market of Registration
Italy

Manufacturer details

EUDAMED SRN
NZ-MF-000009327
Authorised representative
BEO MedConsulting Berlin GmbH DE-AR-000006764

Other devices from Spex Ltd

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    Class I

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    Class I

  • Spex

    Class I

  • Spex

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  • Spex

    Class I

See all devices from Spex Ltd →

Properties & raw data

Show properties, registry sources and raw records
Other properties (13)
  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No

Sources (1)

  • EUDAMED 09420082911802|94200517WONDERSEATDT 61 fields · synced 25 Oct 2026