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artosy

by METEK Köber & Michalski OHG EUDAMED

Active European Union

Ref ergo, buggy

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number426248098artosyMP Basic UDI-DIDate22 May 2024RegisteredStatusActive

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  • Withdrawn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

Device Name
artosy buggy
Model / Reference
ergo, buggy
Primary DI / UDI-DI
04262480980029, 04262480980012
Basic UDI-DI
426248098artosyMP
Direct Marketing DI
04262480980029
04262480980012
EMDN Code
Y122199 Wheelchairs - other
Device Class
Class I
Market of Registration
Austria
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000039613

Other devices from METEK Köber & Michalski OHG

See all devices from METEK Köber & Michalski OHG →

Properties

Show properties
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