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Wózek specjalny inwalidzki ULISES EVO

by Akces-Med Spółka Z Ograniczoną Odpowiedzialnością 145 variants

Ref ULE

Active European Union

CE MDR

Valid until

Not listed

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

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number59038165ULE3B Basic UDI-DI 05903816529350UDI-DIDate8 Oct 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

NorwayIcelandSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaLiechtensteinAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyTürkiyeCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

EU market availability

Made available in 32 countries, as listed in EUDAMED:

Declared by the manufacturer in EUDAMED for this device version; may not cover every market.

  • Austria since 6 May 2019
  • Belgium since 6 May 2019
  • Bulgaria since 6 May 2019
  • Croatia since 6 May 2019
  • Cyprus since 6 May 2019
  • Czechia since 6 May 2019
  • Denmark since 6 May 2019
  • Estonia since 6 May 2019
  • Finland since 6 May 2019
  • France since 6 May 2019
  • Germany since 6 May 2019
  • Greece since 6 May 2019
  • Hungary since 6 May 2019
  • Iceland since 6 May 2019
  • Ireland since 6 May 2019
  • Italy since 6 May 2019
  • Latvia since 6 May 2019
  • Liechtenstein since 6 May 2019
  • Lithuania since 6 May 2019
  • Luxembourg since 6 May 2019
  • Malta since 6 May 2019
  • Netherlands since 6 May 2019
  • Northern Ireland since 6 May 2019
  • Norway since 6 May 2019
  • Poland since 6 May 2019
  • Portugal since 6 May 2019
  • Romania since 6 May 2019
  • Slovakia since 6 May 2019
  • Slovenia since 6 May 2019
  • Spain since 6 May 2019
  • Sweden since 6 May 2019
  • Türkiye since 6 May 2019

Last checked 27 Oct 2026.

Specification

EUDAMED

Model / Reference
ULE
Primary DI / UDI-DI
05903816529350
Basic UDI-DI
59038165ULE3B
Direct Marketing DI
05903816529350
EMDN Code
Y122703 Pushchairs
Device Class
Class I
EU market of registration
Poland

Manufacturer details

EUDAMED SRN
PL-MF-000003624

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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