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Lae

by Levo AG EUDAMED

Active European Union

Ref LAE/S-M/48/57

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number7613045_LAE_2W Basic UDI-DIDate19 Aug 2025RegisteredStatusActive

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  • Withdrawn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
Lae
Model / Reference
LAE/S-M/48/57
Primary DI / UDI-DI
07613045036496
Basic UDI-DI
7613045_LAE_2W
Direct Marketing DI
07613045036496
EMDN Code
Y122199 Wheelchairs - other
Device Class
Class I
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
CH-MF-000008751
Authorised representative
be-on-market GmbH DE-AR-000006148

Other devices from Levo AG

  • C3

    Class I

  • Lcev

    Class I

  • Levo Max

    Class II

  • Levo Comfort Ii

    Class II

  • Levo C3 Standup Wheelchair

    Class II

  • Levo Combi

    Class II

See all devices from Levo AG →

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