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Lifteo MLA

by Meden-Inmed Sp. Z O.O. EUDAMED

Active European Union

Model Leno, Vista ,Patihoist, Lifteo, Tonya, Levitop, Diana II

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number590368480M005BH Basic UDI-DIDate3 Mar 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

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

Specification

EUDAMED

Device Name
Podnośnik pacjenta, Podnośnik mobilny
Model / Reference
Leno, Vista, Patihoist, Lifteo, Tonya, Levitop, Diana II
Primary DI / UDI-DI
05903684800360
Basic UDI-DI
590368480M005BH
EMDN Code
V0805030102 Electric mobile lifts
Device Class
Class I
Market of Registration
Poland

Manufacturer details

EUDAMED SRN
PL-MF-000001670

Other devices from Meden Inmed Sp Z O O

See all devices from Meden Inmed Sp Z O O →

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