Skip to content

ProLift A333 CFU

by novacare gmbh Germany EUDAMED

Ref 960506Model Patient Lift

EMDN V0805030102

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number42504796V0805030102EF Basic UDI-DIDate27 Apr 2022RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Not covered

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 22 Oct 2026

Device Name
ProLift Series
Model / Reference
Patient Lift, 960506
Primary DI / UDI-DI
04250479609006
Basic UDI-DI
42504796V0805030102EF
Direct Marketing DI
04250479609006
EMDN Code
V0805030102 Electric mobile lifts
Device Class
Class I
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000007623

Other devices from novacare gmbh

See all devices from novacare gmbh →

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 db390526-c7e6-4579-945c-5f91e0972ced 61 fields · synced 22 Oct 2026