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Enterprise 5000X

by ArjoHuntleigh AB Sweden EUDAMED

Ref E5X3QG113DEABAModel 8X13GY113DCABA

EMDN V08060103

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number5060693520143VW Basic UDI-DIDate3 Jun 2024RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Not covered

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 24 Oct 2026

Device Name
Enterprise 8000X
Model / Reference
8X13GY113DCABA, E5X3QG113DEABA
Primary DI / UDI-DI
05059441379140
Basic UDI-DI
5060693520143VW
EMDN Code
V08060103 Semi-intensive therapy or cardiac intensive care units (cicu) electric medical beds
Device Class
Class I
Market of Registration
France

Manufacturer details

EUDAMED SRN
SE-MF-000000696

Other devices from Arjohuntleigh AB

See all devices from Arjohuntleigh AB →

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 05059441379140|5060693520143VW 61 fields · synced 24 Oct 2026