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Station d’accueil batterie Vendom

by Air Liquide Medical Systems S.A. EUDAMED

Withdrawn No longer placed on the EU market

Ref KC042300

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number37005043VENDOM_BATTERY4K Basic UDI-DIDate7 Oct 2021RegisteredStatusWithdrawn No longer placed on the EU market

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Withdrawn

Certificates

0 certificates · EUDAMED

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

Specification

EUDAMED

Device Name
Station d’accueil batterie Vendom
Model / Reference
KC042300
Primary DI / UDI-DI
03700504300633
Basic UDI-DI
37005043VENDOM_BATTERY4K
Direct Marketing DI
03700504300633
EMDN Code
Z1203019080 Various instruments for anaesthesia and pulmonary ventilation support - hardware accessories
Device Class
Class I
Market of Registration
France

Manufacturer details

EUDAMED SRN
FR-MF-000003649

Other devices from Air Liquide Medical Systems S.A.

See all devices from Air Liquide Medical Systems S.A. →

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