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Xo O2 200B 25E Ol Sis 15l

by Air Liquide Medical Systems S.A. EUDAMED

Withdrawn Not intended for the EU market

Ref CK062543Model XO / XO SMART

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number37005043XO7A Basic UDI-DIDate18 Jun 2025RegisteredStatusWithdrawn Not intended for 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  • Withdrawn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European Union — CE/MDR Withdrawn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

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Specification

EUDAMED

Device Name
Xo / Xo Smart
Model / Reference
XO / XO SMART, CK062543
Primary DI / UDI-DI
03700504301241
Basic UDI-DI
37005043XO7A
Direct Marketing DI
03700504301241
EMDN Code
Z120309 Medical/medicinal gas pipeline systems and related accessories
Device Class
Class IIb

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

  • CMR Substance
  • Administering Medicine

Other properties (11)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No