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Lifemotion Disposable Membrane Oxygenator-500

by Lifemotion Medical Technology Co., Ltd. EUDAMED

Active European Union

Ref LM-BGEA-500Model LM-BGEA-1000, LM-BGEA-500

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number697476268-BGEA-DP Basic UDI-DIDate17 Apr 2025RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED

Device Name
Lifemotion Disposable Membrane Oxygenator
Model / Reference
LM-BGEA-1000, LM-BGEA-500
Primary DI / UDI-DI
06974762682061
Basic UDI-DI
697476268-BGEA-DP
EMDN Code
C03010102 Oxygenator kits
Device Class
Class IIa
Market of Registration
Italy

Manufacturer details

EUDAMED SRN
CN-MF-000043705
Authorised representative
LIFEMOTION S.R.L. IT-AR-000029834

Other devices from Lifemotion Medical Technology Co., Ltd.

See all devices from Lifemotion Medical Technology Co., Ltd. →

Properties

  • Sterile

Other properties (12)

  • 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