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ReOxy

by Bitmos GmbH EUDAMED

Active European Union

Ref 60-2001 EUModel ReOxy EU

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-04260159850208 Basic UDI-DIDate21 Oct 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDD Active

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

Model / Reference
ReOxy EU, 60-2001 EU
Primary DI / UDI-DI
04260159850208
Basic UDI-DI
B-04260159850208
EMDN Code
R9099 Respiratory and anaesthesia devices - other
Device Class
Class IIb
Market of Registration
Luxembourg

Manufacturer details

EUDAMED SRN
DE-MF-000005034

Other devices from Bitmos GmbH

Properties

  • Administering Medicine
  • Measuring Function

Other properties (9)

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