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Oxymag

by Magnamed Tecnologia Medica S/A 2 variants

Ref 1600185

Active European Union

CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-1600185VS Basic UDI-DI D-1600185VSUDI-DIDate13 Jul 2026RegisteredStatusActive

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.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Device Name
Oxymag - Emergency and Transport Ventilator
Model / Reference
1600185
Primary DI / UDI-DI
D-1600185VS
Basic UDI-DI
B-1600185VS
EMDN Code
R9099 Respiratory and anaesthesia devices - other
Device Class
Class IIb
EU market of registration
Türkiye

Manufacturer details

EUDAMED SRN
BR-MF-000013627
Authorised representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Other devices from Magnamed Tecnologia Medica S/A

Properties

  • Administering Medicine

Other properties (10)

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