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Magnoflex

by Orgaterm Produktions- und Warenvertriebsgesellschaft mbH0 6 variants

Ref MA-7004STB/MA-7049GHAModel Augenkompresse/Stirnband

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, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-Magnoflex-1150-4Y9 Basic UDI-DI D-Magnoflex-1150-4Y9UDI-DIDate19 Jul 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

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

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Device Name
Magnoflex Augenkompresse/Stirnband
Model / Reference
Augenkompresse/Stirnband, MA-7004STB/MA-7049GHA
Primary DI / UDI-DI
D-Magnoflex-1150-4Y9
Basic UDI-DI
B-Magnoflex-1150-4Y9
EMDN Code
Z120606 Magnetotherapy equipment
Device Class
Class I
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000035762

Other devices from Orgaterm Produktions- und Warenvertriebsgesellschaft mbH0

Properties

Other properties (11)

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