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Lumina 3D-e FDC EA

by Karel Hrnčíř - BIOMAG

Ref Lumina 3D-e FDC EA

Active European Union

CE MDR

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number859420828SYSTEMLUMINA3B2 Basic UDI-DI 08594208287377UDI-DIDate26 Jun 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  • Withdrawn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/MDR Active

Specification

EUDAMED

Device Name
Set BIOMAG® Lumina 3D-e
Model / Reference
Lumina 3D-e FDC EA
Primary DI / UDI-DI
08594208287377
Basic UDI-DI
859420828SYSTEMLUMINA3B2
EMDN Code
Z120606 Magnetotherapy equipment
Device Class
Class IIa
Medical Purpose
Set BIOMAG® Lumina 3D-e je určen k doplňkové symptomatické léčbě pro podporu mírnění bolestí, otoků, křečí a detoxikaci, pro zlepšení prokrvení (vasodilatace) a urychlení hojení.

Manufacturer details

EUDAMED SRN
CZ-PR-000056217

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Properties

Other properties (1)

  • Sterile: No