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ILUX SMART (open model)

by Mectronic Medicale srl

Ref 10LFModel ILUX LF

ILUX SMART (open model) (10LF) is a Class IIb device made by Mectronic Medicale SRL, registered in EUDAMED on 13 May 2026 (Basic UDI-DI B-08051499970598), active as of 22 Oct 2026.

Active European Union

CE MDD

Valid until

No date given

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

Source EUDAMED, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08051499970598 Basic UDI-DI 08051499970598UDI-DIDate13 May 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Device name
Ilux Lf
Model / reference
ILUX LF, 10LF
Primary DI / UDI-DI
08051499970598
Basic UDI-DI
B-08051499970598
EMDN code
Z120615 Therapeutic lasers
Device class
Class IIb
EU registration type
Legacy device (under a directive)
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000040989

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Properties

Other properties (12, all answered No)