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Meibomask

by Espansione Marketing SpA 8 variants

Ref MEIBOMASK/PS

MEIBOMASK/PS is a medical device (EU MDD Class IIa) made by Espansione Marketing SpA, registered in EUDAMED on 23 Jun 2026 (Basic UDI-DI 80563897MEIBOMASKD004E), active as of 23 Oct 2026.

Active European Union

CE MDR 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD Number80563897MEIBOMASKD004E Basic UDI-DI Date23 Jun 2026RegisteredStatusActive
European UnionCE/MDR Number80563897MEIBOMASKD004E Basic UDI-DI Date23 Jun 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD, CE/MDR Active

Specification

EUDAMED

Device name
Device for phototherapy in ophthalmology
"Devices with LED light technology (LLLT) for professional use in Ophthalmology"
Model / reference
MEIBOMASK/PS
Primary DI / UDI-DI
08056389703003, 08056389700484
Basic UDI-DI
80563897MEIBOMASKD004E, B-08056389700484
EMDN code
Z12120299, Z12120199
Device class
Class IIa
EU registration type
Standard device
Legacy device (under a directive)
EU market of registration
Greece
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000027514

Similar devices in this category

Other devices filed under OPHTALMOLOGY ASSESSMENTS AND DIAGNOSIS INSTRUMENTS – OTHER.

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Properties

Other properties (14, all answered No)