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Optofresh Multipurpose Solution

by Ioulia and Irene Tseti Pharmaceutical Laboratories S.A.

Ref OPTOFRESH MULTIPURPOSE SOLUTION

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 26 Oct 2026. What this means

Regulatory status

as of registry sync 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-OPTOMD2203XU Basic UDI-DI D-OPTOMD2203XUUDI-DIDate13 Dec 2023RegisteredStatusActive

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  • Withdrawn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

Model / Reference
OPTOFRESH MULTIPURPOSE SOLUTION
Primary DI / UDI-DI
D-OPTOMD2203XU
Basic UDI-DI
B-OPTOMD2203XU
EMDN Code
Q02030204 Contact lenses storing and cleaning solutions
Device Class
Class IIb
EU market of registration
Greece

Manufacturer details

EUDAMED SRN
GR-MF-000032958

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Properties

  • Sterile

Other properties (10)

  • 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