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Optofresh Ecto

by Ioulia and Irene Tseti Pharmaceutical Laboratories S.A.

Ref OPTOFRESH ECTO

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-OPTOMD2301XV Basic UDI-DI D-OPTOMD2301XVUDI-DIDate12 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  • Withdrawn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 ECTO
Primary DI / UDI-DI
D-OPTOMD2301XV
Basic UDI-DI
B-OPTOMD2301XV
EMDN Code
Q0299 Ophthalmic devices - other
Device Class
Class IIb
EU market of registration
Greece

Manufacturer details

EUDAMED SRN
GR-MF-000032958

Other devices from Ioulia and Irene Tseti Pharmaceutical Laboratories S.A.

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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