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Optico Ltd

by Optico Ltd EUDAMED

Active European Union

Ref 30-208

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-05060326003067 Basic UDI-DIDate28 Sep 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDD Expiring

Certificates

0 certificates · EUDAMED

No notified-body certificate is listed. Devices of this class are self-declared by the manufacturer.

Specification

EUDAMED

Device Name
Double End Nucleus Divider / Phaco Spatula Blunt
Model / Reference
30-208
Primary DI / UDI-DI
05060326003067
Basic UDI-DI
B-05060326003067
EMDN Code
L1705 Ophthalmology probes, reusable
Device Class
Class I
Market of Registration
Netherlands

Manufacturer details

EUDAMED SRN
GB-MF-000031949
Authorised representative
Advena Limited MT-AR-000000234

Other devices from Optico Ltd

See all devices from Optico Ltd →

Properties

  • Reusable

Other properties (10)

  • Sterile: No
  • Implantable: 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