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Vidi Medikal Teknik

by Vi̇di̇ Medi̇kal Tekni̇k Veysel Özkapici Ve Kurtuluş Özkapici Kollekti̇f Şi̇rketi̇ EUDAMED

Active European Union

Ref C-243Model Backflush Instrument 25G Ext.Silicone Active Aspiration

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08683318132438 Basic UDI-DIDate11 Sep 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Expiring

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.

Specification

EUDAMED

Device Name
Backflush Instrument 25G Ext.Silicone Active Aspiration
Model / Reference
Backflush Instrument 25G Ext.Silicone Active Aspiration, C-243
Primary DI / UDI-DI
08683318132438
Basic UDI-DI
B-08683318132438
EMDN Code
Q021199 Ophthalmic surgery instruments, single-use - other
Device Class
Class IIa
Market of Registration
Italy

Manufacturer details

EUDAMED SRN
TR-MF-000027806

Other devices from Vi̇di̇ Medi̇kal Tekni̇k Veysel Özkapici Ve Kurtuluş Özkapici Kollekti̇f Şi̇rketi̇

See all devices from Vi̇di̇ Medi̇kal Tekni̇k Veysel Özkapici Ve Kurtuluş Özkapici Kollekti̇f Şi̇rketi̇ →

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