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Plasti-Med

by Plasti-med Plastik Medikal Ürünler San. ve Tic. Ltd. Şti. EUDAMED

Active European Union

Ref 542009

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08699412402094 Basic UDI-DIDate28 Mar 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Expiring

No EU certificate is linked to this device in EUDAMED.

Specification

EUDAMED

Device Name
FASCIAL DILATOR 8 FR 22 cm
Model / Reference
542009
Primary DI / UDI-DI
08699412402094
Basic UDI-DI
B-08699412402094
EMDN Code
L06050101 Non-endoscopic urethral expansion instruments, reusable
Device Class
Class IIa
Market of Registration
Türkiye

Manufacturer details

EUDAMED SRN
TR-MF-000032251

Other devices from Plasti-med Plastik Medikal Ürünler San. ve Tic. Ltd. Şti.

See all devices from Plasti-med Plastik Medikal Ürünler San. ve Tic. Ltd. Şti. →

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