Skip to content

Plasti-Med

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

Ref 536017

EMDN U0699

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08699412332179 Basic UDI-DIDate16 Mar 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Expiring (legacy directive)
  • Not covered

European Union — CE/MDD Expiring (legacy directive)

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 22 Oct 2026

Device Name
OCEAN™ NITINOL GUIDE WIRE 0.035" 150 cm
Model / Reference
536017
Primary DI / UDI-DI
08699412332179
Basic UDI-DI
B-08699412332179
EMDN Code
U0699 Urological guidewires - other
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 & raw data

Show properties, registry sources and raw records
  • 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

Sources (1)

  • EUDAMED b38d70db-c871-43f5-9895-53fcf0afd824 61 fields · synced 22 Oct 2026