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pRESET LITE Thrombectomy Device

by phenox Ltd Ireland EUDAMED

Ref IE102042011Model pRESET LITE Thrombectomy Device 4mmx20mm

EMDN C010404020401

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-05391530910118 Basic UDI-DIDate6 Jul 2026RegisteredStatusWithdrawn No longer placed on the EU market

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Withdrawn
  • Not covered

European Union — CE/MDD Withdrawn

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 24 Oct 2026

Model / Reference
pRESET LITE Thrombectomy Device 4mmx20mm, IE102042011
Primary DI / UDI-DI
05391530910118
Basic UDI-DI
B-05391530910118
EMDN Code
C010404020401 Manual neurovascular thrombectomy and thromboaspiration systems
Device Class
Class III

Manufacturer details

EUDAMED SRN
IE-MF-000011333

Other devices from Phenox Limited

See all devices from Phenox Limited →

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 05391530910118|B-05391530910118 61 fields · synced 24 Oct 2026