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Konar-Mf

by LifeTech Scientific (Europe) B.V. Netherlands EUDAMED

Ref LE-MFO-10-8

EMDN P07040301

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08720214000055 Basic UDI-DIDate20 Jul 2023RegisteredStatusActive

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 23 Oct 2026

Device Name
KONAR-MF™ VSD Occluder
Model / Reference
LE-MFO-10-8
Primary DI / UDI-DI
08720214000055
Basic UDI-DI
B-08720214000055
EMDN Code
P07040301 Cardiac occluders, ventricular septal defects
Device Class
Class III
Market of Registration
Croatia

Manufacturer details

EUDAMED SRN
NL-MF-000005742

Other devices from LifeTech Scientific (Europe) B.V.

See all devices from LifeTech Scientific (Europe) B.V. →

Properties & raw data

Show properties, registry sources and raw records
  • Sterile
  • Implantable
Other properties (9)
  • 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 51551f01-ab2a-4c82-bdd1-e56dab287b77 61 fields · synced 23 Oct 2026