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CeraFlex

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

Ref LE-ASDf-08

EMDN P07040302

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-08720214005357 Basic UDI-DIDate2 Aug 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 22 Oct 2026

Device Name
CeraFlex™ ASD Closure System
Model / Reference
LE-ASDf-08
Primary DI / UDI-DI
08720214005357
Basic UDI-DI
B-08720214005357
EMDN Code
P07040302 Cardiac occluders, atrial septal defects
Device Class
Class III
Market of Registration
Austria

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
  • Implantable
  • Contains Latex
Other properties (9)
  • Sterile: No
  • Reusable: 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 cca3457c-f970-4334-b54e-b18a5da1e41a 61 fields · synced 22 Oct 2026