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AlCath Flutter Black LT G

by VascoMed GmbH EUDAMED

Active European Union

Ref 368997

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number426009092BUDI00001F8 Basic UDI-DIDate2 Sep 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • 20374GB450260819 Active Supplemented

    Technical documentation EU MDR

    Notified body
    0482
    Issued
    19 Aug 2026
    Expires
    21 Dec 2030
    Reason
    Change approved

Specification

EUDAMED

Device Name
AlCath
Model / Reference
368997
Primary DI / UDI-DI
04251883700488
Basic UDI-DI
426009092BUDI00001F8
EMDN Code
C020301 Arrhythmogenic foci radiofrequency ablation catheters
Device Class
Class III
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000005571

Other devices from VascoMed GmbH

See all devices from VascoMed GmbH →

Properties

  • Sterile

Other properties (12)

  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No