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MultiCath 4J Sp ø5F 2-5-2mm

by VascoMed GmbH EUDAMED

Active European Union

Ref 351171

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number426009092BUDI00012FD Basic UDI-DIDate27 Aug 2026RegisteredStatusActive

Coverage

1 jurisdiction

NorwayIcelandSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaLiechtensteinAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyTürkiyeCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Map note: Northern Ireland has no dot of its own.

  • Austria
  • Belgium
  • Bulgaria
  • Croatia
  • Cyprus
  • Czechia
  • Denmark
  • Estonia
  • Finland
  • France
  • Germany
  • Greece
  • Hungary
  • Iceland
  • Ireland
  • Italy
  • Latvia
  • Liechtenstein
  • Lithuania
  • Luxembourg
  • Malta
  • Netherlands
  • Northern Ireland
  • Norway
  • Poland
  • Portugal
  • Romania
  • Slovakia
  • Slovenia
  • Spain
  • Sweden
  • Türkiye

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • 20375GB450250730 Active

    Technical documentation EU MDR

    Notified body
    0482
    Issued
    30 Jul 2025
    Expires
    29 Jul 2030

Specification

EUDAMED

Device Name
MultiCath
Model / Reference
351171
Primary DI / UDI-DI
04251883700686
Basic UDI-DI
426009092BUDI00012FD
EMDN Code
C02010401 Arrhythmology multipolar diagnostic catheters, conventional
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