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Vanguard Ablation Catheter uni BWA D-Type 7F 115cm 4p 2-5-2 TR

by Vanguard AG

Ref 33497Model D-Type 7F 115cm 4p 2-5-2 TR

Active European Union

CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-33497GZ Basic UDI-DI D-33497GZUDI-DIDate18 Sep 2025RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

DenmarkGermanyFranceBelgium
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDD Active

  • Belgium
  • Denmark
  • France
  • Germany

Specification

EUDAMED

Device Name
Vanguard Ablation Catheter uni BWA
Model / Reference
D-Type 7F 115cm 4p 2-5-2 TR, 33497
Primary DI / UDI-DI
D-33497GZ
Basic UDI-DI
B-33497GZ
EMDN Code
C020301 Arrhythmogenic foci radiofrequency ablation catheters
Device Class
Class III
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000006091

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Properties

  • Sterile
  • Reprocessed

Other properties (9)

  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No