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Vanguard Irrigated Ablation Catheter SF NAV bi ST BWY DF-Type 8F 115cm 6p 1-6-2 TC TE3.5

by Vanguard AG

Ref 35132Model DF-Type 8F 115cm 6p 1-6-2 TC TE3.5

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-35132G4 Basic UDI-DI D-35132G4UDI-DIDate29 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

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Device Name
Vanguard Irrigated Ablation Catheter SF NAV bi ST BWY
Model / Reference
DF-Type 8F 115cm 6p 1-6-2 TC TE3.5, 35132
Primary DI / UDI-DI
D-35132G4
Basic UDI-DI
B-35132G4
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