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Vanguard Steerable Diagnostic Catheter ID BWAB F-Type 6F 115cm 10p 2-8-2

by Vanguard AG

Ref 35050Model F-Type 6F 115cm 10p 2-8-2

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-35050FZ Basic UDI-DI D-35050FZUDI-DIDate24 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  • Withdrawn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 Steerable Diagnostic Catheter ID BWAB
Model / Reference
F-Type 6F 115cm 10p 2-8-2, 35050
Primary DI / UDI-DI
D-35050FZ
Basic UDI-DI
B-35050FZ
EMDN Code
C02010403 Arrhythmology multipolar diagnostic catheters, adjustable
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