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TricValve® Transcatheter Bicaval Valve System - IVC 35

by P+F Products and Features GmbH

Ref PF01020035Model TricValve® Transcatheter Bicaval Valve System

Active European Union

CE MDR

Valid until

5 Feb 2031

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier POLSKIE CENTRUM BADAN I CERTYFIKACJI S.A.

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number426064234TricValveBM Basic UDI-DI 04260642340032UDI-DIDate12 Feb 2026RegisteredStatusActive

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Model / Reference
TricValve® Transcatheter Bicaval Valve System, PF01020035
Primary DI / UDI-DI
04260642340032
Basic UDI-DI
426064234TricValveBM
EMDN Code
P07030104 Biological valves, bicaval
Device Class
Class III
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000008580

Other devices from P+F Products and Features GmbH

Properties

  • Sterile
  • Implantable
  • Animal Tissues

Other properties (10)

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