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lifecath biflux

by VYGON Germany GmbH 5 variants

Ref 2293.090

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-03660812127110 Basic UDI-DI 03660812127110UDI-DIDate21 Jul 2026RegisteredStatusActive

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

GermanyFranceTürkiyeGreece
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDD Active

  • France
  • Germany
  • Greece
  • Türkiye

Specification

EUDAMED

Model / Reference
2293.090
Primary DI / UDI-DI
03660812127110
Basic UDI-DI
B-03660812127110
EMDN Code
C01020302 Central venous double-lumen catheters, partially tunneled
Device Class
Class III
EU market of registration
France

Manufacturer details

EUDAMED SRN
DE-MF-000005305

Other devices from VYGON Germany GmbH

See all devices from VYGON Germany GmbH →

Properties

  • Sterile
  • Implantable

Other properties (9)

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