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Vitus

by eucatech AG 28 variants

Ref VIT0700150085

Vitus (VIT0700150085) is a Class III device made by eucatech AG, registered in EUDAMED on 31 May 2024 (Basic UDI-DI B-04251895630698), active as of 24 Oct 2026.

Active European Union

CE MDD

Valid until

No date given

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

Source EUDAMED, synced 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-04251895630698 Basic UDI-DI 04251895630698UDI-DIDate31 May 2024RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Device name
VITUS Paclitaxel Coated PTA Catheter
Model / reference
VIT0700150085
Primary DI / UDI-DI
04251895630698
Basic UDI-DI
B-04251895630698
EMDN code
C010402020101 PTA balloon dilatation catheters
Device class
Class III
EU registration type
Legacy device (under a directive)
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000005541

Related devices

Category: Peripheral angioplasty balloon catheter, basic

Similar devices in this category

Other devices filed under PTA BALLOON DILATATION CATHETERS.

Other devices from eucatech AG

See all devices from eucatech AG →

Properties

  • Supplied sterile
  • Incorporates a medicinal substance
Other properties (10, all answered No)