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Vitus

EUDAMED

Class III (EU MDR)

Ref VIT0300060150

by eucatech AG

Identity

Trade Name
VITUS EUDAMED
Device Name
VITUS Paclitaxel Coated PTA Catheter EUDAMED
Model / Reference
VIT0300060150 EUDAMED

Identifiers

Primary DI / UDI-DI
04251895630810 EUDAMED
Basic UDI-DI
B-04251895630810 EUDAMED
EMDN Code
C010402020101 PTA BALLOON DILATATION CATHETERS EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

Yes

EUDAMED

Vitus by eucatech AG — Class III — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

Manufacturer
eucatech AG
EUDAMED SRN
DE-MF-000005541

Sources (1)

  • EUDAMED a51c8750-c758-4b23-9d5b-04911b8c3586 61 fields · synced Jun 18, 2026