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Veolity

EUDAMED

Class IIa (EU MDR)

Ref Veo-2100-CSModel 2.xRef Veo-2000-CS

by MeVis Medical Solutions AG

Identity

Trade Name
Veolity EUDAMED
Device Name
Veolity EUDAMED
Model / Reference
2.x EUDAMED
Veo-2100-CS EUDAMED
Veo-2000-CS EUDAMED

Identifiers

Primary DI / UDI-DI
04260483290237 EUDAMED
04260483290213 EUDAMED
Basic UDI-DI
0426048329VEO35 EUDAMED
Direct Marketing DI
04260483290237 EUDAMED
04260483290213 EUDAMED
EMDN Code
Z11030682 COMPUTED TOMOGRAPHS (CT) - SOFTWARE ACCESSORIES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Special Device Type
Software EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Veolity by Mevis Medical Solutions Ag — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
DE-MF-000005418

Sources (2)

  • EUDAMED 41196f03-73b9-4b3d-8ec7-aadc2b9e41bd 61 fields · synced Jul 29, 2026
  • EUDAMED 98ec4e74-7d7a-492f-8faa-10a7c1ee076d 61 fields · synced May 19, 2026