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Veko-1060/Ee

EUDAMED

Class I (EU MDR)

Ref 37Model VEKO-1060/EE

by AGA Sanitätsartikel GmbH

Identity

Trade Name
VEKO-1060/EE EUDAMED
Device Name
Phlebologieliege EUDAMED
Model / Reference
VEKO-1060/EE EUDAMED
37 EUDAMED

Identifiers

Primary DI / UDI-DI
04251816800414 EUDAMED
Basic UDI-DI
42518168004193 EUDAMED
Direct Marketing DI
04251816800414 EUDAMED
EMDN Code
V08060199 ELECTRIC MEDICAL BEDS - OTHER EUDAMED

Classification

Device Class
Class I 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

Veko-1060/Ee by AGA Sanitätsartikel GmbH — Class I — 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-000005876

Sources (1)

  • EUDAMED 93059aab-e2d6-4428-818f-f3d87455750c 61 fields · synced Oct 6, 2026