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Eka-1080

EUDAMED

Class I (EU MDR)

Ref 64Model EKA-1080

by AGA Sanitätsartikel GmbH

Identity

Trade Name
EKA-1080 EUDAMED
Device Name
Liege EUDAMED
Model / Reference
EKA-1080 EUDAMED
64 EUDAMED

Identifiers

Primary DI / UDI-DI
04251816801732 EUDAMED
Basic UDI-DI
4251816801739M EUDAMED
Direct Marketing DI
04251816801732 EUDAMED
EMDN Code
V080699 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

Eka-1080 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 14f8ce00-3351-41a7-9790-9208be1b8c61 61 fields · synced Oct 5, 2026