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H-Ekg 1080/Ee 850

EUDAMED

Class I (EU MDR)

Ref 59Model H-EKG 1080/EE 850

by AGA Sanitätsartikel GmbH

Identity

Trade Name
H-EKG 1080/EE 850 EUDAMED
Device Name
Liege EUDAMED
Model / Reference
H-EKG 1080/EE 850 EUDAMED
59 EUDAMED

Identifiers

Primary DI / UDI-DI
04251816801664 EUDAMED
Basic UDI-DI
4251816801669Q EUDAMED
Direct Marketing DI
04251816801664 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

H-Ekg 1080/Ee 850 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 198ba5cb-4c62-41cd-bcf7-0d6b1a40f080 61 fields · synced Jun 20, 2026