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Rgl-1080/Kee

EUDAMED

Class I (EU MDR)

Ref 24Model RGL-1080/KEE

by AGA Sanitätsartikel GmbH

Identity

Trade Name
RGL-1080/KEE EUDAMED
Device Name
Liege EUDAMED
Model / Reference
RGL-1080/KEE EUDAMED
24 EUDAMED

Identifiers

Primary DI / UDI-DI
04251816800209 EUDAMED
Basic UDI-DI
4251816800208T EUDAMED
Direct Marketing DI
04251816800209 EUDAMED
EMDN Code
V080603 TREATMENT, DIAGNOSIS AND MONITORING MEDICAL BEDS 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

Rgl-1080/Kee 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 48a0c762-66cd-45c7-b87d-bfdd9b9e2a48 61 fields · synced Oct 6, 2026