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Vojta/Bobath Maxi-EL

EUDAMED

Class I (EU MDR)

Ref K101 BEKA Pflege- und Versorgungsliegen und deren Zubehöre

by BEKA-Hospitec GmbH

Identity

Trade Name
Vojta/Bobath Maxi-EL EUDAMED
Device Name
Manipulat 2-HYD EUDAMED
Model / Reference
K101 BEKA Pflege- und Versorgungsliegen und deren Zubehöre EUDAMED

Identifiers

Primary DI / UDI-DI
04260735022074 EUDAMED
Basic UDI-DI
426068189101BH EUDAMED
Direct Marketing DI
04260735022074 EUDAMED
EMDN Code
Y1803 ASSISTIVE TABLES 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

Vojta/Bobath Maxi-EL by BEKA Hospitec 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

Manufacturer
BEKA-Hospitec GmbH
EUDAMED SRN
DE-MF-000013895

Sources (1)

  • EUDAMED 50251531-dea2-4a99-9905-9a493d853f82 61 fields · synced Aug 4, 2026