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Floh HB

EUDAMED

Class I (EU MDR)

Ref M800

by Berollka-aktiv Rollstuhltechnik GmbH

Identity

Trade Name
Floh HB EUDAMED
Device Name
Floh HB EUDAMED
Model / Reference
M800 EUDAMED

Identifiers

Primary DI / UDI-DI
04066358200253 EUDAMED
Basic UDI-DI
40663582010M8000000LG EUDAMED
Direct Marketing DI
04066358200253 EUDAMED
EMDN Code
Y180939 MODULAR POSTURE SYSTEMS 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

Floh HB by Berollka-aktiv Rollstuhltechnik 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-000007043

Sources (1)

  • EUDAMED e0a5ed07-2277-4374-b430-1bfc1dc6273f 61 fields · synced Oct 6, 2026