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Actimo Basic XXL

EUDAMED

Class I (EU MDR)

Ref 05374739

by Rehaforum Medical GmbH

Identity

Trade Name
Actimo Basic XXL EUDAMED
Device Name
Actimo Basic XXL EUDAMED
Model / Reference
05374739 EUDAMED

Identifiers

Primary DI / UDI-DI
04041314026313 EUDAMED
Basic UDI-DI
4041314actimobasicxxl6C EUDAMED
Direct Marketing DI
04041314026313 EUDAMED
EMDN Code
Y120615 POWER ASSISTED MOBILITY ROLLATORS 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

Actimo Basic XXL by Rehaforum Medical 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-000018288

Sources (1)

  • EUDAMED cc0a943f-e55c-490c-8cb4-1fbcf43776ee 61 fields · synced Jun 20, 2026