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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Organization name
UDI-DI code
Reference / catalog number

09509018 — Class I MDR by Rehaforum Medical GmbH

MD Atlas
Rehaforum Medical GmbH

EUDAMED last updated this device on Jul 18, 2025

09509018

4041314actimohomeSG

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Rehaforum Medical GmbH
UDI-DI code: 04041314031300
Reference / catalog number: 09509018

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Manufacturer information

Organization name: Rehaforum Medical GmbH
SRN: DE-MF-000018288
Manufacturer status: Active

Market distribution

Primary placement in Germany; available across 1 country total.

Placed on the market in Germany; per-country availability dates not published.

Device identification

Trade name: not provided
UDI-DI code: 04041314031300
Basic UDI-DI: 4041314actimohomeSG
Reference / catalog number: 09509018
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Der Rollator dient zur Unterstützung des Gehens und zur Erhaltung der Aktivität von Personen, die in ihrer Mobilität eingeschränkt sind. Der Rollator ist ausschließlich für die Nutzung im Innenbereich bestimmt.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Y120606WHEELED WALKER

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

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Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.