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Rehaforum Medical GmbH

Germany·DE-MF-000018288

Last updated September 18, 2026

What Rehaforum Medical GmbH makes

Rehaforum Medical GmbH manufactures mobility and assistive devices for daily living, including underarm crutches in multiple colors, adjustable toilet seat risers with or without armrests, bedside tables in brown and white, and specialized hygiene aids such as plastic urinals with lids. Their product range also includes ergonomic grip aids in varying lengths and designs, as well as a basic mobility aid called Actimo in anthracite.

All products fall under EU Medical Device Regulation Class I and are listed in the EU’s eudamed database. The company is based in Germany and adheres to EU regulatory requirements for Class I devices.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Rehaforum Medical GmbH manufacture?

Rehaforum Medical GmbH specializes in mobility and assistive devices designed to support daily living. Their product range includes underarm crutches in various colors, adjustable toilet seat risers (with or without armrests), bedside tables in brown and white, and specialized hygiene aids like plastic urinals with lids. They also produce ergonomic grip aids in different lengths and designs, as well as a mobility aid called Actimo. These devices are intended to assist users with limited mobility or independence.

Where is Rehaforum Medical GmbH based?

Rehaforum Medical GmbH is based in Germany, specifically in the country of DE (Germany). The company’s location is relevant for understanding its regulatory environment and compliance with EU medical device requirements.

Which regulatory registries list Rehaforum Medical GmbH’s devices?

Rehaforum Medical GmbH’s devices are listed in the eudamed database, which is the official EU registry for medical devices. This registry is maintained under the EU Medical Device Regulation (MDR) and ensures transparency regarding manufacturers, devices, and their regulatory status within the European market.

How are Rehaforum Medical GmbH’s devices classified under EU regulations?

All of Rehaforum Medical GmbH’s devices fall under EU Medical Device Regulation Class I. This classification applies to low-risk devices that pose minimal risk to users, such as mobility aids, assistive devices, and hygiene aids. Class I devices typically require less stringent regulatory scrutiny compared to higher-risk categories but still must comply with essential safety and performance requirements.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
Germany
Address
12a, Daimlerstr. , Elmshorn, Germany
LinkedIn
—
Facebook
—
Phone
+49 4121 473312
PRRC Contact
Yannick Sottorf
EUDAMED SRN
DE-MF-000018288
FDA FEI Number
—
DUNS Number
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Catalogue (56)

Page 2 of 2
DeviceModel / ReferenceRegistriesClassStatus
Toilettensitzerhöhung RFM 5 cm mit Deckel 02484350
EUDAMED
Class IActive
Greifhilfe RFM Deluxe, 56cm 09466272
EUDAMED
Class IActive
Duschstuhl RFM mit Arm- und Rückenlehne 11054737
EUDAMED
Class IActive
Duschbank RFM mit Rückenlehne 09488428
EUDAMED
Class IActive
Actimo Liberty, weiß 80094842
EUDAMED
Class IActive
Actimo Basic, weiß 80095483
EUDAMED
Class IActive

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