Is this your brand? Sign in to claim ownership.

Sign in to claim this brand

Rehatec GmbH

Germany·DE-MF-000006549

Last updated September 18, 2026

About

Rehatec offers stands, inclined loungers, therapy chairs, seat shell underframes and seat shell chassis for children, adolescents and adults with disabilities and a wide variety of needs.

Translated from the manufacturer's own website. Source

What Rehatec GmbH makes

Rehatec GmbH manufactures standing devices, therapy chairs, seat shell underframes, and seat shell chassis for children, adolescents, and adults with disabilities. These products include models such as the Heidelberger Stehgerät Speeedy, Sitzschalenfahrgestell Galileo, Therapiestuhl Nele, Zimmeruntergestell Noah, Sunny Swing, Biometrisches Stehsystem Da Vinci, Heidelberger Liegebär Lasse, Mika, and various configurations of standing and therapy equipment across different sizes and grades.

The devices are classified as Class I medical devices and are listed in the EUDAMED database. The company is based in Germany (DE).

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

Frequently asked questions

What does Rehatec GmbH make?

Rehatec GmbH manufactures standing devices, therapy chairs, seat shell underframes, and seat shell chassis for children, adolescents, and adults with disabilities. Examples include the Heidelberger Stehgerät Speeedy, Sitzschalenfahrgestell Galileo, Therapiestuhl Nele, Zimmeruntergestell Noah, Sunny Swing, Biometrisches Stehsystem Da Vinci, Heidelberger Liegebär Lasse, Mika, and various configurations of standing and therapy equipment across different sizes and grades.

Where is Rehatec GmbH based?

Rehatec GmbH is based in Germany, as indicated by the country code DE in the provided data. This establishes the company’s location within the European Union, which is relevant for regulatory compliance and device listing in EU systems such as EUDAMED.

Which regulatory registry lists Rehatec GmbH’s devices?

Rehatec GmbH’s devices are listed in the EUDAMED database, which is the European Union’s central repository for medical device information under the Medical Devices Regulation (MDR). Listing in EUDAMED indicates that the company has registered its devices in accordance with EU regulatory requirements, though it does not imply device approval or certification.

How are Rehatec GmbH’s devices classified?

Rehatec GmbH’s devices are classified as Class I medical devices. This classification is based on the risk level associated with the devices, with Class I representing the lowest risk category under the EU Medical Devices Regulation. Class I devices are subject to general controls but do not require a notified body assessment for conformity, unless they are sterile or have a measuring function.

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

Information

Country
Germany
Address
35, In den Kreuzwiesen, Schönau, Germany
LinkedIn
—
Phone
+49622891360
PRRC Contact
Christian zu Hohenlohe
EUDAMED SRN
DE-MF-000006549
FDA FEI Number
—
DUNS Number
—

Catalogue (60)

Page 2 of 2
DeviceModel / ReferenceRegistriesClassStatus
Sitzschalenfahrgestell Galileo Gr.1 1023889
EUDAMED
Class IActive
Heidelberger Stehgerät Impuls Gr.2 1023647
EUDAMED
Class IActive
Therapiestuhl Pauli Gr.2 1024058
EUDAMED
Class IActive
Therapiestuhl Nele Classic Gr.0 1010249
EUDAMED
Class IActive
Therapiestuhl Pauli Gr.1 Kiga 1024057
EUDAMED
Class IActive
Heidelberger Liegebär Lasse Gr.4 1007005
EUDAMED
Class IActive
Heidelberger Liegebär Lasse Gr.2 1007955
EUDAMED
Class IActive
Therapiestuhl Pauli Gr.3 1024060
EUDAMED
Class IActive
Zimmeruntergestell Nick Gr.3 1021901
EUDAMED
Class IActive
Heidelberger Stehgerät Benni Light Gr.2 1022840
EUDAMED
Class IActive

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.