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Sign in to claim this brandRehatec 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
- Website
- www.rehatec.com
- —
- facebook.com/rehatec
- [email protected]
- Phone
- +49622891360
- PRRC Contact
- Christian zu Hohenlohe
- EUDAMED SRN
- DE-MF-000006549
- FDA FEI Number
- —
- DUNS Number
- —
Catalogue (60)
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