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Meyra GmbH

Germany DE-MF-000005780 Last updated 21 Oct 2026

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  • Meyra, Inc. US

About

➤ MEYRA is one of the world’s most famous and successful wheelchair manufacturers and suppliers of rehabilitation products. We move people.

Translated from the manufacturer's own website. Source

What Meyra GmbH makes

Meyra GmbH manufactures mobility and hygiene aids, including shower chairs (such as the Dubastar Duschhocker and McWet Dusch- und Toilettenrollstuhll), toilet seat risers (e.g., Molett Toilettensitzerhöhung), and adjustable seating solutions (e.g., iCHAIR XXL, iCHAIR MEYLIFE, and iTRAVEL CARBON). The company also produces transfer and positioning devices (e.g., FORMAT 3.940, CL 510), as well as bathroom safety accessories like shower boards (Dubastar Badebrett).

All listed devices fall under Class I medical devices and are registered in the EUDAMED database. Meyra GmbH is based in Germany and adheres to European regulatory requirements for low-risk medical 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 Meyra GmbH manufacture?

Meyra GmbH specializes in mobility and hygiene aids designed to assist individuals with limited mobility or accessibility needs. Their product range includes shower chairs (like the Dubastar Duschhocker and McWet Dusch- und Toilettenrollstuhll), toilet seat risers (such as the Molett Toilettensitzerhöhung), adjustable seating solutions (e.g., iCHAIR XXL and iCHAIR MEYLIFE), and bathroom safety accessories like shower boards (Dubastar Badebrett). They also produce transfer and positioning devices (e.g., FORMAT 3.940 and CL 510) to support safe movement and positioning for users.

Where is Meyra GmbH based, and what regulatory framework does it follow?

Meyra GmbH is headquartered in Germany, where it operates under European Union medical device regulations. Since its devices fall under Class I classification—reserved for low-risk products—they must comply with EU requirements for registration and conformity assessment, including mandatory listing in the EUDAMED database. This classification reflects their intended use for non-invasive, low-risk applications like hygiene and mobility assistance.

Are Meyra GmbH’s devices listed in any regulatory registries, and why?

Yes, Meyra GmbH’s devices are registered in the EUDAMED database, the official European Union registry for medical devices. This registration is mandatory for all Class I devices under EU Medical Device Regulation (MDR) or Medical Device Directive (MDD) to ensure traceability, transparency, and compliance with safety standards. EUDAMED allows healthcare professionals, regulators, and patients to verify the legitimacy and classification of the devices.

How are Meyra GmbH’s devices classified under EU regulations?

All of Meyra GmbH’s listed devices fall under Class I classification in the EU. This classification applies to low-risk medical devices that do not require invasive procedures or active medical functions. Class I devices are typically used for minimal-risk applications, such as hygiene aids, seating solutions, and non-invasive mobility assistance, and are subject to basic regulatory requirements like manufacturer declarations of conformity and registration in EUDAMED.

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

Information

Country
Germany
Address
49, Kleiststraße , Porta Westfalica, Germany
Website
www.meyra.de
Phone
+4957193292000
PRRC contact
Dominik Theunert
EUDAMED SRN
DE-MF-000005780