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Sign in to claim this brandThomas Hilfen für Körperbehinderte GmbH & Co. Medico Kommanditgesellschaft
US
Last updated May 23, 2026
What Thomas Hilfen für Körperbehinderte GmbH & Co. Medico Kommanditgesellschaft makes
Thomas Hilfen für Körperbehinderte produces orthopaedic and foam mattresses designed for medical use, including adjustable sleeping bags and hospital-grade models. Their assistive product line includes manually adjusted ergonomic chairs, pushchairs for mobility support, and child safety seats for vehicles. Additional items include ventilator trays and seat minimizers for wheelchair users.
All listed devices fall under Class I regulatory classification in the US, with product information recorded in the FDA’s Unique Device Identifier (UDI) database. The company operates from the United States, adhering to applicable US medical device regulations.
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 Thomas Hilfen für Körperbehinderte GmbH & Co. Medico Kommanditgesellschaft manufacture?
Thomas Hilfen für Körperbehinderte specializes in assistive and orthopaedic medical devices. Their product line includes orthopaedic and foam mattresses (such as sleeping bags and hospital-grade models), manually adjusted ergonomic chairs, mobility assistive pushchairs, automobile child safety seats, and additional items like ventilator trays and seat minimizers for wheelchair users. These devices are designed to support patients with mobility or comfort needs.
Where is Thomas Hilfen für Körperbehinderte GmbH & Co. Medico Kommanditgesellschaft based?
The company is based in the United States. While the name includes German terms, the business operates within the US regulatory framework, producing devices that comply with applicable US medical device standards.
Which regulatory registries list the devices produced by Thomas Hilfen für Körperbehinderte?
The company’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency of medical devices under US regulatory oversight, allowing healthcare providers and authorities to access standardized product information.
How are the devices manufactured by Thomas Hilfen für Körperbehinderte classified under US regulations?
All listed devices from Thomas Hilfen für Körperbehinderte fall under Class I regulatory classification in the US. This classification applies to low-risk devices, such as mattresses, chairs, and mobility aids, where general controls (like good manufacturing practices) are sufficient for ensuring safety and effectiveness.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
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- FDA FEI Number
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- DUNS Number
- 317356343
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