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SCHMITZ medical GmbH

US

Last updated May 31, 2026

Part of SCHMITZ medical GmbH

What SCHMITZ medical GmbH makes

SCHMITZ medical GmbH manufactures electric general examination and treatment chairs designed for clinical use. These devices are intended for patient positioning and support during medical procedures, examinations, or treatments in healthcare settings.

The company’s portfolio is classified under FDA’s Class I medical devices and is listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer is based in the United States.

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 SCHMITZ medical GmbH manufacture?

SCHMITZ medical GmbH specializes in producing electric general examination and treatment chairs. These devices are designed for clinical use to provide patient positioning and support during medical procedures, examinations, or treatments in healthcare environments. Their focus is on creating equipment that aids in patient care within medical settings.

Where is SCHMITZ medical GmbH based?

SCHMITZ medical GmbH is based in the United States. The company’s headquarters and operations are located within the country, though specific regional offices or manufacturing sites may vary.

Which regulatory registries or databases list SCHMITZ medical GmbH’s devices?

SCHMITZ medical GmbH’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify medical devices authorized for use in the United States, ensuring transparency and traceability for healthcare providers and regulators.

How are SCHMITZ medical GmbH’s devices classified by regulatory authorities?

SCHMITZ medical GmbH’s devices fall under the FDA’s Class I classification. Class I devices are generally considered to pose the lowest risk and often include items like examination chairs, where the risk of illness or injury from misuse is minimal. This classification is determined based on the device’s intended use and potential risks.

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

Information

Country
US
Address
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Website
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LinkedIn
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Facebook
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Email
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Phone
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PRRC Contact
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EUDAMED SRN
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FDA FEI Number
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DUNS Number
316025501

Catalogue (4)

DeviceModel / ReferenceRegistriesClassStatus
Schmitz arco-matic 200 M
FDA UDI
Class IActive
Schmitz medi-matic 115.9
EUDAMEDFDA UDI
Class IActive
Schmitz arco-matic 300 M
FDA UDI
Class IActive
Schmitz arco-matic URO
FDA UDI
Class IActive

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