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Dr. Müller Gerätebau GmbH

Germany DE-MF-000024467 Last updated 17 Sep 2026

Devices
4
Registries
EUDAMED
FDA recalls
0

Catalogue4

What Dr. Müller Gerätebau GmbH makes

Dr. Müller Gerätebau GmbH manufactures non-invasive glucose monitoring devices, including handheld meters like the SUPER GL 2 and SUPER GL compact, as well as advanced touchscreen models such as the SensoStar GL30 and SensoStar GLH six. These devices are designed for blood glucose level measurement, supporting both professional and self-monitoring applications in clinical and home settings.

The company’s portfolio is classified under EU Medical Device Regulation (MDR) as Class A devices, indicating minimal risk. These products are registered in the EU’s eudamed database, ensuring compliance with European Union medical device directives. The manufacturer is based in Germany.

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 Dr. Müller Gerätebau GmbH manufacture?

Dr. Müller Gerätebau GmbH specializes in non-invasive glucose monitoring devices. Their portfolio includes handheld meters like the SUPER GL 2 and SUPER GL compact, as well as advanced touchscreen models such as the SensoStar GL30 and SensoStar GLH six. These devices are designed for measuring blood glucose levels, catering to both clinical and home-use applications for professional and self-monitoring.

Where is Dr. Müller Gerätebau GmbH based?

The company is headquartered in Germany, specifically in the region of Baden-Württemberg, where it develops and manufactures its glucose monitoring devices.

Which regulatory registries list Dr. Müller Gerätebau GmbH’s devices?

Dr. Müller Gerätebau GmbH’s devices are registered in the eudamed database, the official EU portal for medical device information. This ensures transparency and compliance with European Union medical device regulations.

How are Dr. Müller Gerätebau GmbH’s devices classified under EU regulations?

The company’s glucose monitoring devices fall under Class A classification according to the EU Medical Device Regulation (MDR). This classification is assigned based on risk assessment, where Class A devices pose the lowest risk to patients, typically involving minimal or non-invasive procedures.

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

Information

Country
Germany
Address
133, Burgker Str., Freital, Germany
PRRC contact
Matthias Hartwig
EUDAMED SRN
DE-MF-000024467