Dr. Müller Gerätebau GmbH
Germany DE-MF-000024467 Last updated 17 Sep 2026
- Devices
- 4
- Registries
- EUDAMED
- FDA recalls
- 0
Catalogue
Super Gl 2 Ref 053000000000
SensoStar GL30 touch Ref 920118
SensoStar GLH six Ref 920800
SUPER GL compact Ref 0540 000 000
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.
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.
Information
- Country
- Germany
- Address
- 133, Burgker Str., Freital, Germany
- Website
- dr-mueller-geraetebau.de
- [email protected]
- PRRC contact
- Matthias Hartwig
- EUDAMED SRN
- DE-MF-000024467