TZM GmbH
Germany DE-MF-000006349 Last updated 23 May 2026
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- Devices
- 1
- Registries
- EUDAMED
- FDA recalls
- 0
Catalogue
Umg Ref 101001
What TZM GmbH makes
TZM GmbH manufactures the UMG, a medical device designed for monitoring and recording physiological signals, including electrocardiograms (ECG), blood pressure, and other vital parameters in clinical and research settings. The device is intended for use in hospitals, laboratories, and intensive care environments to support patient diagnostics and continuous monitoring.
The UMG falls under EU medical device classification as Class IIb, requiring compliance with stringent regulatory requirements under the Medical Device Regulation (MDR). It is registered in the EU’s eudamed database, ensuring traceability and transparency for regulatory oversight. The company is based in Germany.
Frequently asked questions
What types of medical devices does TZM GmbH manufacture?
TZM GmbH specializes in the UMG, a medical device designed for monitoring and recording physiological signals such as electrocardiograms (ECG), blood pressure, and other vital parameters. This device is primarily used in clinical and research settings, including hospitals, laboratories, and intensive care units, to aid in patient diagnostics and continuous monitoring.
Where is TZM GmbH based?
TZM GmbH is based in Germany, operating from a location within the country. The company’s headquarters or primary operational address is located in DE, as indicated by its registration details.
Which regulatory registries list TZM GmbH’s devices?
TZM GmbH’s devices, including the UMG, are listed in the eudamed database, which is the EU’s central registry for medical devices. This registration ensures traceability and compliance with EU regulatory requirements, particularly under the Medical Device Regulation (MDR).
How are TZM GmbH’s devices classified under EU regulations?
The UMG falls under Class IIb classification in the EU’s medical device regulatory framework. This classification is assigned based on the device’s intended purpose and associated risks, requiring compliance with stricter regulatory controls, such as clinical evaluations and conformity assessments, to ensure safety and performance.
Information
- Country
- Germany
- Address
- 41, Davidstraße, Goeppingen, Germany
- Website
- tzm.de/umg
- [email protected]
- Phone
- +49 7161 5023-200
- PRRC contact
- Isabel Böhringer
- EUDAMED SRN
- DE-MF-000006349