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TZM GmbH

Germany DE-MF-000006349 Last updated 23 May 2026

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Devices
1
Registries
EUDAMED
FDA recalls
0

Catalogue1

  • Umg Ref 101001

    Class IIb EUDAMED Active

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.

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 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.

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

Information

Country
Germany
Address
41, Davidstraße, Goeppingen, Germany
Website
tzm.de/umg
Phone
+49 7161 5023-200
PRRC contact
Isabel Böhringer
EUDAMED SRN
DE-MF-000006349