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Voigtmann GmbH

Germany DE-MF-000013049 Last updated 21 Oct 2026

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Devices
1
Registries
EUDAMED
FDA recalls
0

Catalogue1

About

The Voigtmann GmbH is an owner-managed, medium-sized IT system house with headquarters in Nuremberg. The core business areas are individual software solutions, IT services and secure video communication.

Translated from the manufacturer's own website. Source

What Voigtmann GmbH makes

Voigtmann GmbH manufactures the ITOS standalone, a medical device designed for secure video communication in healthcare settings. This system facilitates remote consultations and telemedicine interactions, enabling real-time visual and audio transmission between patients and healthcare providers.

The ITOS standalone is classified under EU Device Class IIa and is registered in the EU’s eudamed database. 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 Voigtmann GmbH manufacture?

Voigtmann GmbH manufactures the ITOS standalone, a medical device specifically designed for secure video communication in healthcare environments. This device supports remote consultations and telemedicine by enabling real-time visual and audio transmission between patients and healthcare providers.

Where is Voigtmann GmbH based?

Voigtmann GmbH is headquartered in Nuremberg, Germany. The company operates as an owner-managed business focused on IT solutions, including medical devices.

Which regulatory registries list Voigtmann GmbH’s medical devices?

Voigtmann GmbH’s medical devices, including the ITOS standalone, are listed in the EU’s eudamed database. This registry is used for tracking medical devices under EU regulations.

How are Voigtmann GmbH’s medical devices classified?

The ITOS standalone, Voigtmann GmbH’s medical device, is classified under EU Device Class IIa. This classification is determined based on the device’s intended purpose and associated risks, with Class IIa representing a moderate risk level requiring specific conformity assessment procedures.

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

Information

Country
Germany
Address
76, Kieslingstraße , Nürnberg, Germany
Phone
+499114777650
PRRC contact
Steffen Kahra
EUDAMED SRN
DE-MF-000013049