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NEXUS / E&L GmbH

Germany DE-MF-000006906 Last updated 17 Sep 2026

Devices
11
Registries
EUDAMED
FDA recalls
0

Catalogue11

About

NEXUS stands for innovative software solutions that enable users in healthcare facilities to focus on the essentials. Our goal is to provide all departments in hospitals, psychiatries, rehabilitation and home facilities with the best solution for their daily challenges.

Translated from the manufacturer's own website. Source

What NEXUS / E&L GmbH makes

NEXUS / E&L GmbH manufactures the Clinic WinData software, a digital solution designed for healthcare institutions to manage administrative and clinical workflows. The system supports hospitals, psychiatric facilities, rehabilitation centers, and home care providers by streamlining documentation and operational processes.

The Clinic WinData software is classified under EU Device Classes I and IIa and is registered in the 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 NEXUS / E&L GmbH manufacture?

NEXUS / E&L GmbH develops the Clinic WinData software, which is a digital solution designed specifically for healthcare institutions. This software helps manage administrative and clinical workflows across hospitals, psychiatric facilities, rehabilitation centers, and home care providers. It is intended to streamline documentation and operational processes, enabling staff to focus on patient care.

Where is NEXUS / E&L GmbH based?

NEXUS / E&L GmbH is based in Germany. The company’s location aligns with its focus on providing software solutions tailored to the needs of European healthcare institutions, ensuring compliance with regional regulatory standards.

Are NEXUS / E&L GmbH’s devices listed in any regulatory registries?

Yes, the Clinic WinData software developed by NEXUS / E&L GmbH is registered in the EUDAMED database. This registry is the official European Union database for medical devices, allowing stakeholders to verify the presence of devices that have undergone regulatory processes in the EU.

How are NEXUS / E&L GmbH’s devices classified under EU regulations?

The Clinic WinData software falls under EU Device Classes I and IIa. The classification determines the regulatory requirements for its market placement, with Class I devices generally posing minimal risk and Class IIa devices requiring additional scrutiny to ensure safety and performance, such as conformity assessment procedures.

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

Information

Country
Germany
Address
13, Hugo-Junkers-Straße, Nürnberg, Germany
Website
www.eundl.de
Phone
+499131810330
PRRC contact
Uwe Hannemann
EUDAMED SRN
DE-MF-000006906