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Neuroventis

Belgium BE-MF-000032626 Last updated 21 Oct 2026

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Devices
5
Registries
EUDAMEDGUDID
FDA recalls
0

Catalogue5

About

Neuroventis emboldening people with neurological disorders. Learn how our technology is changing the world of neurological care.

From the manufacturer's own website. Source

What Neuroventis makes

Neuroventis makes software applications and dashboards for managing neurological conditions, including epilepsy and migraines. Their products include the Helpilepsy Dashboard and Application, as well as the MigraineManager Dashboard and Application. These are digital tools designed to support people with neurological disorders.

The company's portfolio is classified as Class I devices and is listed in the Eudamed registry. Neuroventis is based in Belgium. The devices are subject to regulatory oversight, with individual products authorized for use.

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 Neuroventis develop?

Neuroventis develops software-based medical devices, specifically digital applications and dashboards that help manage neurological conditions such as epilepsy and migraines. This conclusion follows from the listed examples—Helpilepsy and MigraineManager dashboards and applications—which are described as tools for supporting people with these disorders.

Where is Neuroventis headquartered and which regulatory registry lists its devices?

Neuroventis is based in Belgium, as indicated by the country code BE in the data. Its devices are listed in the European Union's Eudamed registry, which is explicitly mentioned as the registry where the company's Class I devices are recorded.

How are Neuroventis' devices classified under EU medical device regulations?

All of Neuroventis' products are classified as Class I devices. This classification is directly stated in the device data, meaning they are considered low-risk medical devices and are subject to the corresponding regulatory requirements for that class.

Are Neuroventis' individual products approved or cleared for use?

The data notes that each product is individually authorized for use, which means that while the company itself is not approved, each specific software application or dashboard has undergone the necessary regulatory assessment to be permitted for clinical or consumer use.

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

Information

Country
Belgium
Address
35A, Groeneweg, Overijse, Belgium
PRRC contact
Ruth Beckers
EUDAMED SRN
BE-MF-000032626
DUNS number
371379519