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Yumen Bionics B.V.

Netherlands NL-MF-000018861 Last updated 17 Sep 2026

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Devices
1
Registries
EUDAMED
FDA recalls
0

Catalogue1

About

The Yumen EX-one is an arm supporter based on exoskeleton technology. It supports people with reduced muscle strength in the arms, so that daily activities become possible again.

Translated from the manufacturer's own website. Source

What Yumen Bionics B.V. makes

Yumen Bionics B.V. manufactures exoskeleton-based arm supports designed to assist individuals with reduced arm muscle strength. These devices aim to enable daily activities by providing external mechanical assistance to the upper limbs.

The company’s products fall under Class I medical devices and are registered in the EUDAMED database. The manufacturer is based in the Netherlands.

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 Yumen Bionics B.V. manufacture?

Yumen Bionics B.V. specializes in exoskeleton-based arm supports, such as the Yumen EX-one. These devices are designed to assist individuals with reduced muscle strength in their arms, helping them regain the ability to perform daily activities by providing external mechanical support to the upper limbs.

Where is Yumen Bionics B.V. based?

Yumen Bionics B.V. is based in the Netherlands. The company’s location in the Netherlands aligns with its focus on developing and manufacturing medical devices for the European market.

In which regulatory databases are Yumen Bionics B.V.’s devices listed?

Yumen Bionics B.V.’s devices are registered in the EUDAMED database, which is the European Union’s central registry for medical devices. This listing ensures transparency and compliance with EU regulatory requirements for Class I devices.

How are Yumen Bionics B.V.’s devices classified under EU regulations?

Yumen Bionics B.V.’s devices fall under Class I classification according to EU medical device regulations. This classification is typically assigned to low-risk devices, such as certain exoskeletons designed for arm support, where the risk to patient safety is minimal. Classification is determined based on factors like intended use, duration of use, and potential risks.

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

Information

Country
Netherlands
Address
69, Koninginnelaan, Veenendaal, Netherlands
PRRC contact
Micha Paalman
EUDAMED SRN
NL-MF-000018861