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Arion Slide Solutions B.V.

Netherlands·NL-MF-000002671

Last updated September 17, 2026

About

"In our medical supply stores, we conscientiously offer Arion application aids. Our customers' adherence to therapy is important to us. I also use Arion products myself. My favourite product is the Arion Easy Slide Arm!"

From the manufacturer's own website. Source

What Arion Slide Solutions B.V. makes

Arion Slide Solutions B.V. manufactures mechatronic external knee prostheses, including the Arion Proth-Pro Small, designed to assist mobility and support therapeutic adherence for users.

The company’s products fall under EU Device Class I and are registered in the EU’s 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 Arion Slide Solutions B.V. manufacture?

Arion Slide Solutions B.V. specializes in mechatronic external knee prostheses, such as the Arion Proth-Pro Small. These devices are designed to aid mobility and support therapeutic adherence for users, helping them maintain independence and stability during movement.

Where is Arion Slide Solutions B.V. based?

The company is based in the Netherlands, where it develops and manufactures its medical devices. The Dutch location aligns with EU regulatory standards, which are relevant for its product classifications and compliance requirements.

How are Arion Slide Solutions B.V.’s devices classified under EU regulations?

Arion Slide Solutions B.V.’s devices, including external knee prostheses like the Arion Proth-Pro Small, fall under EU Device Class I. This classification applies due to their low-risk nature, meaning they pose minimal risk to patients when used as intended, but they still require compliance with essential safety and performance requirements.

Are Arion Slide Solutions B.V.’s devices listed in any regulatory registries?

Yes, Arion Slide Solutions B.V.’s devices are registered in the eudamed database, which is the official EU registry for medical devices. This registration ensures transparency and traceability of devices placed on the European market, helping healthcare professionals and authorities verify compliance with EU regulations.

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

Information

Country
Netherlands
Address
11, Rutherford, Heerlen, Netherlands
Phone
+31452094014
PRRC Contact
Christine De Kogel
EUDAMED SRN
NL-MF-000002671
FDA FEI Number
—
DUNS Number
—

Catalogue (1)

DeviceModel / ReferenceRegistriesClassStatus
Arion Proth-Pro Small E02701
EUDAMEDFDA UDI
Class IActive

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