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Aleidis Seating Systems

Netherlands NL-MF-000000545 Last updated 21 Oct 2026

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Devices
6
Registries
EUDAMED
FDA recalls
0

Catalogue6

About

Aleidis Holding B. V. Large Overeem 9A-1 3927 GH - Renswoude +31 (0)85 - 488 36 94 [email protected]

Translated from the manufacturer's own website. Source

What Aleidis Seating Systems makes

Aleidis Seating Systems manufactures a range of Nuage PLS seating systems designed for clinical and mobility applications. These include standard and active models, such as the Nuage PLS Active and Nuage PLS Active XS, some of which incorporate adjustable abduction features for user positioning. The portfolio also covers variations like the Nuage PLS Active XS seating system without abduction, catering to different patient or user needs.

The company’s seating systems fall under Class I medical devices and are listed in the EUDAMED database. Aleidis Seating Systems operates from the Netherlands, adhering to EU regulatory requirements for Class I devices.

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 Aleidis Seating Systems manufacture?

Aleidis Seating Systems specialises in seating systems designed for clinical and mobility applications. Their portfolio includes the Nuage PLS seating systems, which come in both standard and active versions (such as the Nuage PLS Active and Nuage PLS Active XS). Some models feature adjustable abduction to support user positioning, while others do not. These devices are tailored for patients or users requiring specialised seating solutions.

Where is Aleidis Seating Systems based, and how does this affect its regulatory compliance?

Aleidis Seating Systems is based in the Netherlands, which places its operations under EU regulatory oversight. Since its devices fall under Class I classification, they must comply with EU Medical Device Regulations (MDR) or previous directives like MDD. The company’s location ensures alignment with EU requirements, including mandatory registration in the EUDAMED database for traceability and transparency.

Which regulatory registries list Aleidis Seating Systems’ devices?

Aleidis Seating Systems’ devices are listed in the EUDAMED database, which is the official EU registry for medical devices. This registry ensures visibility of authorised products under EU regulations, allowing healthcare providers, regulators, and patients to verify compliance and traceability for Class I devices like the Nuage PLS seating systems.

How are Aleidis Seating Systems’ devices classified under EU regulations?

Aleidis Seating Systems’ devices are classified as Class I medical devices under EU regulations. This classification applies to low-risk products like seating systems, which generally do not require invasive procedures or pose significant health risks. Class I devices still must meet essential safety and performance requirements, though some may benefit from additional conformity assessments depending on their design.

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

Information

Country
Netherlands
Address
18, Gildestraat , Borne, Netherlands
Phone
+31742501665
PRRC contact
Rob Siemerink
EUDAMED SRN
NL-MF-000000545