Electric wheelchair manufacturers are reminded that their products must be safe, robust and conform to the requirements in Annex I of the European Medical Device Directive 93/42/EEC before they can be offered onto the market in the European Union (EU). This requires adequate testing against the correct standards.
Under the European Medical Directive, wheelchairs are classified as Class I. This means the manufacturer is responsible for declaring the product complies with the directive. Furthermore, because it is supplied in non-sterile condition and does not have a measuring function, the manufacturer does not need to consult an independent Notified Body.
Under the terms of the European Medical Directive, manufacturers must compile a technical dossier containing, inter alia, a risk analysis and their own Declaration of Conformity (DoC) that the product conforms to applicable standards. Following this, the manufacturer can place the CE mark on their product to show compliance.
Wheelchairs and scooters are classified according to their intended use:
To learn more about these classes, view the SGS article: “Accessing the EU Marketplace with Safe and Compliant Electric Wheelchairs”.
Applicable standards for wheelchairs and scooters are:
First published in 1999, EN 12184 is now on its fourth iteration – EN 12184:2014. It covers:
· Electrically powered wheelchairs
It applies to products where the maximum speed does not exceed 15km/h and that are intended to carry only one person with a mass no greater than 300kg.
The standard covers several aspects of wheelchair design, including:
The standard largely relies on normative reference documents, especially for test methods. In especial, it references the ISO 7176 series, either whole or in part. Therefore, evaluation against these will confirm adherence to EN 12184.
The ISO 7176 documents referenced in EN 12184 are:
To gain access to markets in the EU, manufacturers of electrical wheelchairs must ensure they conform to the requirements of the European Medical Directive. While it is not mandated that they must consult an independent Notified Body, they must perform correct and adequate testing to ensure products are safe, robust, and adhere to applicable regulations.
SGS Electrical and Electronic Testing Services
We offer a comprehensive range of services to help manufacturers of electric wheelchairs access the European market. Our experts are fully conversant with the requirements for the European Medical Device Directive and offer consultancy and testing solutions to help expediate your access to the market. Learn more about SGS Electrical and Electronic Testing Services.
For more information, please contact:
AJ Yang 楊正吉
Senior Engineer
Email: crs.media@sgs.com
Website: www.sgs.com/ee
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