A product affixed with the CE mark conforms to essential health & safety requirements set out in European Directives. The CE mark is applicable to medical devices and is mandatory, which allows products affixed with it to be traded between the member states of the European Union and Norway, Iceland and Liechtenstein.
A product bearing the CE mark cannot be restricted, impeded or prohibited from being marketed in these countries. A product which does not comply with the provisions of the Directives, and therefore not CE marked, may not be placed on the market or put in to service in any of these countries.
A CE certificate is confirmation that the criteria necessary to acquire the CE mark have been met. The CE certificates for Neen Healthcare and its products can be found to your right under Related Documents.