access synopsis of the Article to the market in the sense that the authorities are not allowed to require all kinds of requirements to be fulfilled. SMC product applicable EU directives have been revised based on the adoption of the European Union's New Legislative Framework (NLF) Decision 768/2008/EC. By applying the relevant harmonised European standards, you will be able to fulfil the essential legislative requirements of the directives. You can view the EC New Approach Directives guidance from the Europa website. CE marking does not mean that a product was made in the EEA, but states that the product is assessed before being placed on the market. It is the manufacturers responsibility to draw up and sign an EC DoC proving that the product meets the requirements. This is not obligatory for all products, so it is important to check whether the involvement of a Notified Body is required. They will take appropriate action in the event of improper use of the marking and provide for penalties for infringements, which may include criminal sanctions for serious infringements.
You may also be liable for a fine and imprisonment. Identify the directive(s) and harmonised standards applicable to the product There are more than 20 directives setting out the product categories requiring CE marking. If you are looking for the Declarations of Conformity applicable to products with manufacturing batch codes UQ backwards (before April 2016 please click here, search, series, description, documents 50-VFE, solenoid Valve. Not only can they investigate, but they can also take measures against infringements. You must be able to present the technical documentation and EC DoC to the relevant national authorities, if requested. Keep documentation for CE marking Please refer to the specific directives and/or regulations, and also our guidance documents. You must keep certain documentation once you have placed the CE marking onto your product.