Safe non-food consumer Products in the EU and China
The essential objective of a conformity assessment procedure is to demonstrate that products conform to the requirements expressed in the provisions of all relevant legislation. There are many hazards which can occur in poorly designed and manufactured electrical appliances. Fortunately, there are harmonised standards which can assist in the design process.
The manufacturer must, however, think about more than just the design process. They must consider the product’s normal period of use i.e. throughout its lifetime. Consideration should also be given to who will be using the electrical appliance and how it might be accidentally misused.
A conformity assessment procedure is required for every single electrical appliance for the EU market. Manufacturers have this obligation whether they make complex or basic electrical appliances. The assessment of the conformity of an appliance must be done before it is placed on the market.
To comply with legal requirements, manufacturers have to follow six necessary steps in order to make their products ready for the market:
1) Identify the directive(s) and harmonised standards applicable to the product.
The essential requirements products have to fulfil (e.g. safety) are harmonised at EU level and are set out in general terms in the Directives. For electrical household products connected to AC mains, the key piece of legislation is the Low Voltage Directive.
It is quite likely that other legal requirements will also apply including for instance the Electromagnetic Compatibility directive, the ROHS directive and in some cases also the Ecodesign directive and the energy labelling directives with its implementing regulations. This will depend upon the type of product.
A manufacturer must demonstrate that all applicable legal requirements are met. Harmonised European standards are issued with reference to the applied directives and express in detailed technical terms the essential requirements.
2) Verify the product-specific requirements.
It is up to manufacturer to ensure that their product complies with the essential requirements of the relevant EU legislation. Full compliance of a product to the harmonised standards gives to the product the ‘presumption of conformity’ with the relevant essential requirements.
It is important for manufacturers to understand the relevant standards.
Harmonised standards exist in the EU for electrical appliances. An electrical appliance complying with these standards is presumed to be in conformity with the essential safety requirements set out in the Low Voltage Directive if the standards are referenced in the Official Journal of the European Union (OJEU). Further information on, and the list of harmonised standards for electrical appliances is available from here.
3) Identify whether an independent conformity assessment is required from a Notified body.
Each directive covering a particular product specifies whether an authorised third party (Notified Body) must be involved in the conformity assessment procedure necessary for CE marking.
Further information can be found in the ‘Conformity assessment’ module.
4) Test the product and check its conformity to the EU legislation.
Risk assessment plays an important part in the procedure. By applying the relevant harmonised European standards, the manufacturer will be able to fulfil the essential legislative requirements of the directives.
5) Draw up and keep available the required technical documentation.
The manufacturer has to establish the technical documentation required by the Directive(s) for the assessment of the product’s conformity to the relevant requirements and a risk assessment. Together with the EC declaration of conformity, the technical documentation must be presented on request to the competent national authorities.
6) Affix the CE mark to your product and EC Declaration of Conformity.
The CE Marking must be affixed by the manufacturer, according to its legal format visibly, legibly and indelibly to the product or its data plate. If a Notified Body was involved in the production control phase, its identification number must also be displayed. The essentials of the CE mark are:
Further information can be found in the ‘CE marking’ module.
Learn more about conformity assessments and how they work in practice
Learn more about CE marking
Regulation 765/2008 contains details about the CE mark in Annex II and its use.
This is an example of the CE mark and it is available in different formats to download from the European Commission website.
Testing is one of the activities in the conformity assessment process. Accreditation is an internationally recognised way of ensuring that laboratories and certification bodies are qualified to do their job. Laboratories are accredited by national accreditation bodies.
If a manufacturer wants to search for accredited bodies, there are a number of websites that can be checked:
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