The European Directive on energy labeling (Regulations (EU) 2017/1369) establishing a framework that applies to energy-related products placed on the market or put into service. This provides for the labeling of such products and the provision of consistent information for energy efficiency, the consumption of energy and other resources by the products in use, and supplementary information thereon, to allow customers to choose more efficient products in order to reduce their energy consumption.
This Directive is part of the legislative framework for the free movement and marketing of products in the European community.
In general, the directive is intended to avoid the risks related to a product or to a phenomenon. The same product can be covered by several directives.
The purpose of this Directive is the defense of a common interest of European citizens and European companies.
The English name for this directive: Energy Labelling Regulation;
Its code is: (I) 2017/1369;
Previous directives on this subject, Today they are no longer in force: 2010/30/I, 92/75/CEE.
It is useful to know the references of the directives because they often are in the products or components documentation, but also in the European laws and regulations if they have not recently been updated.
Field of application: The Directive applies to energy-related products placed on the market or put into service. This directive does not apply to second-hand products, unless they are imported from a third country and the means of transport for persons or goods.
essential requirements: these products to be put on the European market must comply with essential requirements such as labeling of the products and the provision of consistent information for energy efficiency, the consumption of energy and other resources. Since 1 January 2019 registration is required for products in the European product data bank for energy labeling.
Main contents of the Directive
- Field of application
- essential requirements
- Obligations of the manufacturer
- Obligations of the other economic operators
- Free movement
- Presumption of conformity and harmonized standards
- Conformity assessment
- notified bodies
- CE Marking
These are the reasons that led to the writing of the Directive.
Field of application
The scope defines the categories of products or phenomena covered by Directive.
Often it is given a general criterion supported by explicit lists of products / phenomena that are subject to the Directive and product / phenomena that are excluded from the Directive in order to clarify the specific situations.
They also need to understand the scope of the Directive by providing the definition of key terms.
The essential requirements are requirements which the product must meet in order to be placed on the market.
Often the requirements are provided in Annex I to Directive.
Obligations of the manufacturer
The manufacturer (or his authorized representative in the European community) is the main person responsible for placing a product on the market. This chapter describes the requirements and procedures that it must follow, referring to the annexes to the directive to the extent of more detail.
Obligations of the other economic operators
Distributors and retailers are also responsible and liable if they trade items that do not comply with European directives. They must verify that the manufacturer did run the electrical safety testing, that the product is provided with the EC declaration of conformity and carry the CE mark.
Any importer must ensure that the procedures for the verification of conformity of the product have been performed, must check for the CE marking and ensure that the technical documentation of the product is available to national competent authorities.
Member States must presume that products bearing the CE marking comply with all the provisions of the applicable directives providing for the affixing. They can not therefore be prohibited, restrict or prevent the placing on the market and putting into service in their territory of products bearing the CE marking, unless the provisions relating to CE marking have not been applied improperly.
Presumption of conformity and harmonized standards
At the directives of our interest it is associated with a list of harmonized standards that is published in the European Official Journal.
The harmonized standards greatly facilitate the verification of compliance of a product with the requirements of Directive. In these standards is described in detail how the tests should be performed or other kinds of assessment needed to be assumed that a product complies.
If a product is available the harmonized standards covering all the requirements of Directive, if these rules are applied in a complete manner and the product passes all the tests provided in these rules, then it can be assumed that the product complies with the requirements of that Directive.
In the absence of harmonized standards adequate to the product path it is more complicated and expensive.
Equipping a suitable laboratory to perform the tests required by the Harmonized Standards thing is rather onerous. For this reason, manufacturers will often rely on external testing laboratories.
In Europe it is the body that can make an assessment of compliance by acting as a third party or whether the one made by the manufacturer and its trusted laboratories is correct.
In most cases, however, the use of a notified body is not provided or not required.
The products comply with all the provisions of the applicable directives providing for the CE marking must convey it. Such marking is, in particular, an indication that the products comply with the essential requirements of all applicable directives and that they were subjected to a conformity assessment procedure provided for by the Directives. Member States are also required to take the necessary measures to protect the CE marking.
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