It should be noted that the CE label on the product does not give the consumer a quality assurance. It only shows that the product is manufactured in accordance with the required safety conditions. CE label Thanks to these products, the products can easily be introduced to the European Union markets and cannot be rejected by these countries for legal reasons. In short, the CE mark is a sign that the product complies with the European Union New Approach Directives.
CE labeling is a must in all European Union countries. Besides, in our country, because of the Customs Union agreement, all products except agricultural products are obliged to bear the CE label.
In addition, in small European countries such as Monaco, Andorra, the Vatican and San Marino, although not legally necessary, the system is fully implemented due to close trade relations and geographical proximity.
However, CE criteria and standards have international validity and therefore CE marking is widely used by countries with intense commercial relations with Europe and frequently applied for CE standardization.
European Union New Approach DirectivesThe manufacturer, importer or distributor companies of the products which do not carry the CE label even though they are included in Turkey are subject to the sanctions shown in the relevant directives. On the other hand, in the export to the third countries from the European Union countries, the products do not have to carry the CE label.
Published by the European Union Electromagnetic Compatibility DirectiveThe Electromagnetic Compatibility Directive (89 / 336 / AT) issued by the Ministry of Industry and Trade on the basis of EMC (Electromagnetic Compatibility, EMC), is designed to eliminate or minimize the interference of electrical and electronic devices and systems. markings and their placing on the market.
Since such devices are considered low-risk products in the European Union Directives, companies producing these devices will first prepare a technical file. This technical dossier contains information and documents to demonstrate the characteristics of the respective products and their compliance with the essential requirements described in the directive. If the relevant directive foresees a conformity assessment process based on a quality system, the technical file is considered one of the quality system documents. The obligation to prepare a technical file begins as soon as the product is placed on the market.
The manufacturer then conformity assessment and puts the CE mark on the product if it believes that the product is in compliance with the directive.
The CE marking applies to the product, not to the manufacturer. Therefore, if the manufacturer produces more than one product, it has to carry out these operations separately for each product.
The TÜRCERT certification body primarily focuses on certification studies. However, in addition to these studies, it also offers technical services such as various test and inspection studies. Therefore, if there is a need to get more information about what the CE label means and how the electronic product CE certification works are carried out, do not hesitate to contact the experts and employees of the TÜRCERT certification body.