CE certificate is a type of document obtained for products to be sold in European Union countries. CE marking is mandatory on products. Products covered by the CE certificate; They can be called cosmetics, food, textile and electronic products. In addition, CE certification is required in categories such as medical devices and electrical devices used in industry. Products included in the CE regulation must be filed in accordance with the regulation. Following the necessary tests, technical file and calculations, products deemed suitable are entitled to receive CE certification.
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Some product categories have been retained for this document. Among these products; Low voltage devices, machines, pressure vessels, hot and cold water boilers, gas burning devices and toys are included. Afterwards, products such as materials used in construction, elevators, freezers, boats, manual scales are products suitable for CE certification. Products to be sold in the European Union market are evaluated in two risk groups: low and high. If the risk of the product is high, it must be approved through organizations determined by third parties.
CE certificate is issued after the correct preparation of the technical file created for the products and the approval of the tests to be carried out. If the product does not meet the required qualifications, no documentation can be requested for the product. These conditions are generally kept valid for risky product groups. Organizational approval is not required for products with low risk. You can get help from our company, which provides consultancy, for all your questions about CE certificate and CE marking. We carry out all the necessary procedures flawlessly and share with you all the steps that need to be followed for the document.
What is the CE Certificate Regulation?
We can say that the CE certificate regulation is a set of rules for issuing CE certificates to products that will be sold in EU member countries. In other words, it is a set of regulations that determine whether products are entitled to the CE mark after the conformity assessment is completed. Thanks to this regulation, many products are produced and sold in European Union countries. CE certificate is obtained to certify that a product complies with EU regulations. Products with completed CE marking are products that have been deemed suitable for the European market and do not pose any obstacle to sale.
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In order to receive the certificate, the product must be evaluated and technical file preparations must be completed. Certified products are kept in compliance with EU regulation. The main reason for preparing regulations for products is to ensure that the materials used are harmless. The first rule in the regulation is that the materials used do not harm people, the environment and animals. Another feature that will be required for the product is that it is safe.
Within the scope of European Union regulations, products are required to have a CE certificate and bear the CE mark. If the product cannot fulfill any of the regulations, it is prohibited to bear the CE marking. In fact, in some cases, more than one regulation may apply to a product.
The CE mark on equipment, machinery or medical devices indicates the suitability of the product in terms of health and safety. In other words, the CE marking on the product does not give definitive information about the product quality. However, it should be known that every product bearing the CE mark has been subjected to certain tests and has been produced in a way that does not harm the environment. In addition, the necessary technical file and test report have been prepared for the suitability of the product.
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