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CE Mark is a health and safety mark applied within the framework of the "New Approach" created by the European Union in 1985 in order to ensure the free movement of goods, and it is the abbreviation of the words 'Conformite European' and its meaning in the literature is 'European Conformity', Conformity with European Norms.

The CE Mark is a conformity mark with the New Approach Directives of the European Union, showing that the product on which it is attached is healthy and safe for humans, animals and the environment. It is not possible for a product within the scope of one or more of the 25 New Approach Directives to enter the EU market without carrying the CE Mark. For this reason, the CE mark can be defined as an "Industrial product passport" that allows the free movement of products in the European Union internal market.

The CE mark is a mark that allows the product to circulate freely within the EU, has to be used in the domestic market of Turkey as of January 1, 2004, is the manufacturer's warranty statement, but is in a way the passport of the product.

BENEFITS OF "CE" CERTIFICATE:

- CE Mark ensures the free movement and marketing of the product in EU countries,

- Industrialists are obliged to put the "CE" mark on the product in order to market their products at national and international level,

- CE Mark indicates the conformity of the product with EU technical legislation,

- CE Mark functions as a kind of product passport,

- The CE Mark is definitely not a quality mark and a guarantee document,

- CE Mark shows the level where the quality starts,

- CE Mark, products below this level are classified as unsafe and are not placed on the market, therefore they are considered to be of poor quality,

- It is not possible to return the CE marked product in EU countries, by presenting legal justifications related to the norms,

- The CE Mark is an indication of compliance with the New approach directives.

- All new products manufactured in member countries or third countries,

- Used or second-hand products imported from third countries,

- Significantly modified products, which are subject to the provisions of the directives as if they were new products,

It must bear the CE mark.

- The Directive or Directives Within the Scope of the Product, Which Requires CE Certificate, Are Determined.

- After the Directive or Directives are Determined, the Standard or Standards of the Product within the Scope of the Directive or Directives are Determined.

- The Road Map is Examined within the Scope of the Directive or Directives and the Most Appropriate Road Map is Selected.

- The Most Appropriate Module (Conformity Assessment Method Envisaged to Determine Conformity with Basic Requirements) is Selected within the Scope of the Directive or Directives. (8 Basic Modules and 8 Variants Of These Can Be Combined With Each Other In Various Ways To Create A Whole Conformity Assessment Procedure. As a General Rule, a Product Is Subjected to Conformity Assessment According to a Module During the Design and Production Stages).

- It is determined whether the product is a Risky Group Product or not. If it is a Risky Group Product, the Most Appropriate Certification Offer is received from Notified Body.

- It is checked whether the product is produced in accordance with the standards.

- Risk analyzes in the mechanical, electrical and construction structure of the product are made. As a result of the risk analysis, there may be some minor changes that may occur on the product related to safety. After the meetings with our experts and the technical staff of the company, the final state of the product is determined.

- If the Product Needs to be Tested within the Scope of Standards or Standards, the Most Appropriate Offer is Obtained for Testing from an Accredited Testing Organization (Domestic or International).

- Required Trainings on the Standard or Standards to be Applied in the Manufacturing Phase are given to the Technical Personnel of the Company by Experts.

- Work Orders are prepared to ensure that the production to be applied in production conforms to the standards, and if there is a Quality Management System applied in the company, these work orders are added to the Quality Management System Procedures and Implemented in the Most Efficient Way.

- Product Installation, Commissioning, End User and Maintenance Manuals are created within the scope of Directives and Standards.

- Labeling and marking of the product is done in accordance with the Directives and Standards.

- The Technical File of the Product is Prepared. The Technical File is the file containing all the technical information and reports related to the product, which must be kept in the manufacturer for 10 years.

- The CE Declaration of the product is prepared.

- CE Mark is attached to the product.

If a situation that does not comply with the regulations is detected, the manufacturer of the product or its authorized representative established in Turkey is obliged to ensure that the product complies with the provisions regarding the CE conformity mark and to end this violation. In case the non-compliance continues, the Ministry shall take all measures regarding the restriction or prohibition of the supply of the product to the market or its withdrawal from the market, within the framework of the authorities given to it by law.