Companies engaged in trade with and exporting to European Union countries must bear the CE mark if these products are covered by one or more of the EU Directives. Same time Avrupa Birliği In order for non-member countries to export to European Union countries, the products must bear CE marking.
CE certification represents the CE marking on the back of certain products sold in the European Economic Area (EEA) and in the European Union (EU). Literally, CE is the abbreviation of a French expression which means gelen European Conformity Kel. When a CE mark is placed on the back of a product, this mark indicates that the product can be distributed within the EU and EEA.
The CE marking consists of the initials of the French, the Conformité Européene and stands for European Eligibility. This practice is a legal requirement and the manufacturer must place CE marking on the products, the packaging and all documents providing information about the product.
CE markingis obliged to comply with a number of standards and requirements during production. This, on the other hand, allows consumers to know that this product is produced in accordance with the basic quality and safety standards.
For many people, the CE mark or mark indicates that the product is of good quality. However, the CE marking is not a quality certificate. Indeed, if the CE marked products are used for their intended purpose, it indicates that the product is safe and will not harm the safety of life and property for humans, animals and plants.
Made in 1996 between the European Union and our country customs union agreementestablishes free movement of goods other than agricultural products between countries of the Union. In this way, our country has gained a different position in relations with the European Union than other third countries. According to this, while the competition between the European Union countries is gained on the one hand, the standards determined by the union on the other hand have become compulsory for our country. In this way CE documenthas become an integral part of the production process. This will of course also increase the quality of the goods produced in our country. Because for the 23 product group, CE marking, which was required only for export to the European Union, was obligatory for the products to be put on the market after this date.
In other words, products that are included in the 23 product group, where CE marking is compulsory, cannot be sold to the European Union countries or to the country without CE marking.
What is CE Certificate
CE Certificate is a process that allows the CE marking to be attached to a product. Ideally, the product should begin at the development stage, because there are some well-known CE requirements during product safety, user health and environmental development. However, it is possible to issue CE certification for ready to use products. Products with CE certification must comply with European safety rules and only after being freely traded in the European Economic Area (EEA).
Six steps for CE Certificate
The CE certification scheme varies depending on the product category. The common schema contains the following steps:
- Find the EU Directive (s) applicable to your product
- Search for the necessary terms for your product
- Determine whether the product requires Assessment of a Notified Body
- Evaluate product suitability
- Creating and maintaining technical documentation
- Prepare the Declaration of Conformity and affix the CE Mark.
Products that require CE Certificate
The Certification Company assists with the preparation and approval of risk assessment or technical documentation at both the CE Certification and at any stage of the process. The product categories covered by our experts are as follows:
- Machinery and Installations (MD)
- Machines in potentially explosive atmospheres (ATEX)
- Electrical Equipment (LVD)
- Electronic devices: home and industry (EMC)
- Building Products (CPR)
- Medical Devices (MD)
- Personal Protective Equipment (PPE)
- Pressure Equipments (PED)
- Radio equipment
- Restriction on the Use of Certain Substances (RoHS)
- Other consumer products
CE Marking Systemhas a modular understanding that takes into account the characteristics of products and the risk ratios they carry with conformity assessment methods. In this system, at least one of the modules for determining the compliance with the relevant directives is mandatory in the design and production stages of the product. These modules cover various risk groups from A to H. Each module classifies the product according to the degree of danger. The testing and certification activities required for conformity assessment for low risk products are carried out by the manufacturer. In case of high risk products, these works are carried out by the notified bodies of the European Union.
If an accident occurs when using a CE marked product and one of the European Union claims that this product does not meet the required standards, the manufacturer must prove that it has taken the necessary measures to use the CE marking and that the accident is due to misuse. For this reason, it has to prepare the technical file in which the product information is put in full and without error and keep it for ten years.
The companies bearing the CE mark in their products benefit much from this. For example, the CE marked product has free circulation and marketing opportunities in the European Union countries. In accordance with the Customs Union agreement, industrialists must now place a CE mark on the product in order to sell their products in national and international markets. The CE marking indicates that the product conforms to the technical requirements of the European Union. In a sense it is like the passport of the product. However, the CE marking should not be regarded as a quality certificate or warranty certificate. In fact, CE is the initial level of product quality. Products below this level are considered unsafe and poor quality. If a product carries the CE marking, the European Union countries cannot reverse this product by providing legal justifications for norms.
As mentioned above, CE marking is not authorized for low-risk products. The manufacturer declares that the product is in compliance with the basic requirements and puts the CE marking on the product itself. In this respect, the responsibility is great. Therefore, they must carry this responsibility without disrupting the principle of trust.
A large number of cases are still pending before the European Union courts, where the conformity is declared and CE marked but not found to meet the basic requirements and which are collected from the market.
Since the CE marking is a sign attached to the products within the scope of many rules and directives which must be complied with in the European Union countries, the products which are covered by the said legislation and which will be placed on the market in the European Union member countries must bear this mark.
In order to make the free movement of goods within the framework of the European Union's technical legislation harmonization, the CE marking is in line with the new approach directives prepared in accordance with the new approach policy adopted by 1985 in order to make the legislation on technical and specific structures simpler and more general. all conformity assessment activities, these are the signs of primary health, safety and compliance of the consumer and the environment with the requirements of the Conformité Européenne.
The CE marking, which is the manufacturer's product safety guarantee statement and, in a sense, also referred to as the product's passport, is not a quality certification. CE mark; the product is located on;
It guarantees that it will not harm the environment with human, animal, plant health and safety and ensures that a single sign is used throughout the European Economic Area.
What does the CE Certificate of Conformity mean?
A CE certificate or certificate permits a product to move and sell freely in the European market. This sign proves that the product meets the environmental, safety and health requirements set by the EEA for the consumer. Compliance guarantee is not quality assurance. This means that the product meets the requirements to be sold in the EU.
It is important to be aware that the CE mark does not imply that a product is made in the EEA. A sign of European conformity means that the environmental, safety and health requirements identified by the EEA have been assessed and passed in order to sell a product in the EEA.
Products Sold in Europe and CE Mark;
CE brand standards are set according to EC Directives. An EU directive is a legal act of the European Union. The EU introduced regulations for many industrial products in 1985; These regulations include health, safety and environmental standards.
The set of standards and standards for standards are governed by two separate entities. While the European Union sets the standards for conformity to CE, the regulation of compliance does not have to go through the EU. Instead, adaptation can be implemented in a variety of ways.
Each distribution company has the ability to control the compliance of product manufacturers. If a distributor supplies its production customers, the manufacturer of the product must provide evidence for the CE marking.
Different European countries within the European Union have the ability to manage the application individually and locally.
Support can be obtained from third-party testing laboratories to assess whether CE certification standards are met.
The CE marking makes it easy for consumers to identify products classified by the Community as safe, and the products bearing this mark indicate compliance with the standards for packaging, labeling and safety to ensure that consumers are offered high quality products.