1. What is CE certification?
CE certification is the "main requirement" that constitutes the core of the European Directive. In the Resolution of the European Community on May 7, 1985 (85/C136/01) on the New Methods of Technical Coordination and Standards, the "main requirement" that needs to be used as the purpose of developing and implementing the Directive has a specific meaning, that is, it is limited to basic safety requirements that do not endanger the safety of human, animal, and goods, rather than general quality requirements. The Harmonized Directive only specifies the main requirements, and general directive requirements are the task of the standard.
2.What is the meaning of the letter CE?
In the EU market, the "CE" mark is a mandatory certification mark. Whether it is a product produced by internal enterprises in the EU or products produced in other countries, in order to circulate freely in the EU market, it is necessary to attach the "CE" mark to indicate that the product meets the basic requirements of the EU's "New Methods for Technical Coordination and Standardization" directive. This is a mandatory requirement of EU law for products.
3.What is the meaning of the CE mark?
The significance of the CE mark is to use the CE abbreviation as a symbol to indicate that the product with the CE mark complies with the essential requirements of the relevant European directives, and to confirm that the product has passed the corresponding conformity assessment procedures and the manufacturer's declaration of conformity, truly becoming a passport for the product to be allowed to enter the European Community market for sale.
Industrial products required by the directive to be marked with the CE mark shall not be put on the market without the CE mark. Products that have already been marked with the CE mark and enter the market shall be ordered to be withdrawn from the market if they do not meet safety requirements. If they continue to violate the provisions of the directive regarding the CE mark, they shall be restricted or prohibited from entering the EU market or be forced to withdraw from the market.
The CE mark is not a quality mark, but a mark that represents that the product has met European standards and directives for safety, health, environmental protection, and hygiene All products sold in the European Union must be mandatory with the CE mark
4.What is the scope of application of CE certification?
Both the European Union (EU) and the EEA countries in the European Economic Area (EEA) need the CE mark. As of January 2013, the EU has 27 member countries, three member countries of the European Free Trade Association (EFTA) and Türkiye, a semi EU country.
CE testing
Post time: May-21-2024
