-To obtain a EU notified body CE authentication certificate, you can maximize the Gets the trust of consumers and market surveillance authorities;

-Can effectively prevent those irresponsible allegations appeared;

-In case of facing litigation, the EU notified body CE authentication certificate, the technical evidence will become legally binding;

-Once the punishment by EU countries, the accreditation body will work with business to take risks, thus reducing business risk.

ZKTEST is the world's leading certification testing and safety services, providing technical support to a wide range of industries and products and related services.

 

 

CE certification-sign

 

Free movement of goods is the cornerstone of the single market, the mechanism for achieving the free flow of goods is the CE mark, the mechanism built in to avoid creating new barriers to trade among the countries of the European Union, the mutual recognition and technical standards. The principles are as follows:-harmonization of legal documents (EC Directive) regulations is limited to the products of the basic requirements in order to facilitate the free flow of products within the European Union;

EU-harmonised standard includes the basic requirements of the directive;

-Application of EU harmonised standards and other standards is voluntary, can choose to apply the EU harmonised standards, can also apply other technical specifications to meet the essential requirements of the directive;

-Product meets the EU harmonised standards acknowledging, of course, to meet the essential requirements of the directive.

In order for the basic requirements set forth in the directive more workable, a series of EU harmonised standards developed by each Member State is responsible for the country's standards and harmonization. And harmonised standards are consistent with the spirit of the directive discussed also established the mechanisms and criteria for revision mechanism.

Because of provisions in the directive requires States to comply with the mandatory requirements, these requirements should be accepted as a minimum of preventive security risks or other hazards, different from the General technical requirements for trade in commercial and objective requirements for standardization.

In order to make the principles of the single market are implemented in practice, the EU further requirements of the product in accordance with the basic requirements of reliability assessment methods that people commonly known as CE certification:

-The introduction of modular concept of product evaluation, evaluation modules product evaluation process, in accordance with the evaluation procedures for the assessment of conformity of the product with CE mark;

-The introduction of a unified European Union harmonization of standards, quality management system standard (EN ISO 9,000 series) and assessment of quality assurance standards (EN45000);-at EU level, in the established assessment body accreditation system between Member States than between rating agencies and mechanisms;

-National mechanisms for establishing mutual recognition of product testing and certification areas;

-Simplify the between Member States, the field of quality systems between industry structure (such as measurement and calibration systems, testing laboratories, certification and inspection organization, recognized organization) differences;

-The use of mutual recognition agreements, cooperation and technical assistance projects, promote between countries other than Member States, and between Member States and the European Union in international trade. CE mark is designed to provide flexible products could actually work in practice conformity assessment route to meet the diversity of global economic integration under the trend of modern industrial production. Catering to all phases of product development, production, circulation (such as designing, proofing, production), product evaluation modules divided into technical documentation inspection, testing, quality assurance, as well as in practice by the producer or by a third party to complete the assessment.

Product prior to placing on the market and put into service must meet the essential requirements of all applicable EU directives and selects the appropriate product evaluation programs for product conformity assessment marks after CE sign. Marking CE marking the product is thought to have met all of the EU directive, Member States must take active measures to ensure the free flow of the single market, unless there is clear evidence that the product does not meet the basic requirements of applicable directives, or the product has not been a significant risk of an existing directive.

 

 

Product affixed CE symbol meaning

 

 

Significance of the CE mark is: affix the CE marking the product has passed the appropriate conformity assessment procedure and/or the manufacturer's Declaration of conformity, comply with the relevant EU directives, and as the product is allowed to enter the European Union market permits. The relevant instructions to affix the CE mark industrial products without CE mark, may not be listed for sale, affix the CE mark to market products, found that did not meet safety requirements, should be ordered to withdraw from the market, continuing violations of the directive relating to CE marking requirements will be restricted or prohibited from entering the EU market or forced to withdraw from the market. CE is not the mark of a quality mark, it is a representative of the product complies with the European safety/health/environment/health series mark of standards and directives. Sales in the European Union's mandatory CE mark on all products.