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CE "mark is a safety certification mark, the manufacturer is considered open and enter the European market passport CE behalf of the European the unified (CONFORMITE EUROPEENNE) who posted" CE "mark products can be sold in EU member states, not required to comply with the requirements of each member, in order to achieve a free flow of goods in the EU member states within.
Background
CE certification mode - mode CE certification -
Following do detailed explanation
Factory self-control and certification Module A
Second, by the testing agency to review Module B
CE certification - applicable range:
CE certification mode
CE certification - Equipment
CE certification - inconsistent consequences
The main cause of the the CE certification costs CE certification costs
CE certification fees may apply for pioneering grant funds:
Understanding of the cost of a CE certification, select the CE certification bodies
, CE certification time
CE certification costs with product instructions
IV, EMC and LVD specific meaning
LVD Low Voltage Directive 73/23/EEC
EMC EMC Directive 89/336/EEC
Machinery CE certification costs
CE certification time
CE certification scope and instruction
CE certification and the EU Directive What is the RoHS Directive
ROHS implementation of significance
The difference between GS and CE
CE certification test project electromagnetic compatibility test items (EMC)
Safety test item (LVD)
Who is the object of the acceptance of the CE mark certification? CE certification - instructions
CE certification - concept
CE certification - the origin of
CE certification - mode
CE certification - meaning, the need to apply for CE certification
Apply for the benefits of CE certification
CE certification - flag
CE certification - logo size requirements
Who is the CE mark certification accepted object
CE certification - Process
CE certification - program
1. Confirm the exporting country
2. Confirm the product category and the relevant EU directive
3 Specify the European Union (EU authorized agent authorized representative)
4. Confirm the certification desired mode (Module)
5 self-declaration mode or through third party certification institutions
6. Creating technical documentation, maintenance and update of medical devices certified background CE certification - mode
CE certification - can be explained in detail mode following
Factory self-control and certification Module A
Second, by the testing agency the Assessment Module BCE Certification - applicable range: the CE authentication mode CE certification - Device CE certification - inconsistent consequences CE certification costs
Understanding of the primary cause of the costs of CE certification CE certification costs may apply pioneering grant funds: CE certification costs
First, select the CE certification bodies, CE certification time, CE certification costs Products Directive IV, EMC and LVD specific meaning LVD Low Voltage Directive 73/23/EEC EMC EMC Directive 89/336/EEC five mechanical CE certification costs range of CE certification of CE certification time and some instructions CE certification EU Directive
What is the RoHS Directive ROHS implementation of the significance of the distinction of the GS and CE CE certification test project
Who is the object of the acceptance of the electromagnetic compatibility testing project (EMC) Safety Test Project (LVD) CE certification mark? CE certification - instructions
Name Directive No. Effective Date
Simple pressure vessels 87/404/EEC 1992 July 1, 2011
Toy 2009/48/EC 2011 July 20, 2011
Building supplies 89/106/EEC 1991 June 27, 2011
EMC 2004/108/EC 2004 December 15, 2010
Machinery 2006/42/EC 2009, December 29, 2011
Personal Protective Equipment 89/686/EEC 1995 July 1, 2011
Non-automatic weighing instruments 90/384/EEC 1993 January 1, 2011
Initiative implantable medical devices 90/385/EEC 1994 December 31, 2011
Gas appliances 90/396/EEC 1995 December 31, 2011
Boilers 92/42/EEC 1998 January 1, 2011
Blasting 93/15/EEC 2003 January 1, 2011
Generic Medical Devices 93/42/EEC 1998 June 15, 2010
Low-voltage electrical safety 2006/95/EC 2006 December 12, 2011
Blasting environment used equipment 94/9/EC 2003 June 30, 2010
Water sports vessels 94/25/EC 1998 June 16, 2010
Lifting equipment 95/16/EC 1999 July 1, 2010
Household refrigerating appliances 96/57/EC 1999 September 3, 2011
Pressure Equipment 97/23/EC 2002 May 29, 2011
Communications equipment 98/13/EEC 1992 11 Day / May 1, 1995
In vitro diagnostic medical devices 98/79/EC 2003 December 7, 2010
Radio and telecommunications terminal equipment 99/5/EC 2000 April 8, 2011
Cableway 2000/9/EC 2002 May 3, 2011
Environmental noise equipment 2000/14/EC 2002 on January 30, 2010
Fluorescent lamp ballasts 2000/55/EC 2000, October 8, 2011
CE certification - concept
"CE" mark is a safety certification mark, the manufacturer is considered to play
Open passport to enter the European market. CE on behalf of the the European unified mobile the picture (CONFORMITE EUROPEENNE). A mandatory certification mark "CE" mark in the EU market, the EU internal production of products or the products of other countries, in order to circulate freely in the EU market, must affix the "CE" mark, to indicate that the product comply with the basic requirements of EU "technical coordination and standardization of new methods" instruction. This is a mandatory requirement of EU law on the products. Must be headquartered in the EU member states, certification bodies can issue certificates. Since the late 1980s, a group of foreign certification agencies stationed in China.
CE certification - the origin of
CE is an abbreviation of the French, in English means "European Conformity European Community, many countries, in fact, CE or EC language
Species "EC" an abbreviation of the phrase, the original phrase in English the EUROPEAN COMMUNITY abbreviations EC, after the EC in French is COMMUNATE EUROPEIA, the Italian COMUNITA Europea, the Portuguese COMUNIDADE EUROPEIA Spanish for COMUNIDADE EUROPE, so change the EC for the CE. Of course, also wish the CE as a
CONFORMITY WITH EUROPEAN (DEMA ND) (in line with European (requirements)), constitute the the European Directive core requirements "in the technical coordination and standards of the EC, May 7, 1985 (85/C136/01) No." a new resolution on the need for the development and implementation of the directive purpose "requirements" has a specific meaning, that is limited to the basic safety requirements of the products do not endanger the security of humans, animals and goods, rather than the general quality requirements, coordination of instruction Only the provisions of the main requirements of the general instructions to the standard task. The product complies with the relevant instructions about major requirements, will be able to attach a CE mark, rather than ruled that the provisions of the general quality of the ability to use the CE mark in accordance with the relevant standards. Therefore, the exact meaning: CE mark is a safety inspection mark rather than quality mark. In the 1940s, Western European countries feel that, in the United States and the Soviet Union between the two powers to ensure their own safety, improve its international status, speed up economic development, must unite, thus pushing the process of European integration. European integration can be divided into five levels: the establishment of a free trade zone, customs union, unified market, economic and monetary union and political union.
CE certification - mode
CE certification can be said is the world's most advanced product conformity assessment mode, it is the first to introduce the concept of modules, the assessment of the application of the CE mark by the Evaluation Module and assessment procedures by these assessments. In general, the assessment module are the following:
A: self-proclaimed (self-proclaimed by the producers, and provide the product key technical information) CE certification mark
B: type tests (carried out by the European Notified Body products fully tested)
C: Notified Body for the production of factory inspection
D: Notified Body for factory production and its quality management system review
E: Notified Body for review of quality management system for traders and other middlemen
F: Notified Body for bulk products imported into the EU ashore review
G: Notified Body for type testing of the product has not been imported into the EU, including the comprehensive review of the type test
The different instructions composition assessment procedures by which modules should be done. : Low Voltage Directive (LVD), Electromagnetic Compatibility Directive (EMC) consisting of A; Gas Appliance Directive (GAD) by BC, BD, BE or BF. The following can be explained in detail: a factory self-control and the Certification Module A (internal production control) 1 for a simple, high-volume, non-hazardous products, applies only to manufacturers who wish to apply European standards. Factory self-qualified assessment, self-declaration. 3, the technical documentation submitted by national institutions save decades, based on the available assessment and inspection to determine whether the product complies with Directive, producers and even to provide product design, production and assembly process for inspection. 4, do not need to declare their production process to ensure that products meet the requirements. Module Ab
1, factory production is not made in conformity with the European standards.
2, test institutions of special parts for random testing.
Second, by the testing agency to review Module B (EC type-reviewed)
The factory sent a sample to test it select agencies for review and technical documents, a certificate issued by the testing agency.
NOTE: The only B is insufficient to constitute the use of the CE. Module C (with the type [sample] line) + B
Factory for Conformance Statement (by type of certification), the statement ten years. Module D (produced CE certification agencies
Process Quality Control) + B:
The mode concerned about the control of the production process and the final product, the factory in accordance with a method approved by the testing agency (quality system, EN29003) production and its products with the certification statement based on the same type (Declaration of Conformity). Module E (product quality control) + B
This mode is only concerned about the control of the final product (EN29003), the same Module D. Module F (product testing) + B
The plant is to ensure that the production process to ensure that products meet the requirements for a Declaration of Conformity. Recognized testing organization full inspection or random checks to verify the compliance of their products. Testing authority certificate. ModuleG (individually tested) factory Statement complies with Directive requirements, and testing agencies submit product technical parameters, and examine individual product testing agency awarded a certificate. Module H (comprehensive quality control) mode is concerned about the design, the control of the production process and the final product (EN29001). The rest with Module D + Module E. Which mode F + B, mode G applies to a particularly high degree of risk.
CE certification - meaning
A need to apply for CE certification
CE certification for national products in the European market trade provides a unified technical specification to simplify trade procedures. Product of any country to enter the EU, the European Free Trade Area of the need for CE certification, to affix the CE mark on the product. CE certification is the product passes to enter the markets of the EU and EFTA countries. CE certification means that the product has reached the safety requirements of the EU directives; business-to-consumer and a commitment to increase consumer trust; affixed with a CE mark the product will reduce the risk of sales in the European market. These risks include the following:
Risk of detention and investigation of customs;
● investigated the risk of market oversight bodies;
● peers for competitive purposes allegations risk.
Apply for the benefits of CE certification
● EU laws, regulations and harmonization of standards is not only the quantity, but the content is very complex, so to obtain the designated agency of the European Union to help is a time-saving, labor-saving, but also reduce the risk wise;
● obtained by the designated agency of the European Union's CE certification, you can maximize access to the trust of consumers and market oversight bodies;
● be effective in preventing the emergence of those irresponsible allegations;
● In the case of the face of litigation, the designated agency of the European Union CE certification, will be the technical evidence has the force of law;
● once punished by the EU countries, the certification body with enterprise risk, thus reducing the risk of the enterprise.
CE certification - flag
CE certification
Intertek CE style
The free movement of goods is a cornerstone of the single market, to achieve the free movement of goods mechanism is the CE mark, the establishment of the mechanism to avoid new trade barriers between EU countries, on top of mutual recognition and coordination of technical standards. The principles are as follows: - the harmonization of the legal documents (EU Directive) under the product is limited to the basic requirements for free circulation within the EU in order to facilitate the product;
- EU harmonized standard contains the basic requirements of the Directive;
- EU harmonized standards and other standards applicable voluntary products can select the applicable EU harmonized standards, can also be applied to other technical specifications to meet the basic requirements of the Directive stipulates that;
- The products meet the EU harmonized standards course recognized as meet the basic requirements of the Directive.
Basic requirements for more operational, a series of EU harmonized standards drawn up by the Member States, is responsible for the country's standard with which coordinated in order to make the products specified in the instruction. And whether the harmonized standards discuss the mechanism and standard mechanism for amending the directive spirit also will be established.
Due to the requirements specified in the instruction countries must comply with the mandatory requirements, these requirements should be recognized minimum program to prevent safety hazards or other hazards, the technical requirements of the commercial is different from the general trade and objective requirements for standardized .
Be implemented in practice in order to make the principle of the single market, the EU further provides a reliable assessment of the product meets the basic requirements of the Directive stipulates that people commonly known as CE certification:
- The introduction of product evaluation modular concept, product evaluation process by the Evaluation Module, use the CE mark in accordance with the assessment procedures qualified products assessed;
- The introduction of a unified EU harmonized standards, quality management system standard (EN ISO 9000 series) and the assessment of institutional quality assurance standards (EN45000 series); between Member States - at the EU level assessment agencies and accreditation system and assessment agencies than on the mechanism;
- In the original countries to their own array of product testing and certification in the field to establish mutual recognition mechanism;
- Simplify between Member States, the quality system structure in the field (such as: measurement and calibration systems, testing laboratories, certification and inspection organization, recognized organizations) differences between the various sectors;
- Mutual recognition agreements, cooperation and technical assistance projects to promote international trade between Member States, the Member States and the EU countries outside the.
The purpose of the CE mark is to provide a way to practice is indeed feasible and flexible product conformity assessment, in order to meet the trend of global economic integration under the diversity of modern industrial production. Cater to product research and development, production, circulation stage (such as: design, proofing, production), check product evaluation module is divided into technical documentation, type testing, quality assurance, assessment completed by the producer or third party, as well as in practice.
Mark CE mark products in the market and put into service must meet the basic requirements of all applicable EU directives, select the appropriate product evaluation program for product evaluation qualified. All products are marked CE mark that already meet the EU directive, Member States must take active measures to ensure the free circulation in the single market, unless there is clear evidence that the product does not meet the basic requirements of applicable directives, or This product has not yet been existing Directive stipulates certain significant danger. Product affixed CE mark meaning what?
The significance of the CE mark is: CE mark affixed to the product has passed the appropriate conformity assessment procedures and / or the manufacturer's declaration of conformity, in line with the EU directive stipulates that as the product is allowed to pass into the European market . Industrial products relevant instructions to affix the CE mark, CE mark may not be listed for sale, affix the CE mark to market the product, found not to meet the safety requirements, and should be ordered to withdraw from the market, the continuing violation of the instructions to the relevant provisions of the CE mark , will be restricted or prohibited from entering the EU market or be forced to exit the market.
CE mark is not a mark of quality, it is a representative of the product has met a series of standards and directives of the European safety / health / environmental / health mark. All products sold in the EU should be mandatory marked with the CE marking.
--- This Source CE data network
2012-05-18
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