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Cleansing instrument CE Certification Laboratory, Cleansing instrument CE Certification Cost
EU CE Certification Profile:
CE certification is the "main requirement" that constitutes the core of the European Directive. In the Resolution on New Methods of Technical Coordination and Standards of the European Community of 7 May 1985 (85/C136/01), the "main requirement" which needs to be used as the purpose of formulating and implementing the Directive has a specific meaning, that is, only products do not endanger the safety of human beings, animals and goods. All-round basic safety requirements, rather than general quality requirements, coordinate instructions only specify the main requirements, and general instructions are standard tasks.
What does the letter CE mean?
The "CE" sign in the EU market is a compulsory certification mark. If the products produced by enterprises within the EU or those produced by other countries want to circulate freely in the EU market, they must be affixed with the "CE" sign to show that the products meet the basic requirements of the EU Directive "New Approach to Technology Coordination and Standardization". This is a mandatory requirement of EU law for products.
What is the meaning of CE logo?
The meaning of CE logo is that the product with CE abbreviation is symbolized to indicate that the product with CE logo meets the main requirements of the relevant European Directive (Essential Requirements), and is used to confirm that the product has passed the corresponding conformity assessment procedures and the qualified declaration of the manufacturer, and is truly allowed to enter the market of EC. Pass for sale.
The relevant directives require industrial products with CE logo to be put on the market without CE logo. Products that have been put on CE logo to enter the market are not allowed to go on sale. If they find that they do not meet the safety requirements, they shall be ordered to withdraw from the market. If they continue to violate the relevant CE logo provisions of the directive, they will be restricted or forbidden to enter the EU market or be forced to withdraw from the market.
CE mark is not a quality mark, it is a mark representing that the product has met the safety/health/environmental protection/health standards and instructions of Europe. All products sold in the EU must be mandatory CE mark.
Why apply for CE certification? Necessity of applying for CE certification?
CE certification provides a unified technical specification for the trade of products in European markets and simplifies the trade procedures. In order to enter the European Union and the European Free Trade Area (EFTA), products of any country must be certified by CE and labeled with CE. Therefore, CE certification is the passport for products to enter the European Union and European Free Trade Area countries.
CE Certification indicates that the product has met the safety requirements stipulated in the EU Directive; it is a commitment of enterprises to consumers, which increases consumers'trust in the product; and products with CE logo will reduce the risk of sales in the European market. These risks include:
1. The risk of being detained and investigated by the Customs;
2. Risks to be investigated and dealt with by market supervision agencies;
3. The risk of being accused by peers for competitive purposes.
What are the benefits of applying for CE certification?
The EU's laws, regulations and coordination standards are not only numerous, but also very complex. Therefore, it is a wise move to obtain assistance from designated EU agencies, which is time-saving, labor-saving and risk-reducing.
Obtaining CE certificates from EU designated agencies can gain the trust of consumers and market supervisors.
It can effectively prevent the emergence of irresponsible accusations.
In the face of litigation, the CE certificate of the EU designated agency will become the technical evidence with legal effect.
In recent years, more and more CE signs have been used in the European Economic Area (European Union, European Free Trade Association member countries, except Switzerland) market. The goods added with CE marks indicate that they meet the requirements of a series of European directives, such as safety, health, environmental protection and consumer protection.
The scope of application of CE certification:
EU EU and EEA countries need CE logo. As of January 2013, there are 27 member states of EU EU. They are:
Austria, Belgium, Belgium, Denmark, Finland, Finland, Finland, France, Germany, Greece Greece, Ireland, Italy, Luxemburg Luxembourg, Netherlands, Portugal, Spain, Sweden, United Kingdom ) Britain, Estonia Estonia, Latvia Latvia, Lithuania Lithuania, Poland, Czech Republic, Slovakia Slovakia, Hungary Hungary, Slovenia Slovenia, Malta Malta, Cyprus, Romania, Romania and Bulgaria Bulgaria.
Three EFTA member countries: Iceland Iceland, Liechtenstein Liechtenstein, Norway.
Semi-EU countries: Turkey Turkey.
What information should CE certification prepare? Technical documents to be prepared for CE certification?
1. The name and address of the manufacturer (EU Authorized Representative (EU Authorized Agent) AR, the name and model of the product, etc.
2. Instructions for the use of products;
3. Safety design documents (including key structural drawings, which can reflect climbing distance, clearance, insulation layer number and thickness);
4. Technical conditions (or enterprise standards) of products and establishment of technical data;
5. Principle diagrams, block diagrams and circuit diagrams of products and electrical appliances.
6. List of key components or raw materials (please select products with European certification marks);
7. Testing Report;
8. Certificates issued by NB, the EU Authorized Certification Authority (for modes other than mode A);
9. Certificate of product registration in EU (for some products such as Class I medical devices, ordinary IVD in vitro diagnostic medical devices);
1) Except as specified, the above information
2) For applications for various types of products, please provide information on each type separately.
3) If you apply for a series of products, please attach the similarities and differences between different models of the products.
ZKT since was established, grasps "the patient, careful, professional, efficient" service concept to whole-hearted service every customer, and get the support of numerous customers and international institutions, and any, the company has with the TUV rheinland, TUV she, SGS, Intertek Intertek, KTC BV, American UL, TIMCO, South Korea, India BIS, agencies and institutions authorized certificate report including the United States, Britain, Germany, France, Italy, Japan, South Korea, China, Taiwan and Hong Kong area, many countries and regions in recognition, with super international credibility and influence.
ZKT test project
CE, RoHS, REACH, ERP, tuv-mark, GS, VDE, e-mark, EN71, PAHS, LFGB, etc.
China CCC, CQC, the quality inspection report, Japan PSE, VCCI and TELEC, Taiwan NCC, the BSMI, such as South Korea KC, KCC Singapore PSB PVOC, Saudi Arabia SASO, Kenya, Nigeria SONCAP, India BIS.
FCC, CEC, UL, ETL, ASTM, Energy - Star, FDA, CPSIA, CSA, IC, NOM, MET, etc.
C - TICK, SAA, RCM, GEMS, etc.
ISO 9001 quality management system
ISO14001 environmental management system
OHSAS18001 (GB/T28001) occupational health and safety management system
ISO/TS16949 automobile distribution quality management
ISO13485 medical device quality management system
SA8000 (BSCI) social responsibility
ISO/iec 20000 (ITSM) IT factory system certification
ISO/iec 27000 (ISMS) information security management system
Other certifications (international CB, ICE, UN38.3, MSDS, WEEE, aaa credit rating, etc.).