CE certification requirements:
1. The product must not interfere with health, does not jeopardize the environment and consumers, can be circulated on the market. 2. Products that are legally marketed in one EU country can also be sold in other member states. By labeling a product with the EU CE mark, the manufacturer indicates that the product is in full compliance with the relevant provisions of the EU Directive. If permitted by the regulations, the CE marking can also be displayed on the packaging or accompanying documents. The EU CE mark is not a test mark, but simply indicates that the manufacturer declares that its products comply with all relevant regulations. Currently there are a variety of conformity assessment model to mark compliance with the basic provisions, these provisions may involve several units, such as manufacturers, importers and distributors. If you want to apply for CE marking, show that the product complies with the standard, or to find a third-party testing organization to issue certificates. Not all products need to be CE-marked for trading in the EEA; only product categories that comply with relevant directives or regulations need (and are allowed) to bear the CE marking, and most CE-marked products can only be controlled by the manufacturer's internal production, without independent inspection of the product's compliance with EU regulations. CE marking can be done in the case of products with little risk of self-certification, high-risk products to be tested by the designated certification body, in these cases, CE marking requires the announcement of the organization's registration number.Second, the need for CE marking of the country:
CE marking of certain products within the European Economic Area (EEA; 28 member states of the European Union and the European Free Trade Association countries of Iceland, Norway and Liechtenstein), as well as Switzerland and Turkey is mandatory. Manufacturers of products manufactured in the EEA and importers of goods manufactured in other countries must ensure that CE-marked products comply with the standards.Three, why is the EU CE mark important?
The relevant directives require the affixing of the CE marking of industrial products, there is no CE marking, may not be marketed and sold, has been affixed to the CE marking of the products into the market, found to be inconsistent with the safety requirements, to be ordered to retrieve from the market, continued violation of the directives related to the CE marking of the provisions of the EU market will be restricted or prohibited from entering the market or forced to withdraw from the market.Four, what is the CE certification directives and standards:
Thousands of electronic products on the market, CE certification needs to be done to certify that the directive and test standards are different, such as the Machinery MD Directive, 2006/42/EC is its directive number, the corresponding directive there are a lot of different EN standards, we are on a common Several different products CE marking directives and standards to do a simple statistics.Fifth, the European Union CE certification covers the following product categories:
1. machinery and equipment (MD) 2. potentially explosive atmospheres in machinery (ATEX) 3. electrical equipment (LVD) 4. electronic equipment: household and industrial (EMC) 5. construction products (CPR) 6. ) 6. Medical Devices (MD) 7. Personal Protective Equipment (PPE) 8. Pressure Equipment (PED) 9. Radio Equipment (RED) 10. Toys (Toys) 11. Restriction of the Use of Certain Substances (RoHS) 12. Other Consumer ProductsVI. What information is needed to do CE marking:
1. Customer application form (English: product name CE marking, model CE marking, applicant/manufacturer address). 2. Product model and detailed technical parameters 3. Detailed pictures of components and overall structure 4. Electrical schematic diagrams (electrical products) 5. Mechanical assembly drawings and drawings of key components 6. Nameplate (font, CE symbol). 7. Product manuals, installation, maintenance (English). 8. Parts list (product name CE certification, manufacturer).Seven, the enterprise manufacturer to find a third testing organization to apply for CE certification process:
1. Manufacturers and testing organizations (hereinafter referred to as the laboratory) to make a preliminary oral or written application. 2. The applicant to fill out the CE-marking application form, the application form, samples, electrical schematic diagrams, product specifications sent to the laboratory (prepare 1 to 2 samples). 3. The laboratory to determine the test standards and test items and quotation. 4. The applicant to confirm the offer, and send samples and related technical documents to the laboratory. 5. Applicants provide technical documents. 6. The laboratory issued a fee notice to the applicant, the applicant in accordance with the fee notice to pay the certification fee. 7. Laboratory product testing and review of technical documents.Eight, technical document review include:
a. Whether the document is perfect. b. Whether the document is written in the official language of the European **** body (English, German or French). 9. If the technical documentation is inadequate or not in the required language, the Laboratory will notify the applicant to improve it. 10. If the test fails, the Laboratory will promptly inform the applicant to improve the product until it passes the test, and the applicant should make changes to the technical data in the original application to reflect the actual situation after the changes. 11. Article 9, 10 of the rectification costs involved, the laboratory will issue a supplementary fee notice to the applicant. 12. The applicant will be required to pay the cover charge in accordance with the Supplemental Charge Notice. 13. The laboratory provides the applicant with the test report or technical file (TCF), and the CE Certificate of Conformity (COC), and CE marking. 14. The applicant signed a self-declaration of CE assurance, and CE marking attached to the product.Nine, the cost of CE certification in the European Union is probably:
DC ordinary high-voltage products to do CE-LVD and CE-EMC, CE certification costs about 2500 yuan, cycle 7-10 working days.Ten, CE certification requires factory review? Is there any other follow-up costs?
CE certification and CCC, UL and other certifications are not the same, only for the sample safety testing, so there is no factory review, if the product does not change, the test standards have not been updated, there will be no other follow-up costs.Xi, CE certification time how long?
At present, the conventional product CE certification test two parts, one is the EMC electromagnetic compatibility test, the other LVD safety test, the general product CE testing time for about 10 days.Twelve, CE certification report is valid for how long?
CE certification has no hard validity time limit, generally can always be effective, but in the following cases, the product needs to be re-certified or the certificate needs to be updated: 1: the previous certification of the directives used by the new directives to replace the 2: certified products to make significant changes 3: the product into the market after the emergence of safety issues, the certificate was canceled by the official.