Product description

CE certification is a compulsory certification in European Union countries. If the product does not have the CE mark, it will not be allowed to be sold in the European market.

CE marking: 
CE certification application process

1. Fill in the "Test Application Form" and provide technical information such as (specification.)
2. Quotation (the picture is not comprehensive, and the finished product estimate needs to be provided)
3. Payment 
4. Provide samples for testing. If it is not qualified, the company will be notified as soon as possible. Rectification and retesting.
5. Apply for the corresponding test report after passing the test 
6. Issue CE certificate

For example, CE directive standards cover a variety of directives for different products. For example, CE LVD (Low Voltage Directive) Low Voltage Directive, etc

The corresponding standards can be referred to as follows:

1. Safety of toys - Directive 2009/48/EU;
2. Mobile pressure equipment - Directive 2010/35/EU;
3. Restriction of hazardous substances in electrical and electronic equipment - Directive 2011/65/EU;
4. Construction Products - Regulation (EU) No. 305/2011;
5. Pyrotechnic products - Directive 2013/29/EU;
6. Recreational boats and personal waterboats - Directive 2013/53/EU;
7. Explosives for civil use - Directive 2014/28/EU;
8. Simple pressure vessels - Directive 2014/29/EU;
9. Electromagnetic compatibility - Directive 2014/30/EU;
10. Non-automatic weighing instruments - Directive 2014/31/EU;
11. Measuring instruments - Directive 2014/32/EU;
12. Lifts - Directive 2014/33/EU;
13. Equipment and protection systems for potentially explosive atmospheres - Directive 2014/34/EU;
14. Radio equipment - Directive 2014/53/EU;
15. Low pressure - Directive 2014/35/EU;
16. Pressure equipment - Directive 2014/68/EU;
17. Marine equipment - Directive 2014/90/EU;
18. Cableway installations - Regulation (EU) 2016/424;
19. Personal protective equipment - Regulation 2016/425;
20. Gas appliances - Regulation (EU) 2016/426;
21. Medical devices - Regulation 2017/745;
22. In vitro diagnostic medical devices - Specification (EU) 2017/746;