The CE marking (Conformité Européenne) is a marking that identifies certain products in the European Union (EU) and the European Economic Area (EEA). CE certification confirms that a product meets EU-wide requirements for safety, health and environmental protection.
Here are some key aspects about CE certifications:
- Applicability of CE marking:
- CE marking is mandatory for a wide range of products, particularly those covered by an EU directive or regulation.
- Relevant EU directives:
- Various EU directives specify the requirements for specific product categories. Examples include the Machinery Directive, the Low Voltage Directive, the Medical Devices Directive and the Construction Products Regulation.
- Identification of old systems:
- The labeling requirement applies not only to new production lines, but also to existing systems.
- Attach CE marking:
- After successful conformity assessment and creation of the technical documentation, the manufacturer can affix the CE marking to the product or system.
- Keep documentation:
- The system operator must keep the technical documentation and other relevant documents for at least 10 years.
CE certification is an important step for manufacturers who want to distribute their products on the European market. The same also applies to the operation of production facilities. Compliance with CE requirements demonstrates conformity with EU standards and increases consumer confidence in the safety and quality of products.