What are the specific obligations of importers regarding CE marked products?

10 steps to success: 1. Determine intended purpose 2. Determine classification 3. Determine conformity assessment routes 4. Comply with conformity requirements. Mar 13, 2025 ... Electronic products sold in the EU must have a CE Mark. Learn about the CE Mark requirements and compliance standards required for ... They signify that products sold in the EEA have been assessed to meet high safety, health, and environmental protection requirements. Products with the CE mark (“Communité Européenne”) show compliance with the harmonized European Norm (hEN) standards. CE marked products can be used throughout ... Feb 23, 2021 ... The CE-marking is a clear indicator of a product's compliance with EU legislation. It is thus not an indication the product was produced in the EEA or Turkey. CE marking is required for all in vitro diagnostic (IVD) devices sold in Europe. CE marking indicates that an IVD device complies with the European In-Vitro ... What is CE marking? CE marking indicates the manufacturer's claim that a product meets the essential requirements of all relevant European directives and/or ... The Conformité Européene (CE) Mark is defined as the European Union's (EU) mandatory conformity marking for regulating the goods sold within the European ... If a product has a CE marking affixed, it also indicates that the manufacturer has performed a conformity assessment and set up the appropriate technical ... Jan 15, 2024 ... CE marking is not required for prototype devices. If your product is in the design, prototype or development phase and isn't yet ready for the ...