What happens if a CE marked product is used outside of its intended purpose?

Dec 23, 2020 ... The CE marking was granted on December 22, 2020 to CARMAT's total artificial heart system as a bridge to transplant in patients suffering from end-stage ... Apr 26, 2023 ... CE is an abbreviation of the French “Conformité Européenne”, which means “European Conformity”. Countries within the European Economic Area (EEA) ... Jun 28, 2023 ... What is CE Marking? CE marking is a conformity marking that indicates a product has been assessed as meeting essential health, safety, and ... 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 ... Oct 5, 2015 ... The application of CE mark enables Novocure to distribute the second generation Optune system in the European Union and Switzerland. Novocure ... A mark required for many products that must be assessed, before being placed on the market, to meet EU safety, health and environmental protection ... We are regulatory professionals who guide on specific requirements that must be met and obtain the medical device CE Marking. Nov 24, 2013 ... CE marking a four-digit number. The CE marking four-digit number that is displayed next to the CE mark on some medical devices is the Notified ... Nov 3, 2024 ... The CE marking under the European Accessibility Act (EAA) confirms that a product meets EU standards for accessibility, in addition to safety, ... The rules for affixing UKCA or CE marking to a product are the same. In most cases, businesses must apply the UKCA or CE marking to the product's surface or ...