The CE Marking Is a crucial certification for medical devices sold within the European Union (EU) and European Economic Area (EEA). This mark is not only a legal requirement but also serves as a symbol of safety, quality, and regulatory compliance. CE marking assures that a product meets the strict https://online-cancer-consultatio08530.blogdun.com/32012702/ce-marking-for-medical-devices-ensuring-compliance-and-market-access-in-europe