The CE Mark (Conformité Européenne) is a critical certification for medical devices sold in the European Union (EU) and the European Economic Area (EEA). It signifies that a product meets the stringent health, safety, and environmental standards set by the European regulatory authorities. This mark is not only a legal https://mydirectorys.com/listings12981813/ce-marking-for-medical-devices-a-comprehensive-guide-to-compliance-in-the-european-market