The CE Mark certification is a critical requirement for medical devices intended for sale in the European Economic Area (EEA). This mark signifies that a product complies with the EU's Medical Device Regulation (MDR) or In Vitro Diagnostic Regulation (IVDR), meeting stringent health, safety, and environmental protection standards. To earn CE Mark certification, manufacturers must thor... https://paragoncertifications.com/medical-devices-ce-mark-certifications/