CS MEDICA Achieves MDR Classification, Setting New Standards in Substance-Based Medical Devices
Leading Healthcare Innovation with Stringent ComplianceCS MEDICA, a pioneer in MedTech specializing in pain management, autoimmune diseases, and stress-related disorders, has reached a significant regulatory milestone: · Class IIa Classification: Confirmed under Europe's Medical Device Regulation (MDR) for 3 substance-based medical devices with CBD under Rule 21. · Notified Body: A certification by BSI, the notified body (authority) that defines the classification and certifies the products, underscoring our stringent compliance and market readiness. Responding to Consumer