Medical Device Directive (MDD)

The Medical Device Directive (MDD) is a set of regulations in the European Union designed to ensure that medical devices, such as pacemakers or surgical tools, are safe and effective for patients. It outlines requirements for design, manufacturing, and testing, ensuring that devices meet high safety standards before they can be sold. Manufacturers must follow specific procedures to show compliance, and devices are classified based on their level of risk. The MDD aims to protect public health while facilitating innovation in medical technology.