🚨 New Video: Essential Definitions in EU MDR Article 2 🚨 In this episode, we’re diving deeper into the European Medical Device Regulation (EU MDR) 2017/745, focusing on key terms that every regulatory professional should know: 🔹 Generic Device Group – How devices are classified based on similar purposes and technology 🔹 Single-Use Device – Understanding devices designed for one-time use only 🔹 Falsified Device – Recognizing devices that falsely represent their identity or CE marking 🔹 Proc