Medical Device Regulation (EU) 2017/74 Course
Medical Device Regulation (EU) 2017/74 Course
Aug 17, 2021
medicaldevicehq.com
🚨 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
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