MDR 2017/745 Specialist EU MDR compliance patterns for medical device classification, technical documentation, and clinical evidence. --- Table of Contents - Device Classification Workflow - Technical Documentation - Clinical Evidence - Post-Market Surveillance - EUDAMED and UDI - Reference Documentation - Tools --- Device Classification Workflow Classify device under MDR Annex VIII: 1. Identify device duration (transient, short-term, long-term) 2. Determine invasiveness level (non-invasive, body orifice, surgical) 3. Assess body system contact (CNS, cardiac, other) 4. Check if active device…