Article 103 establishes the Medical Device Coordination Group (MDCG) composed of Member State representatives + Commission, with expert panels and EU reference laboratories supporting the Article 54 consultation procedure + Article 55 scrutiny mechanism + clinical evaluation guidance + class-up evaluation. Articles 104-108 detail expert-panel + reference-laboratory roles.
The graph holds this control, the 0 it maps to, and the evidence behind each claim, over MCP and REST.