ch_5Level 1
Chapter V - Classification and Conformity Assessment
Chapter V of the EU Medical Device Regulation sets out the rules for classifying medical devices into classes I, IIa, IIb and III based on risk, and details the conformity
GET
/api/v1/systems/reg_mdr/nodes/ch_5Hierarchy Explorer
Cross-system equivalences0
No cross-system equivalences mapped for this node.