Theme | Designation as notified body |
Target Audience | Conformity assessment bodies |
Products concerned | MD & IVD |
Documents mentioned |
MDR (EU) 2017/745 IVDR (EU) 2017/746 |
These MDCG guides (15 & 16) correspond to the forms to be completed by conformity assessment bodies when applying for designation as notified body under Regulation (EU) 2017/745 for medical devices and Regulation (EU) 2017/746 for in vitro diagnostic medical devices.