View source for Category:EU Regulation

Pages in this category relate to EU regulatory frameworks governing medical devices and in vitro diagnostic devices, including MDR (EU 2017/745) and IVDR (EU 2017/746).

== Documents ==

{{#ask: [[Category:EU Regulation]] [[Status::+]]
| ?Document name = Name
| ?Status = Status
| ?Area of validity = Region
| ?Version = Version
| format=table
| headers=show
| limit=50
| sort=Status
}}