The EU Commission and Member States have created country language tables in order to provide an overview which language requirements are required by each Member State for following items:
– Labelling & Instruction for Use (patient, lay user or professional user)
– Implant card
– Declaration of conformity
– Field safety notice
– Graphical user interface, e.g. (mobile) apps (patient, lay user or professional user)
The tables were provided for both, MDR and IVDR. See here for more info on MDR EU 2017/745 and IVDR EU 2017/746.