[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"norm-eurlex-mdr-erwgr-14-de":3},{"law":4,"norm_id":14,"norm_key":15,"slug":16,"title":17,"chapter":18,"content":19,"enriched_content":20,"hierarchy":21,"neighbors_before":22,"neighbors_after":32,"citing_decisions":42,"is_thin":43},{"abbreviation":5,"title":6,"source_type":7,"jurisdiction":8,"document_kind":9,"language":10,"attribution":11,"version_date":12,"source_url":13},"mdr","über Medizinprodukte, zur Änderung der Richtlinie 2001\u002F83\u002FEG, der Verordnung (EG) Nr. 178\u002F2002 und der Verordnung (EG) Nr. 1223\u002F2009 und zur Aufhebung der Richtlinien 90\u002F385\u002FEWG und 93\u002F42\u002FEWG des Rates","eurlex","eu","regulation","de","© Europäische Union, https:\u002F\u002Feur-lex.europa.eu","2025-02-11","https:\u002F\u002Feur-lex.europa.eu\u002Flegal-content\u002FDE\u002FALL\u002F?uri=CELEX:32017R0745",17345262,"ErwGr. 14","erwgr-14",null,"Erwägungsgründe","Die Anforderungen im Sinne der Richtlinie 2002\u002F98\u002FEG des Europäischen Parlaments und des Rates (10) sollten weiterhin gelten.","MDR - Erwägungsgründe - ErwGr. 14\n\nDie Anforderungen im Sinne der Richtlinie 2002\u002F98\u002FEG des Europäischen Parlaments und des Rates (10) sollten weiterhin gelten.",{},[23,26,29],{"norm_key":24,"title":17,"slug":25},"ErwGr. 13","erwgr-13",{"norm_key":27,"title":17,"slug":28},"ErwGr. 12","erwgr-12",{"norm_key":30,"title":17,"slug":31},"ErwGr. 11","erwgr-11",[33,36,39],{"norm_key":34,"title":17,"slug":35},"ErwGr. 15","erwgr-15",{"norm_key":37,"title":17,"slug":38},"ErwGr. 16","erwgr-16",{"norm_key":40,"title":17,"slug":41},"ErwGr. 17","erwgr-17",[],true]