Die EU Medizinprodukte-Verordnung war aufgrund des Brustimplantate-Skandals von 2012 übererarbeitet worden. Damals kamen zahlreiche Frauen durch Implantate mit Handwerker-Silikon zu Schaden. Ab heute müssen Medizinprodukte deutlich schärfere Zulassungsbedingungen erfüllen und alte Zertifikate bleiben nur
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