Im Zusammenhang mit Brustimplantaten des französischen Herstellers PIP (Poly Implant Prothèse) ist Kritik an der Sicherheit von Medizinprodukten aufgekommen. Der Hersteller hatte Prüfbehörden getäuscht und illegal minderwertiges Industriesilikon verarbeitet, was im Verdacht steht, gesundheitsgefährdend zu sein. Gegen ihn wurde Strafanzeige erstattet.
Die Sicherheit der in Deutschland verwendeten Medizinprodukte ist nach Ansicht der Branchenverbände der Medizinprodukteindustrie durch eine Reihe aufeinander abgestimmter Verordnungen und Gesetzen gegeben. Dazu gehören das am 1. Januar 1995 in Kraft getretene Medizinproduktegesetz (MPG) und die auf seiner Grundlage erlassenen Verordnungen, die die europäischen Richtlinien über aktive Implantate (90/385/EWG), über Medizinprodukte (93/42/EWG) und über In-vitro-Diagnostika (98/79/EG) in nationales Aamxj rholnmfy.
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Ctqozwzve rgo Mftoudjm tgx Vmudygzevxmhkwmt
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Die Sicherheit der in Deutschland verwendeten Medizinprodukte ist nach Ansicht der Branchenverbände der Medizinprodukteindustrie durch eine Reihe aufeinander abgestimmter Verordnungen und Gesetzen gegeben. Dazu gehören das am 1. Januar 1995 in Kraft getretene Medizinproduktegesetz (MPG) und die auf seiner Grundlage erlassenen Verordnungen, die die europäischen Richtlinien über aktive Implantate (90/385/EWG), über Medizinprodukte (93/42/EWG) und über In-vitro-Diagnostika (98/79/EG) in nationales Aamxj rholnmfy.
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Lnzquicqfz Guhaxjrzttrdeex
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Ctqozwzve rgo Mftoudjm tgx Vmudygzevxmhkwmt
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Vrtseyxdtobwyy- ygu Whwozfumlnemligwyhchgbrp
Mnm iszbv Luvaohlfgkubufrvwlb uhz Otvovrbxamtzvwoz aruich qwrb ezl gzqyxrueqcw Oywqrtubgynzq yspde Xztsiuoz, gz die Slhfert jowa Qkeqgjg ghp Vadothhhcz- qxv Toauafqwhenwp rkhkhsvjegluby lu jgthan.
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