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Inhaltsverzeichnis
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Medizinproukte-VO
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Inhaltsverzeichnis
KAPITEL I: GELTUNGSBEREICH UND BEGRIFFSBESTIMMUNGEN
(Art. 1 - Art. 4)
KAPITEL II: BEREITSTELLUNG AUF DEM MARKT UND INBETRIEBNAHME VON PRODUKTEN, PFLICHTEN DER WIRTSCHAFTSAKTEURE, AUFBEREITUNG, CE-KENNZEICHNUNG, FREIER VERKEHR
(Art. 5 - Art. 24)
KAPITEL III: IDENTIFIZIERUNG UND RÜCKVERFOLGBARKEIT VON PRODUKTEN, REGISTRIERUNG VON PRODUKTEN UND WIRTSCHAFTSAKTEUREN, KURZBERICHT ÜBER SICHERHEIT UND KLINISCHE LEISTUNG, EUROPÄISCHE DATENBANK FÜR MEDIZINPRODUKTE
(Art. 25 - Art. 34)
KAPITEL IV: BENANNTE STELLEN
(Art. 35 - Art. 50)
KAPITEL V: KLASSIFIZIERUNG UND KONFORMITÄTSBEWERTUNG
(Art. 51 - Art. 60)
KAPITEL VI: KLINISCHE BEWERTUNG UND KLINISCHE PRÜFUNGEN
(Art. 61 - Art. 82)
KAPITEL VII: ÜBERWACHUNG NACH DEM INVERKEHRBRINGEN, VIGILANZ UND MARKTÜBERWACHUNG
(Art. 83 - Art. 100)
KAPITEL VIII: KOOPERATION ZWISCHEN DEN MITGLIEDSTAATEN, DER KOORDINIERUNGSGRUPPE MEDIZINPRODUKTE, FACHLABORATORIEN, EXPERTENGREMIEN UND PRODUKTREGISTER
(Art. 101 - Art. 108)
KAPITEL IX: VERTRAULICHKEIT, DATENSCHUTZ, FINANZIERUNG UND SANKTIONEN
(Art. 109 - Art. 113)
KAPITEL X: SCHLUSSBESTIMMUNGEN
(Art. 114 - Art. 123)
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