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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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