DECRETO 13 novembre 2017 - Modifica dell'elenco delle officine che alla data del 31 agosto 2017 risultano autorizzate alla produzione di presidi medico-chirurgici. (17A08130)
IL DIRETTORE GENERALE dei dispositivi medici e del servizio farmaceutico Visto l'art. 189 del regio decreto 27 luglio 1934, n. 1265, recante «Approvazione del testo unico delle leggi sanitarie» e successive modificazioni;
Visto il decreto del Presidente della Repubblica 6 ottobre 1998, n. 392, «Regolamento recante norme per la semplificazione dei procedimenti di autorizzazione alla produzione ed alla immissione in commercio di presidi medico-chirurgici, a norma dell'art. 20, comma 8 della legge 15 marzo 1997, n. 59» e, in particolare, l'art. 3, comma 4, ai sensi del quale l'elenco delle officine autorizzate alla produzione e' pubblicato nella Gazzetta Ufficiale della Repubblica italiana;
Visto il decreto direttoriale del 15 febbraio 2006, concernente la «Specificazione dei contenuti della domanda di autorizzazione alla produzione di presidi medico-chirurgici»;
Visto il decreto legislativo 30 marzo 2001, n. 165 e successive modificazioni ed integrazioni;
Vista la legge n. 172 del 13 novembre 2009, recante l'istituzione del Ministero della salute;
Vista la legge 7 agosto 1990, n. 241 e successive modifiche;
Visto il decreto direttoriale del 29 settembre 2017, recante «Elenco delle officine che alla data del 31 agosto 2017 risultano autorizzate alla produzione di presidi medico-chirurgici», pubblicato nella Gazzetta Ufficiale - Serie generale - n. 238 dell'11 ottobre 2017;
Rilevata l'omessa identificazione nel suddetto decreto, per mero errore materiale, dell'officina di produzione Ecolab Production Italy S.r.l., via Grandi n. 9/11 - 20089 Rozzano (Milano);
Ritenuto di dover, pertanto, rettificare il decreto direttoriale del 29 settembre 2017 al fine di assicurare integralmente l'adempimento previsto dal menzionato art. 3, comma 4 del decreto del Presidente...
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