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particolari per quanto riguarda la compatibilità elet-
tromagnetica. Apparecchiature di comunicazione HF
mobili e portatili possono influire sul funzionamento di
questo apparecchio. Per informazioni più dettagliate,
rivolgersi all’Assistenza clienti oppure consultare la
parte finale delle istruzioni per l’uso.
L’apparecchio è conforme alla direttiva CE per i
dispositivi medici 93/42/CEE, alla legge sui dispo-
sitivi medici e alle norme europee EM1060-1 (Sfig-
momanometri non invasivi Parte 1: Requisiti gene-
rali), EN1060-3 (Sfigmomanometri non invasivi
Parte 3: Requisiti integrativi per sistemi elettro-
meccanici per la misurazione della pressione arte-
riosa) e IEC80601-2-30 (Apparecchi elettromedicali
Parte 2 30: Prescrizioni particolari relative alla sicu-
rezza fondamentale e alle prestazioni essenziali di sfig-
momanometri automatici non invasivi).
La precisione di questo misuratore di pressione è stata
accuratamente testata ed è stata sviluppata per una
lunga durata di vita utile. Se l’apparecchio viene uti-
lizzato a scopo professionale, è necessario effettuare
controlli tecnici con gli strumenti adeguati. Richiedere
informazioni dettagliate sulla verifica della precisione
all’indirizzo indicato del servizio assistenza.
54


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