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21.08.2009 11:03
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Angewendete Richtlinien
Das Produkt erfüllt die Anforderungen der Richtlinie
93/42/EWG über Medizinprodukte.
Das Gerät entspricht den Normen für nicht invasive Blutdruck-
messgeräte EN 1060-1: 1995+A1:2002 und
EN 1060-3: 1997+A1:2005.
Das Gerät erfüllt die Anforderungen der elektromagnetischen
Verträglichkeit EN 60601-1-2:2001/A1:2004. Falls Sie Fragen
zur elektromagnetischen Verträglichkeit oder den gemessenen
Werten haben, wenden Sie sich bitte an unseren Service: 01805
633 633 (0,14 Euro/Minute aus dem deutschen Festnetz der
Telekom, abweichende Mobilfunknetzpreise möglich).
Das Gerät ist klassifiziert gemäß Typ B ( „Schutz gegen
elektrischen Schlag“).
Das Gerät wurde hergestellt im Jahr 2009
MEDION AG, 45307 Essen, Germany
Die Seriennummer des Gerätes befindet sich auf dem Typen-
schild.
37


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