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37 DE/AT/CH
Fordern wir Sie zur Übersendung des defekten Blutdruck-
messgeräts auf, ist das Produkt an folgende Adresse zu
senden:
NU Service GmbH
Lessingstraße 10 b
89231 Neu-Ulm
DEUTSCHLAND
IAN 322244
Dieses Gerät entspricht der europäischen Norm EN 60601-1-2
(Übereinstimmung mit CISPR 11, IEC 61000-4-2,
IEC 61000-4-3, IEC 61000-4-8) und unterliegt besonderen
Vorsichtsmaßnahmen hinsichtlich der elektromagnetischen
Verträglichkeit. Das Gerät ist für den Betrieb in allen Umge-
bungen geeignet, die in dieser Gebrauchsanweisung aufge-
führt sind, einschließlich der häuslichen Umgebung. Bitte
beachten Sie dabei, dass tragbare und mobile HF-kommu-
nikationseinrichtungen dieses Gerät beeinflussen können.
Das Gerät entspricht der EU-Richtlinie für Medizinprodukte
93/42/EEC, dem Medizinproduktegesetz und den Normen
EN 1060-3 (nicht invasive Blutdruckmessgeräte Teil 3: Ergän-
zende Anforderungen für elektromechanische Blutdruckmess-
systeme) und IEC 80601-2-30 (Medizinische elektrische
Geräte Teil 2 – 30: Besondere Festlegungen für die Sicher-
heit einschließlich der wesentlichen Leistungsmerkmale von
automatisierten nicht invasiven Blutdruckmessgeräten).
37


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