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39 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 338573_2001
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 Umgebun-
gen geeignet, die in dieser Gebrauchsanweisung aufgeführt
sind, einschließlich der häuslichen Umgebung. Bitte beach-
ten Sie dabei, dass tragbare und mobile HF-kommunikations-
einrich
tungen 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: Ergänzende An-
forderungen für elektromechanische Blutdruckmesssysteme)
und IEC 80601-2-30 (Medizinische elektrische Geräte Teil
2 – 30: Besondere Festlegungen für die Sicherheit einschließ-
lich der wesentlichen Leistungsmerkmale von automatisierten
nicht invasiven Blutdruckmessgeräten).
39


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