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235 DE/AT/CH
Bitte beachten Sie dabei, dass tragbare und mobile HF-Kommunikationseinrichtungen dieses
Gerät beeinflussen können. Genauere Angaben können Sie unter der angegebenen Kunden-
service-Adresse anfordern oder am Ende der Gebrauchsanweisung nachlesen.
Das Gerät entspricht der EU-Richtlinie für Medizinprodukte 93/42/EEC, dem Medizin-
produktegesetz und der Norm EN ISO 80601-2-61 (Medizinisch elektrische Geräte −
Besondere Festlegungen für die grundlegende Sicherheit und die wesentlichen Leistungs-
merkmale von Pulsoximetern für den medizinischen Gebrauch).
Wir bestätigen hiermit, dass dieses Produkt der europäischen RED Richtlinie 2014/53/EU
entspricht. Die CE-Konformitätserklärung zu diesem Produkt finden Sie unter:
www.sanitas-online.de/web/de/landingpages/cedeclarationofconformity.php
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