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Cet appareil est en conformité avec la norme européenne
EN60601-1-2 et répond aux exigences de sécurité spé-
ciales relatives à la compatibilité électromagnétique.
Veuillez noter que les dispositifs de communication HF
portables et mobiles sont susceptibles d’influer sur cet
appareil. Pour des détails plus précis, veuillez contacter
le service après-vente à l‘adresse ci-dessous.
L’appareil correspond à la directive européenne sur les
produits médicaux 93/42/EC, à la loi sur les produits
médicaux et aux normes européennes EN1060-1 (ap-
pareils de mesure non invasive de la tension artérielle
partie 1: exigences générales) et EN1060-3 (appareils
de mesure non invasive de la tension artérielle partie
3: exigences complémentaires pour systèmes électro-
mécaniques de mesure de la tension artérielle).
Si l’appareil est utilisé à des fins professionnelles ou
commerciales, conformément à « l’ordonnance sur les
produits médicaux », des contrôles techniques réguliers
doivent être effectués. Y compris en cas d’utilisation pri-
vée, nous vous recommandons de demander au fabricant
de procéder à un contrôle technique tous les 2 ans.
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