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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 pro-
duits médicaux 93/42/EC, à la loi sur les produits médicaux
et aux normes européennes EN1060-1 (appareils de me-
sure 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 com-
merciales, conformément à « l’ordonnance sur les produits
médicaux », des contrôles techniques réguliers doivent être
effectués. Y compris en cas d’utilisation privée, nous vous
recommandons de demander au fabricant de procéder à
un contrôle technique tous les 2 ans.
24


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