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Déclaration de conformité:
Le fabricant déclare par la présente que cet appareil est conforme aux
normes suivantes:
IEC 60601-1: 2005 + A1: 2012,
IEC60601-1-2: 2014,
IEC60601-1-11: 2010, ISO 80601-2-61: 2011 et est conforme aux dis-
positions de la directive du Conseil MDD93 / 42 / CEE
10. LEGENDA DEI SIMBOLI
FRANÇAIS
Á conserver dans un
endroit frais et sec
Dispositif médical conforme
à la directive 93/42 / CEE
Suivez les instructions
d'utilisation Fabricant
Numéro de série Date de fabrication
Code produit Appareil de type BF
Numéro de lot Á conserver à l’abri
de la lumière du soleil
Disposition DEEE
Attention: lisez attentivement
les instructions
(avertissements)
%SpO2Saturation pulsée
en oxygène PI Indice de perfusion
bpm
Fréquence de pouls
(battements par
minute)
Tension de batterie faible
15


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