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c
Lecteur de glycémie: ce produit répond à la Directive Européenne 1999/5/CE
concernant les équipements hertziens et les équipements de télécommunication
(R&TTE).
C
Lecteur de glycémie: ce produit répond aux exigences de la Directive Européenne
98/79/CE relative aux dispositifs médicaux de diagnostic in vitro.
C
Autopiqueur et cartouche de lancettes:
ce produit répond aux exigences de la Directive Européenne 93/42/CEE relative aux
dispositifs médicaux.
F
Ce produit répond aux exigences de la section 15 de la réglementation FCC et à la
norme RSS-210 d’Industrie Canada.
La marque de conformité signifie que le produit est conforme aux normes en vigueur et
établit un lien de traçabilité entre l’appareil et le fabricant, l’importateur, ou tout
mandataire chargé de l’introduction de l’appareil sur les marchés australien et néo-
zélandais, et responsable à ce titre de la conformité aux normes correspondantes.
La signification des autres symboles est indiquée dans le manuel d’utilisation et les notices fournies avec
les composants dans l’emballage.
Conforme aux directives de l’alliance Continua Health Alliance
Certifié par l’organisation USB Implementers Forum
man_07419350001_01_FR.indb 139 20.05.2015 17:27:46
141


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