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Description des symboles utilisés dans ce
livret ou sur l’étiquette du conditionnement
Avertissements
Le texte reré par un symbole de
marquage doit être lu avant d’utiliser le
produit.
Fabricant
Le produit est élaboré par le fabricant
dont
le nom et l’adresse gurent à côté
du symbole. Indique le fabricant du
dispositif médical,
tel que déni dans les directives de
l’UE 90/385/CEE, 93/42/CEE et 98/79/CE.
Marque CE
Le produit est conforme à la directive de
l’UE sur les dispositifs médicaux 93/42/
CEE. Le nuro à quatre chires indique
l’identication de l’organisme notié.
Déchets électroniques (DEEE)
Recyclez vos aides auditives, accessoires
ou batteries et piles conformément aux
réglementations locales ou renvoyez-les
à votre audioprotsiste en vue de leur
mise au rebut.
Équipements électroniques couverts par
la Directive 2012/19/UE sur les déchets et
les équipements électriques (DEEE).
E2105
Marque de conformité réglementaire
(RCM)
Le produit est conforme aux exigences de
curité électrique, de CEM et de spectre
radio relatives aux produits fournis au
marché australien ou néo-zélandais.
48


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