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ELECTROMAGNETIC COMPATIBILITY
This device was designed to satisfy the currently required requisites for electromagnetic
compatibility (EN 60601-1-2:2015). Electro-medical devices require particular care during
installation and use relative to EMC requirements. Users are, therefore, requested to
install and/or use these devices following the manufacturer's specifications. There is a
risk of potential electromagnetic interference with other devices. RF mobile or portable
radio and telecommunications devices (mobile telephones or wireless connections) can
interfere with the functioning of electro-medical devices. For further information, visit the
manufacturer's website. The Device may be subject to electromagnetic interference if
other devices are used for specific diagnosis or treatments. The manufacturer reserves the
right to make technical and functional modifications to the product with no prior warning.
DEVICE DISPOSAL
In compliance with the Directive 2012/19/EC, the symbol printed on the device shows
that the device to be disposed of is considered waste and must therefore be an item
of ''differentiated collection''. Consequently, the user must take it (or have it taken)
to the designated collection sites provided by the local authorities, or turn it in to the
dealer when purchasing an equivalent new device. Differentiated waste collection and
the subsequent treatment, recycling and disposal procedures promote the production of
devices made with recycled materials and limit the negative effects on the environment
and on health caused by potential improper waste management. Unauthorised disposal
of the product by the user shall result in the application of administrative penalties, as per
article 50 and the subsequent revisions of Italian Legislative Decree no. 22/1997.
Aérosol à compresseur pour utilisation pédiatrique
Nous vous remercions pour votre achat et la confiance que vous nous accordez.
Nous avons pour objectif l'entière satisfaction de nos clients en leur offrant des produits
à l'avant-garde dans le traitement des maladies des voies respiratoires.
Veuillez lire
attentivement ces instructions et les conserver pour de futures consultations. Veuillez
médical à usage domestique pour pulvériser et administrer des médicaments prescrits et
recommandés par votre médecin qui a évalué les conditions générales du patient.
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Appareil pour aérosol
(unité principale)
A1 - Interrupteur
A2 - Prise d'air
A3 - Filtre à air
A4 - Porte-ampoule
A5 - Prise d'alimentation
A6 - Câble d'alimentation
avec bloc d’alimentation
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Tube de raccordement
(unité principale / ampoule)
Содержание Clenny A
Страница 51: ...49 v A A1 A2 A3 A4 5 A6 B C C2 1 6 Clenny A 2ME 2 C6 1 C6 2 C6 3 C6 4 C7 1 12 C8 1 12 D 1 6...
Страница 52: ...50 1 L A5 2 C6 1 3 C6 3 C6 1 4 400 93 42 CE...
Страница 53: ...51 1 SoftTouch CLENNY A 2ME 2 C6 4 MAX C6 4 MAX Clenny A 2ME MAX 1 1 12 5 A1 6 7 1 12...
Страница 55: ...53 A3 II EN 10993 1 93 42 EEC CE 1907 2006 CE 93 42 CEE IP21 12 BF ON OFF...
Страница 57: ...55 k...
Страница 58: ...56 EN 60601 1 2 2015 2012 19 CE 50 22 1997...
Страница 59: ...57 A A1 A2 A3 A4 A5 A6 B C C2 Clenny A 2ME C6 2 C6 1 C6 2 C6 3 C6 4 C7 12 1 12 1 C8 D 6...
Страница 60: ...58 A5 L 1 C6 1 2 C6 1 C6 3 3 4 400 42 93...
Страница 61: ...59 12 1 Soft Touch CLENNY A 2ME 2 C6 4 MAX C6 4 MAX Clenny A 2ME MAX A1 5 6 B 7 12 1...
Страница 64: ...62 A3 II EN10993 1 EEC 93 42 CE 1907 2006 CE CEE 93 42 IP21 12 FB ON OFF...
Страница 65: ...63...
Страница 66: ...64 CE 19 2012 CE 19 2012 EN 60 60601 1 2 2015 EMC RE...
Страница 67: ...65 5 MEMO MEMORANDUM NOTIZEN NOTAS...