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Measurements were performed using a salbutamol solution with a "Next Generation Impactor" (NGI).
The diagram may therefore not be applicable to suspensions or highly viscous medications. You can
obtain more detailed information from the manufacturer of your medication.
NOTICE
If the device is not used according to the specifications, it may not work correctly! We reserve the right
to make technical changes to improve and develop the product.
This device and its atomiser set conform with the European standard EN 60601-1-2 (Group 1, Class
B, in accordance with CISPR 11, IEC 61000-3-2, IEC 61000-3-3, IEC 61000-4-2, IEC 61000-4-3,
IEC 61000-4-4, IEC 61000-4-5, IEC 61000-4-6, IEC 61000-4-8, IEC 61000-4-11) and are subject to par-
ticular precautions with regard to electromagnetic compatibility.
13. GUARANTEE / SERVICE
More information on the guarantee and guarantee conditions can be found in the guarantee leaflet
supplied.
Notification of incidents
For users/patients in the European Union and identical regulation systems (EU Medical Device Regu-
lation (MDR) 2017/745), the following applies: If a major incident occurs during or through use of the
product, notify the manufacturer and/or their representative of this as well as the respective national
authority of the member state in which you are located.
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