GB
12
14.
Using the device in environmental conditions different than those indicated in this manual may harm seriously the safety and
the technical characteristics of the same;
15.
The materials used to contain the drugs are made with highly stable thermoplastic polymers that are resistant against
chemicals. Such materials were tested with commonly used drugs (Salbutamol, Beclametasone dipropionate, Acetylcysteine,
Budesonide, Ambroxol) and no interaction phenomenon was observed. Interactions cannot however be excluded given the
variety and the continuous evolution of the drugs that are used. Remember to:
To consume the drugs as quickly as possible after opening its package;
To avoid keeping the drug in the tray-like container for too long and to clean it immediately after every application;
If the tray-like container presents any abnormal situation (such as softening or cracks), do not introduce any solution and
do not proceed with the inhalation. Contact the technical service and describe the methods and type of drugs used.
16.
Remember to:
Only use this device with medicines prescribed by your doctor;
Carry out the treatment only using the accessory indicated by the doctor according to the pathology.
Under certain failure conditions the temperature of the casing may become hot and there may be a risk
of burns if you touch those parts. In any case, the temperatures do not exceed the limit of 105°C (ref.
Interpretation Sheet IEC 60601-1).
TECHNICAL CHARACTERISTICS
Model
EOLO
NEBULIZER
Typology (MDD 93/42/EEC)
Class IIa Medical device
Power Feeding
230V ~ / 50 Hz
Power Consumption
170 VA
Fuse
F 1 x 1.6A L 250V
Max Pressure
250 kPa (2.5 Bar)
Max Air Flow
14 l/min
Operating Pressure
110 kPa (1.1 Bar)
Operating Air Flow
5.0 l/min a 110 kPa
Neb-Rate (with 4ml of 0.9% NaCl solution)
0.40 ml/min with 4ml of 0.9% NaCl solution
MMAD
2.44 µm
GSD
2.87
Weight
1.65 Kg
Size
148 x 223 (h) x 124 (h)
Noise Level (measured as specifications of EN 13544-1)
Approx. 55dB (A)
Duty Cycle (to 40°C and 110% operating voltage)
Non-Stop Operated
Min Capacity Nebulizer
2ml
Max Capacity Nebulizer
6ml
Working Condition
Room temperature:
5 ÷ 40 °C
Room humidity percentage:
10 ÷93 % RH
Atmospheric pressure:
700 ÷ 1060 hPa
Conservation condition and Transport
Room temperature:
- 25 ÷70 °C
Room humidity percentage:
0 ÷ 93% RH
Atmospheric pressure:
500 ÷ 1060 hPa
The manufactured cannot be held liable for accidental or indirect damages should the device be
modified, repaired without authorization or should any of its component be damaged due to accident
or misuse. Any minimal modification / repair on the device voids the warranty and does not guarantee
the compliance with the technical requirements provided by the MDD 93/42/EEC (and subsequent
changes) and its normatives.
IMPORTANT INFORMATION FOR CORRECT DISPOSAL OF THE PRODUCT IN ACCORDANCE WITH EC
DIRECTIVE 2012/19/UE-WEEE:
The symbol on the device indicates the separated collection of electric and electronic equipment. At the end of
life of the device, don’t dispose it as mixed solid municipal waste, but dispose it referring to a specific
collection centre located in your area or returning it to the distributor, when buying a new device of the
sample type to be used with the same functions. This procedure of separated collection of electric and
electronic devices is carried out forecasting a European environmental policy aiming at safeguarding,
protecting and improving environment quality, as well as avoiding potential effects on human health due to
the presence of hazardous substances in such equipment or to an improper use of the same or of parts of the
same
Caution:
The wrong disposal of electric and electronic equipment may involve sanctions.
