CA.MI Clineb Pro Gebrauchsanweisung - Seite 3

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EN
13.
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;
14.
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.
15.
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.
Model
Typology (MDD 93/42/EEC)
Power Feeding
Power Consumption
Fuse
Max Pressure
Max Air Flow
Operating Pressure
Operating Air Flow
NEBULIZZAZIONE (**)
MMAD (µm) *
Mass Median Aerodynamic Diameter
GSD (*)
Geometric Standard Deviation
Output Rate (ml/min) *
Output (ml) *
Weight
Size
Noise Level (measured as specifications of EN 13544-1)
Duty Cycle
Min Capacity Nebulizer
Max Capacity Nebulizer
Working Condition
Conservation condition and Transport
(*) Data determined with Cascade Impactor 290 series, compliant with EN 13544-1, by spraying 2 ml of NaF 1.0%.
(**) Data from free nebulisation of 2 ml of NaCl 0.9% (average nebulisation value per minute).
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.

TECHNICAL CHARACTERISTICS

Pos. A
(closed)
0,40 ml
Pos. A
(closed)
Pos. A
(closed)
Pos. A
(chiuso)
0.077
Pos. A
(closed)
0.189
Room temperature:
Room humidity percentage:
Atmospheric pressure:
Room temperature:
Room humidity percentage:
Atmospheric pressure:
3
CLINEB PRO
Class IIa Medical device
230V ~ / 50 Hz
170VA
F 1 x 1.6A L 250V
300 kPa (3.0 Bar)
16 l/min
95 kPa (0.95 Bar)
8.0 l/min a 95kPa
Pos. B
0,60 ml
Pos. B
3.32
4.07
Pos. B
4.12
2.64
Pos. B
0.105
Pos. B
0.237
2.20 Kg
230 x 250 (H) x 190mm
Approx. 60dB (A)
Non-Stop Operated
2ml
8ml
Pos. C
Pos. D
0,70 ml
0,80 ml
Pos. C
Pos. D
4.23
4.18
Pos. C
Pos. D
2.74
2.49
Pos. C
Pos. D
0.124
0.138
Pos. C
Pos. D
0.247
0.260
5 ÷ 40 °C
10 ÷ 93 % RH
700 ÷ 1060 hPa
- 25 ÷70 °C
0 ÷ 93% RH
500 ÷ 1060 hPa