Ca-Mi New Askir 118 Basic Manual De Instrucciones página 16

GB
9. 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.
10. The medical device is in contact with the patient by means of a disposable probe (supplied with the device). Suction tubes
for insertion in the human body purchased separately from the machine should comply with ISO 10993-1 standards on
material biocompatibility.
11. The product and its parts are biocompatible in accordance with the requirements of regulation EN 60601-1.
12. Operation of the device is very simple and therefore no further explanations are required other than those indicated in the
following user manual.
13. The battery integrated in the device is not to be considered as an ordinary domestic waste. Such a component must be
disposed of in a specific collection centre in order to be recycled.
14. Use in Home-Care: Keep all accessories of the device out of reach of children under 36 months of age since they contain
small parts that may be swallowed.
15. Do not leave the device unattended in places accessible to children and/or persons not in full possession of mental faculties
as they may strangle themselves with the patient's tube and/or the power cable.
- Before using the NEW ASKIR 118 BASIC, consult the instructions for use: failure to read all the instructions in this
manual can be harmful for the patient.
- The device cannot be used to drain chest fluids;
- The device must not be used for suction of explosive, corrosive or easily flammable liquids.
- NEW ASKIR 118 BASIC is not suitable for MRI. Do not introduce the device in MRI environments.
IMPORTANT INFORMATION FOR CORRECT DISPOSAL OF THE PRODUCT IN ACCORDANCE WITH EC
DIRECTIVE 2012/19/UE-RAEE: 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 returring 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.
Model
Typology (MDD 93/42/EEC)
UNI EN ISO 10079-1 Classification
Power Feeding
Maximum Suction Pressure (adjustable)
Minimum Suction Pressure (adjustable)
Maximum Suction Flow
Weight
Insulation Class (when used with AC/DC power adaptor or
with cigarettes lighter adaptor)
Insulation Class (when used with an Internal battery)
Size
Battery Holding Time
Battery Time Charge
Working Condition
Conservation condition and Transport
Please note that if the device is used at an altitude higher than 2,500 m asl, the yield intended as suction flow may vary sensitively
due to the decrease in atmospheric
CONTRAINDICATIONS
TECHNICAL CHARACTERISTICS
pressure.
NEW ASKIR 118 BASIC
Class IIa Medical device
HIGH VACUUM / HIGH FLOW
14V 4A with AC/DC adapter mod. UE60-140429SPA1 of
FUHUA (input: 100-240V~ - 50/60Hz - 100VA) or Internally
5,2 A - 14,8 V
powered equipment (
battery
) or with cigarette lighter adapter (12V
-75kPa (- 0.75 bar)
-15kPa (-0.15 bar)
Internally Powered Equipment
350 x 150 x 190 mm
Room temperature:
Room humidity percentage:
Atmospheric pressure:
Room temperature (≤ 1 mounth): :
Room Temperature (≤ 3 mounth):
Room Temperature (≤ 1 year):
Room humidity percentage:
Atmospheric pressure:
16
by internal Li-Ion
36 l /min
2.50 Kg
Class II
70 minutes
360 minutes
5 ÷ 40°C
0 ÷ 85% RH
800 ÷ 1060 hPa
- 20°C ÷ 45°C
- 20°C ÷ 35°C
0°C ÷ 25°C
0 ÷ 85% RH
500 ÷ 1060 hPa
4A)