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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.
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.
11.
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.
12.
The medical device is in contact with the patient by means of a disposable probe (supplied with the device) furnished with
the relative CE compliance certification according to the requirements of regulation ISO 10993-1: thus, no allergic reactions
and skin irritations may occur.
13.
The product and its parts are biocompatible in accordance with the requirements of regulation EN 60601-1.
14.
Operation of the device is very simple and therefore no further explanations are required other than those indicated in the
following user manual.
The lead 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.
The manufacturer 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
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.
Model
Typology (MDD 93/42/EEC)
Classification UNI EN ISO 10079-1
Main Voltage
Power consuption
Fuse
Maximum suction aspiration (without jar)
Minimum suction aspiration (without jar)
Maximum Suction Flow (without jar)
Weight
Insulation Class (when used with the power cable or with a
car cigarette lighter cable)
Insulation Class (when used with an Internal battery)
Size
Functioning
Battery Holding Time
Battery Time Charge
Accurancy of Vacuum Indicator
Working condition
Conservation and transport condition
normatives.
TECHNICAL CHARACTERISTICS
(Pb Battery 12V
Room temperature:
Room humidity percentage:
Atmospheric pressure:
Room temperature:
Room humidity percentage:
Atmospheric pressure:
16
AS-12V BR
Class IIa Medical device
HIGH VACUUM / LOW FLOW
230V~ / 50Hz or Internally powered equipment
2.8A) or with cigarette lighter adapter
(12V
50VA
1 x F 630mA L 250V
-75kPa (-0.75 bar)
Less -25kPa (-0.25 bar)
16 l /min
4.9 Kg
Class II
Internally Powered Equipment
357 x 193 x 215mm
Non-Stop Operation
45 ÷ 50 minutes
120 ÷ 150 minutes
± 5%
GB
1.9A)
5 ÷ 35 °C
10 ÷93 % RH
700 ÷ 1060 hPa
- 25 ÷70 °C
0 ÷ 93% RH
500 ÷ 1060 hPa
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