1.
Check the condition of the unit before each use. The surface of the unit should carefully inspected for visual damage.
the mains cable and do not connect to power if damage is apperent;
2.
Before connecting the appliance always check that the electric data indicated on the data label and the type of plug used, correspond to those
of the mains electricity to witch it's to be connected;
3.
If the plug supplied with the appliance is incompatible with the mains electricity socket, contact qualified staff for replacement of the plug with
a suitable type. The use of simple or multiple and / or extension adapters is not generally recommended.
use is indispensable, use those in compliance with safety regulations, however paying attention not to exceed the maximum power supply
limits, which are indicated on the adapters and extensions;
4.
Respect the safety regulations indicated for electrical appliances and particularly:
•
Use original components and accessories provided by the manufacturer to guarantee the highest efficiency and safety of the device;
•
The device can be used only with the bacteriological filter;
•
Never immerge the appliance into water;
•
Place instrument on stable and flat surfaces;
•
Position the device in a way that the air inlets on the back aren't obstructed;
•
Don't use in the presence of inflammable substances such as anaesthetic, oxygen or nitrous oxide;
•
Don't touch the device with wet hands and always prevent the appliance coming into contact with liquids;
•
Keep off the reach of children or not capable people without supervision;
•
Don't leave the appliance connected to the power supply socket when not in use;
•
Don't pull the power supply cable to disconnect the plug remove the plug from the mains socket correctly;
•
Preserve and use the medical device in environments protected from atmospheric factors and at a distance from heat sources;
•
Don't use the device thoracic drainage.
5.
For repairs, exclusively contact technical service and request the use of original spare parts.
Failure to comply with the above can jeopardise the safety of the device;
6.
This medical device must be destined exclusively for the use for witch it has been designed ad described in this manual.
Any different use must be considered incorrect and therefore dangerous; the manufacturer will not be responsible for damage due to improper
use or connection to an electrical system not complying with current regulations;
7.
Particular precautions must be made concerning electromagnetic compatibility. The medical device must be installed and used according to
information supplied with the accompanying documents;
8.
Instrument and accessories discharging must be done following current law regulations in every country of use.
9.
None of electric or mechanical parts have been designed to be repaired by customers or end-users. Don't open the device, do not mishandle
the electric / mechanical parts. Always contact technical assistance
10. 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.
IMPORTANT INFORMATION FOR CORRECT DISPOSAL OF THE PRODUCT IN ACCORDANCE WITH EC DIRECTIVE 2002/96/EC:
In respect of art. 13 Decreto Legislativo 25 Luglio 2005, n.151 "Actuation of European directives 2002/95/EC, 2002/96/EC and 2003/108/EC, for reduction in
The symbol as over applied on the device or its packaging means that at the end of its useful life the product must not be disposed of with domestic waste.
At the end of device useful, the user will must deliver it to the able collecting centres for electric and electronic garbage, or give back to the retailer in the
moment of equivalent new device purchasing, one against one. Disposing of the product separately prevents possible negative consequences for the
environment and for health, deriving from inadequate disposal. It also allows the recovery of materials of witch it's made up in order to obtain an important
saving of energy and resources and to avoid negative effects to the ambient and health. In case of abusive disposal of device by user, will be applied
TYPOLOGY (MDD 93/42/EEC)
MODEL
CLASSIFICATION UNI EN ISO 10079-1
MAIN VOLTAGE
POWER CONSUMPTION
FUSE
MAXIMUM SUCTION PRESSURE (without jar)
MINIMUM SUCTION PRESSURE (without jar)
MAXIMUM SUCTION FLOW (without jar)
WEIGHT
SIZE
DUTY CYCLE (to 35°C and 110% operating voltage)
SICILICONE TUBE SIZE
ACCURANCY OF VACUUM INDICATOR
WORKING CONDITION
CONSERVATION CONDITION AND TRASPORT
use of dangerous substances in the electric and electronic device and for garbage disposal"
administrative endorsements in compliance with current standard.
TECHNICAL CHARACTERISTICS
Dispositivo Medico Classe IIa
Electric suction pump
HIGH VACUUM / HIGH FLOW
-80kPa (-0.80 Bar)
Less -40kPa (-0.40 Bar)
350 x 210 (h) x 180 mm
NON-STOP OPERATED
Room temperature:
Room humidity percentage:
Altitude:
Room temperature:
8
230V~ / 50Hz
107 VA
F 1 x 1.6A 250V
40 l/min
3.6 Kg
Ø 6 x 10 mm
± 5%
5 ÷ 35°C
30 ÷ 75% RH
0 ÷ 2000m s.l.m.
-40÷ 70°C
Check
Whenever their