Operation Manual

www.medicalsuction.co.uk
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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 use of dangerous substances in the electric and electronic device and
for garbage disposal”
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 administrative endorsements in compliance
with current standard.
TECHNICAL CHARACTERISTICS
TYPOLOGY (MDD 93/42/EEC) Dispositivo Medico Classe IIa
MODEL NEW ASPIRET
CLASSIFICATION UNI EN ISO 10079-1 HIGH VACUUM / LOW FLOW
MAIN VOLTAGE 230V~ / 50Hz
POWER CONSUMPTION 184VA
FUSE F 1 x 1.6A 250V
MAXIMUM SUCTION PRESSURE (without jar) -75kPa (-0.75 Bar)
from -75kPa (-0.75bar) to -10kPa (-0.10 bar)
MAXIMUM SUCTION FLOW (without jar) 15 l/min
WEIGHT 2.2 Kg
SIZE 250 x 190 (h) x 160 mm
DUTY CYCLE (to 35°C and 110% operating voltage) NON-STOP OPERATED
SICILICONE TUBE SIZE Ø 6 x 10 mm
ACCURANCY OF VACUUM INDICATOR ± 5%
WORKING CONDITION Room temperature: 5 ÷ 35°C
Room humidity percentage: 30 ÷ 75% RH
Altitude: 0 ÷ 2000m s.l.m.
CONSERVATION CONDITION AND TRASPORT Room temperature: -40÷ 70°C
Room humidity percentage: 10 ÷ 100% RH