9
TECHNICAL CHARACTERISTICS
TYPOLOGY (MDD 93/42/EEC)
Class IIa Medical Device
MODEL
SUPER VEGA BATTERIA
UNI EN ISO 10079-1
HIGH VACUUM / LOW FLOW
POWER FEEDING
230V~ / 50Hz or Internally powered equipment
(PB Battery 12V 3Ah) or 12Vdc (1.9A) from car battery
POWER CONSUMPTION
50VA
FUSE
F 1 x 630mA 250V
MAXIMUM SUCTION PRESSURE (without jar)
-75kPa (-0.75 Bar)
MINIMUM SUCTION PRESSURE (without jar)
Less – 40kPa (-0.40 bar)
MAXIMUM SUCTION FLOW (without jar)
16 l/min
WEIGHT
4.9 Kg
SIZE
350 x 210 x 180mm
BATTERY HOLDING TIME
45 ÷ 50 minutes
BATTERY TIME CHARGE
120 ÷ 150 minutes
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
SYMBOLS
Class II isolation equipment
CE marking in conformity with EC directive 93/42/EEC
Manuafcturer: CA.MI. di Attolini Mario & C. snc
Via Ugo La Malfa nr.31 – 43010 Pilastro (PR) Italy
Warning, consult the instruction manual
To Preserve in place coolness and dry land
Conservation temperature: -40 ÷ 70°C
Type B equipment
Fuse
~
Alternate Current
Battery
Direct Current
Hz
Mains Frequency
I
ON
O
OFF
ACCESSORIES SUPPLIED
DESCRIPTION
COMPLETE ASPIRATION JAR 1000cc
CONICAL FITTING
TUBES SET 6 mm x 10 mm
ASPIRATION PROBE CH20
ANTIBACTERIAL FILTER
The filter is produced with (PTFE) hydrophobic material witch prevents fluids entering the pneumatic circuit. When the filter is wet, it’s not possible to use
the unit therefore the filter should be changed immediately. In case of possible contamination or discolouration, change the filter immediately.
Don’t use the suction unit without the protection filter fitted. If the suction unit is used in an emergency or in a patient where the risk of contamination is not
know the filter must be changed after each use. Available under request with different versions with complete jar 2000cc.
The suction probe must be changed at the end of each application.
WARNING: Suction tubes for insertion in the human body purchased separately from the machine should comply with ISO 10993-1 standards
on material biocompatibility.
