C.B.M. S.r.l. Medical Equipment - Via Castello 10, 26038 Torre d
é
Picenardi (CR) - Italy
Rev. 7
–
24/07/2006
IGEA
Pag. 10 di 45
INDEX
Components legend ...................................page 10
Warnings ....................................................page 10
General information....................................page 11
Installation ..................................................page 12
User
’
s instructions ......................................page 12
Utility functions ...........................................page 13
RESET and COUNTER keys
(cycle interruption)
...................................page 13
Cleaning .....................................................page 13
Routine maintenance .................................page 13
First intervention guide ...............................page 14
Guarantee ..................................................page 15
WEEE.........................................................page 15
Sterilizing and drying times.........................page 15
Alarms Table ........................................... page 37-38
Safety table................................................ page 39
Wiring and hydraulic diagram.................. page 40-42
Technical particulars ..................................page 44
Declaration of conformity............................page 45
COMPONENTS LEGEND:
A)
Handwheel
B)
Reservoir lid
C)
Drain tap door
D)
Safety lever
E)
Feet nut
F)
Clutch to unload
G)
Main Switch with fuses
H)
Display
I)
Power
green led
J)
Door locked
green led
K)
Heating
yellow led
L)
Cycle
yellow led
M)
START -
and
ENTER
key
N)
CYCLE
and
RESET
key
O)
DRYING
and
COUNTER
key
P)
UTILITY
key
Q)
SHIFT
key
R)
EMPTY
red led
S)
OK
green led
T)
FULL
yellow led
U)
Manometer
V)
Green Main switch
W)
Serial outlet
X)
----------------
Y)
Reset key
WARNINGS
•
The use of this device is limited to qualified staff.
•
The sterilizer must be used only with distilled
water
•
Before using the equipment for the first time, we
recommend to check the cleaning of the sterilizing
chamber and to effect a loadless sterilizing cycle.
•
In case of power failure during the autoclave
sterilizing phase when the power comes back the
writing ALARM 12 - BLACK OUT appears on the
display, the cycle is considered invalid.
Anyway and in any case each cycle is to be
considered valid if at the end of the cycle the writing
OK - FINISHED CYCLE appears on the display.
•
In case of several running cycles the equipment
can reach high external temperatures.
•
In order not to contaminate the reservoir water,
we recommend you not to let any object leaning
on the machine and to check that the reservoir
cap is closed.
•
We recommend to use the autoclave in a clean
area.
•
Check that the material can be sterilized with the
chosen sterilization cycle.
•
In all cases of malfunction empty the chamber
connecting the silicone pipe linked to the water
drain tap to a container Then open the tap and the
water will flow from the chamber into the
external container.
•
Before screwing out any part of the sterilizer make
sure that this one is disconnected from the
feeding network.
•
This
equipment
has
been
designed
and
manufactured in compliance with the Comunity
regulation 93/42 EEC
"Medical devices"
and
C.B.M. S.r.l. is considered responsible concerning
safety, reliability and performances on condition
that possible modifications or repairs shall be
effected by personnel authorized by C.B.M. ,
provided that the environment electric equipment
is in compliance with IEC regulations and
provided that the equipment is used according to
these user
’
s instructions.
IMPORTANT
:
The
manufacturer
company
is
relieved of any responsibility for possible damages to
