ERROR IDENTIFICATION
WARNING! If on the display TEMP.°C
(Pos. 9) appear the sign
it means
that the internal temperature probe sensor is out of order.
ORDINARY MAINTENANCE
Before initiating any maintenance operation, make sure that:
the device is not connected to the power source.
the device is at ambient temperature.
Keep the internal parts and the grid perfectly clean. Even though they may change colour and
become brownish, never use abrasive or inflammable products for cleaning them.
Keep the external parts perfectly clean that they have to be always specular to prevent corrosion and
dust.
PERIODIC MONTHLY MAINTENANCE
After removing the plug from the power socket, check that the fuses are not oxidised specially when
the device is not used for a long time or kept in a humid ambient.
The power socket should not change colour or oxidise. If that happens, replace it immediately.
The power cable must be integral and it should not show cuts, abrasions or bending.
The resistances and the internal electrical system do not require any maintenance.
PERMITTED USES
The device can be used to sterilize metal materials whose melting point is higher than 300°C
(surgical instruments, plates, and metal screw).
Inside the sterilizer place only metal containers without plastic parts and without textile material.
FORBIDDEN USES
It is forbidden to place in the device items whose melting temperature is lower than 300°C or is not
known to the operator.
ACCESSORY PARTS
2 Internal shelves
1 Mains cable
SELLING OFF
The sterilizing unit is made of various materials with mechanical, electro-mechanical and electronic
parts.
The selling off has to be made according with the regulations in force in the utilizing Nation.
***ATTENTION***
Laboratory tests following a cycle of 120 minutes at 180ºC on Bacillus subtilis var niger ATCC
9372 spores demonstrated the efficiency of the sterilizer.
Titanox does not guarantee and cannot ensure the effective achievement of the sterile state of the
instruments placed in the sterilizer, according to the definition of sterile medical instruments foreseen
by the EN 556 Norms. The user of the sterilizer therefore has the responsibility to conduct all of the
confirmation procedures of the sterilization process and the necessary verifications in order to ensure
the effective completion of every single sterilization cycle.
CPS CONTROL PANEL
9
2
(7)
CPS CONTROL PANEL based
on 8 bit microcontroller
