The physician defines the protocol and ensures that it is correctly implemented (adjustments, session duration and
frequency of use).
The first cycle of the movement need to be done without the patient.
The patient must know the start/stop/reverse function on the control handle. Hand control must be accessible to patient at
all times. (See page 7).
KINETEC C.E.M. complies with Directive 93/42/CEE.
KINETEC C.E.M. is not designed for use in the presence of flammable anesthetics.
In case of electromagnetic interference with other devices move the device.
KINETEC C.E.M. is in compliance with standards in force (IEC 601.1.2), electromagnetic compatibility standard for medical devices.
Please, do not touch the moving parts while the unit is running, pinching risk.
KINETEC C.E.M is a type B class I device.
Before connecting the device to the power supply, check that the mains
voltage matches that shown on the identification plate (100-240 V~ 50-
60Hz).
Connect the hand control and motors.
The cables (motor and hand control) can be plugged in any of the
connectors
Connect the power supply cable (25).
IMPORTANT
Check that the electrical socket is in good condition and is
suitable for the splint power supply cord. The latter complies with
current standards and has a grounding socket.
The plug may be connected to any standard socket.
The socket must however have a grounded pin.
To connect the power supply, only use the original cable supplied
with the machine.
Check that the cables remain free around the device so that they
do not get damaged.
Switch on (26). The light (27) is ON
While the unit begins an auto diagnostic, the display shows the following
KINETEC
ELBOW MODULE 1.0
Your KINETEC C.E.M. is ready to be used.
Comment: The values of the movements are record when the machine is switched on/off (except Timer and Warm
Up mode).
EXPLOSION HAZARD:
Please wait
Electrical Connection
26
25
27
ELBOW MODULE
0
STOP
Safety
Starting the unit
80
135
GB
5