Safety
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 5).
KINETEC Breva complies with Directive 93/42/CEE.
KINETEC Breva is not designed for use in the presence of flammable anesthetics.
In case of electromagnetic interference with other devices move the device.
KINETEC Breva is in compliance with standards in force (IEC 60601-1-2:2001), electromagnetic compatibility
standard for medical devices.
Please, do not touch the moving parts while the unit is running, pinching risk.
Electrical Connection
KINETEC Breva 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 (13) and the motor (12).
Connect the power supply cable (30).
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.
Starting the unit
Switch on (11).
While the unit begins an auto diagnostic, the display shows the following
Breva V01.0
Your KINETEC Breva 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).
GB
4
KINETEC
EXPLOSION HAZARD:
PL/flex dor/flex
Please wait
13
30
11
PL/flex dor/flex
20
STOP
12
0
20