Maintenance; Operation With Other Devices - Schiller CARDIOVIT CS-104 User Manual

1 Safety Notes

1.12 Maintenance

Page 16
1.12 Maintenance
 No serviceable parts inside the CARDIOVIT CS-104 nor the ECG Recorders or
SpiroScout. Refer servicing to a qualified technician authorised by SCHILLER
only.
 Do not use high temperature sterilisation processes (such as autoclaving). Do not
use E-beam or gamma radiation sterilization.
 Do not use solvent or abrasive cleaners on either the unit or cable assemblies.
 Do not under any circumstances, immerse an ECG recorder, SpiroScout, or any
cable assembly in liquid.
1.13

Operation with other Devices

 Accessory equipment connected must be certified according to the respective
IEC standards (e.g. IEC/EN 60950 for data processing equipment and IEC/EN
60601-1 for medical equipment). Furthermore, all configurations shall comply
with the valid version of IEC/EN 60601-1. Everybody who connects additional
equipment to the signal input part or signal output part configures a medical
system and is therefore responsible that the system complies with the
requirements of the valid version of IEC/EN 60601-1. If in doubt, contact the
technical service department or your local representative.
 Any other equipment used with the patient must use the same common earth as
the CARDIOVIT CS-104.
 Special care must be exercised when the unit is used with high-frequency
equipment. Use the special high-frequency SCHILLER patient cable to avoid
possible signal interference during ECG acquisition. However, the stimulation
units should only be used at a sufficient distance from the electrodes and both
devices must be connected to the same potential equalisation. If in doubt, the
patient should be disconnected from the device.
 This device can safely be used with pacemaker patients.
 There is no danger when using this device simultaneously with electrical
stimulation equipment.
 If the device is part of a medical system, only the original SCHILLER patient cable
must be used with, and connected to, the CARDIOVIT CS-104.
 If the patient cable should become defective after defibrillation, a lead-off
indication is displayed on the screen.
 Portable communication devices, HF radios and devices labelled with the
symbol (non-ionic electromagnetic radiation) can affect the operation of this
device (see para. 18.10, Measures to Prevent Electromagnetic Interferences,
page 163).
CARDIOVIT CS-104