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1
Safety Notes
1.12 Maintenance
Page 16
Art
.
no.
:
2.
51
1335
Rev.
a
CARDIOVIT CS-104
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,
Содержание CARDIOVIT CS-104
Страница 1: ...User Guide CARDIOVIT CS 104 Art no 2 511335 Rev a 2 511335 ...
Страница 12: ...Page 12 Art no 2 511335 Rev a CARDIOVIT CS 104 ...
Страница 170: ...19 Annex Installation 19 5 Connection Overview Page 170 Art no 2 511335 Rev a CARDIOVIT CS 104 ...
Страница 172: ...Page 172 Art no 2 511335 Rev a 20 Index CARDIOVIT CS 104 ...