EGi GES 400 MR, Руководство пользователя

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GES 400 MR Series User Manual | 8100401-55 • 2015-07-22
1.4.7 Other Devices, System Accessories, and
Peripherals
WARNING:
• Evaluate leakage risk. If the GES is used in conjunction with
electric stimulation devices, ask qualified personnel to evaluate
any possible risk resulting from the sum of the leakage currents or
connections within the GES, in compliance with IEC 60601-1.
• GESs are not protected from defibrillation potentials. Do not
use GES components simultaneously with a defibrillator. If you
must use a defibrillator, disconnect the HC GSN from the
amplifier and move the amplifier away from the patient.
• Certify all accessory equipment according to the relevant IEC
standards.
Accessory equipment connected to the digital or
clock sync ports of the amplifier must be certified according to
the respective IEC standards (e.g., IEC 60950 for data processing
equipment and IEC 60601-1 for medical equipment).
Furthermore, all configurations shall comply with the system
standard IEC 60601-1-1. Any person who connects additional
equipment to the signal input port or signal output port
configures a medical system, and is therefore responsible for
ensuring that the system complies with the requirements of the
system standard IEC 60601-1-1. If in doubt, consult EGI Technical
Support (Table P-3).
• Use only accessories, cables, and replacement parts sold by
EGI.
The use of accessories and cables other than those that
ship with the GES, with the exception of those sold by EGI as
replacement parts for internal components, may result in
increased emissions or decreased immunity of the GES.
• Avoid stacking or adjoining EGI equipment with other
equipment.
EGI equipment should not be used adjacent to or
stacked with other equipment. If adjacent or stacked use is
necessary, EGI equipment should be observed to verify normal
operation in the configuration in which it will be used.