Appendix 4: EMC Compatibility
Portable and Mobile RF communications equipment can affect the GSI Pello.
Install and operate the GSI Pello according to the EMC information presented on
this page and the next 4 pages.
The GSI Pello has been tested for EMC emissions and immunity as a standalone
instrument. Do not use the GSI Pello adjacent to or stacked with other electronic
equipment. If adjacent or stacked use is necessary, the user should verify normal
operation in the configuration.
The use of accessories, transducers and cables other than those specified, with the
exception of servicing parts sold by GSI as replacement parts for internal
components, may result in increased EMISSIONS or decreased IMMUNITY of
the device. Anyone connecting additional equipment is responsible for making
sure the system complies with the IEC 60601-1-2 standard.
Warning
•
This instrument is suitable in hospital environments except for near active HF
surgical equipment and RF shielded rooms of systems for magnetic resonance
imaging, where the intensity of electromagnetic disturbance is high
•
Use of this instrument adjacent to or stacked with other equipment should be avoided
because it could result in improper operation. If such use is necessary, this
instrument and the other equipment should be observed to verify that they are
operating normally
•
Use of accessories, transducers and cables other than those specified or provided by
the manufacturer of this equipment could result in increased electromagnetic
emissions or decreased electromagnetic immunity of this equipment and result in
improper operation. The list of accessories, transducers and cables can be found in
this appendix.
•
Portable RF communications equipment (including peripherals such as antenna
cables and external antennas) should be used no closer than 30 cm (12 inches) to any
part of this instrument, including cables specified by the manufacturer. Otherwise,
degradation of the performance of this equipment could result.
NOTICE
•
ESSENTIAL PERFORMANCE for this instrument is defined by the manufacturer
as:
This instrument does not have an ESSENTIAL PERFORMANCE Absence or loss of
ESSENTIAL PERFORMANCE cannot lead to any unacceptable immediate risk
•
Final diagnosis shall always be based on clinical knowledge There are no deviations
from the collateral standard and allowances uses
•
This instrument is in compliance with IEC60601-1-2:2014, emission class B group 1
NOTICE: There are no deviations from the collateral standard and allowances uses
NOTICE: All necessary instruction for maintaining compliance with regard to EMC can
be found in the general maintenance section in this instruction. No further steps required.