CARESCAPE Monitor B850
52
2106778-001
(isolating or separating transformer). Using without an isolating
transformer could result in unacceptable enclosure leakage currents.
Environmental requirements
•
Install the patient monitor to a location that meets the specified environmental
requirements of operating temperature, humidity and atmospheric pressure.
•
Set up the device in a location which affords sufficient ventilation. The ventilation
openings of the device must not be obstructed.
EMI & RFI interference:
WARNING
Do not use the monitor in high electromagnetic fields (for example,
during magnetic resonance imaging).
CAUTION
EMC - Magnetic and electrical fields are capable of interfering with the proper
performance of the device. For this reason make sure that all external devices
operated in the vicinity of the monitor comply with the relevant EMC
requirements. X-ray equipment or MRI devices are a possible source of
interference as they may emit higher levels of electromagnetic radiation.
Changes or modifications to this device/system not expressly approved by GE
may cause EMC issues with this or other equipment. This device/system is
designed and tested to comply with applicable standards and regulations
regarding EMC and needs to be installed and put into service according to the
EMC information stated as follows: This device/system is suitable for use in all
establishments other than domestic and those directly connected to the public
low-voltage power supply network that supplies buildings used for domestic
purposes. Mains power should be that of a typical commercial or hospital
environment. Device is compliant to Class A.
CAUTION
Use of known RF sources, such as cell/portable phones, or other radio
frequency (RF) emitting equipment near the system may cause unexpected or
adverse operation of this device/system. Consult qualified personnel regarding
device/system configuration.
•
The patient monitor should be isolated from sources of strong electromagnetic and radio
frequency interference.
NOTE: Refer to the patient monitor’s supplemental information manual for more information.
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