Electromagnetic Compatibility - Cardinal Health Alaris 8000 Series Directions For Use Manual

Modular system intended for adult, pediatric and neonatal care in today’s growing professional healthcare environment
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Electromagnetic Compatibility

WARNINGS
• Do not use the Alaris
Imaging (
).
MRI
• Use of any accessory, transducer or cable other than
those specified may result in increased emissions or
decreased Alaris
®
CAUTIONS
• The Alaris
System should not be used adjacent to or
®
stacked with other equipment. If adjacent or stacked use
is necessary, monitor the Alaris
operating normally in that setup.
• The Alaris
System is intended for use by healthcare
®
professionals only. This is a
medical system. In a domestic environment, this system
may cause radio interference. Reorienting, relocating or
shielding the system, or filtering the connection to the
public mains network, are examples of steps that can be
taken to reduce or eliminate interference.
• Medical electrical equipment needs special precautions
regarding
and needs to be installed and used
EMC
according to the
EMC
"Appendix" Section of this
Standards", "Compliance").
• Portable and mobile
medical electrical equipment.
• Interconnected data communications systems must be
certified to
IEC 950
(electromedical equipment).
IEC 60601–1
• Nurse call systems must be certified to
signaling and nurse call equipment) or comply with the
requirements specified in
1-24
General Information
Warnings and Cautions (Continued)
System near Magnetic Resonance
®
System immunity.
System to verify it is
®
CISPR 11
information provided in the
(reference "Regulations and
DFU
communications can affect
RF
(data processing equipment) or
.
IEC 60601–1
Class
Group
B
2
(hospital
UL 1069
Alaris
System Directions for Use
®
PC Unit Section

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