Features And Displays - CareFusion Alaris 8015 User Manual

Electromagnetic Compatibility (Continued)
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 System to verify that it is
operating normally in that setup.
• Portable and mobile RF communications can affect
medical electrical equipment.
• Interconnected data communications systems must be
certified to IEC 60950 (data processing equipment) or
IEC 60601–1 (electromedical equipment).
• The Alaris System is intended for use by healthcare
professionals only. This is a CISPR 11 Class B Group 1
medical system. In a domestic environment, this system
can 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 EMC and needs to be installed and used
according to the EMC information provided in the
"Appendix" section of this User Manual (see "Regulations
and Standards," "Compliance").
Features and Definitions
See the product-specific section of this User Manual that applies to the attached module(s) for features
and definitions specific to that module.
Feature
Clinician ID
Data Set
PC Unit Section
Alaris System User Manual – with v9.33 Model 8015
Warnings and Cautions (Continued)

Features and Displays

An optional alphanumeric 16-character clinician identifier that can be
entered and displayed.
Created using Editor Software authoring tool and then transferred to
PC unit. A Data Set reflects facility's best-practice guidelines for
administration and includes: Profile Drug Libraries, Clinical Advisories,
instrument configurations, and Channel Label Libraries.
Definition
Drug
IV
General Information
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