Smiths Medical 1818R, Руководство по эксплуатации и обслуживанию

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Chapter 1: Introduction
Oximeter Operation and Service Manual 1-5
Warnings, Cautions, and Notes
2
WARNING! Federal law (USA) restricts this device to sale
by, or on the order of, a physician.
2
WARNING! This device is not intended for continuous
patient monitoring. This device is intended to measure the
patient’s %SpO
2
and pulse rate values. There are no audi-
ble or visible alarms.
2
WARNING! This device must be used in conjunction with
clinical signs and symptoms. This device is only intended
to be an adjunct in patient assessment.
2
WARNING! Do not use this device in the presence of flam-
mable anesthetics.
2
WARNING! Do not use this device in the presence of mag-
netic resonance imaging (MR or MRI) equipment.
2
WARNING! Prolonged use or the patient’s condition may
require changing the sensor site periodically. Change sen-
sor site and check skin integrity, circulatory status, and
correct alignment at least every 4 hours.
2
WARNING! When connecting this monitor to any instru-
ment, verify proper operation before clinical use. Refer to
the instrument’s user manual for full instructions. Acces-
sory equipment connected to the monitor’s data interface
must be certified according to the respective IEC stan-
dards, i.e., IEC 950 for data processing equipment or IEC
601-1 for electromedical equipment. All combinations of
equipment must be in compliance with IEC 601-1-1 sys-
tems requirements. Anyone connecting additional equip-
ment to the signal input port or signal output port
configures a medical system, and, therefore, is responsi-
ble that the system complies with the requirements of the
system standard IEC 601-1-1.