Product Manual
Oximeter SerieSOximeter SerieS
PULSE OXIMETER INSTRUCTION MANUAL
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hazard may exist. All servicing and future upgrades must
be carried out by trained personnel and authorized by
our company only.
• The Pulse Oximeter is specied for use by medical
professionals only.
• Prolonged use of the probe/sensor or the patient’s condition
may require changing the sensor site periodically. Change
the sensor site and check skin integrity, circulatory status,
and correct alignment at least every 4 hours. Prolonged use
may cause blisters, skin deterioration, and discomfort.
• When connecting this Oximeter to any instrument,
verify proper operation before clinical use. Refer to
the instrument’s user manual for full instructions. The
equipment connected to the Pulse Oximeter’s data
interface must be certied according to the respective
IEC standards, i.e., IEC950 for data processing equipment
or IEC 601-1 for medical electrical equipment. All
combinations of equipment must be in compliance with
IEC601-1-1 systems requirements.
• Sensor malfunction may cause inaccurate data, possibly
resulting in patient injury or death, so pay close
attention to the sensor and inspect it often.
• The physiological data and alarm messages displayed
on the equipment are for reference only and cannot be
directly used for diagnostic interpretation.
• Do not rely exclusively on the audible alarm system
for patient monitoring. Adjustment of alarm volume
to o may result in a hazard to the patient. Remember
that alarm settings should be customized according