Sleep&Go
User’s Manual
534-7AB-MU2 • REV. 1.07
User
’s Manual -
Cardior
espiratory polygraph
- Sleep&Go
28
not quantify the degree of existing hyperoxemia.
•
Interferences such as movements, abnormal hemoglobins,
intravascular contrasts, states of low perfusion and skin
pigmentation may affect the operation of the pulse oximeter.
• It is unlikely that organisms are transmitted via pulse oximetry.
However, we recommend washing the pulse oximetry sensor for
each change of patient with soapy water or disinfectant solution
as specified by the manufacturer.
•
The pulse oximetry module and the pulse oximetry probe is CE
marked. The temperature of the area of the probe in contact
with the finger will not reach temperatures > 42 °.
•
See the instructions for use before use. Strictly follow the
manufacturer’s safety instructions, as well as those specified
in this manual.
•
The maximum recommended time of application of an pulse
oximeter in the same place is 24 hours. The point of placement
must be checked frequently to determine the position, circulation
and cutaneous sensitivity of the patient. Reaction to the sensors
by the patients may be different depending on their state of
health and skin condition. Adhesive material must not be used
if the patient shows an allergic reaction to such material.
• For long-term measurements, it is recommended to use flexible
or disposable sensors.
• The adult sensor is for people over 12 years of age (>40 kg).
The pediatric sensor is for children aged between 5 and 12
years of age (15-40 kg).
•
The system can measure the pulse rate and functional oxygen
saturation. A functional meter can not be used to evaluate the
accuracy of a pulse oximetry sensor or a pulse oximetry monitor.
• Do not use blood flow restrictors because they can lead to loss
of signal.
