Huntleigh Sonicaid FM800 Series, Инструкция по эксплуатации, Страница: 9 / 130

Sonicaid FM800 Encore Series Instructions for Use
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Limitations for use
Fetal monitors provide just one indicator of fetal condition. This should be assessed as
part of an holistic approach to obstetric care together with other factors. A complete
assessment must be made before taking appropriate action.
FM800E series monitors are intended to show trends in fetal and maternal life signs to
give a “first line” indication. On-screen displays and printouts should not be used as a
basis for clinical diagnosis; always confirm vital sign parameters by other means before
making treatment decisions.
Ultrasound monitoring should be performed in accordance with current guidelines. The
ALARA guideline (AIUM) recommends that ultrasound exposure should be kept As Low
As Reasonably Achievable.
Do not use the maternal oximetry sensors during magnetic
resonance imaging (MRI) scanning. Induced current could
cause burns. The oximeter may affect the MRI image, and
the MRI unit may affect the accuracy of oximetry
measurements.
FM800E series monitors are not intended to be used in
conjunction with defibrillator equipment. All transducers
should be removed from the patient prior to using a
defibrillator to avoid possible equipment damage and/or
injury.
FM800E series monitors are not intended for use with
patients fitted with cardiac pacemakers.
FM800E series monitors are not intended for use in water
birth situations. Exposing the unit to water could give rise to
risk of electric shock.
FM800E series monitors are not intended for use in surgical
situations. Disconnect the unit before commencing any
surgical procedures.
FM800E series monitors are not intended for mobile use in
vehicles or in aircraft.
FM800E series monitors are not to be used by untrained
personnel. Users should be alert to the possibility that
machine settings or transducers may be tampered with when
the machine is left unattended.