CADENCE II Fetal Monitor User Manual
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IUP
This symbol indicates that this is an IEC/EN 60601-1 Type BF applied part.
DECG
This symbol indicates that this is an IEC/EN 60601-1 Type CF applied part.
A The monitor described in this user manual is not protected against:
a) The effects of defibrillator shocks
b) The effects of defibrillator discharge
c) The effects of high frequency currents
d) The interference of electrosurgery equipment
1.3 Ultrasound Safety Guide
A Fetal Use
The CADENCE II Fetal Monitor is designed for continuous fetal heart rate monitoring during
pregnancy and labor. Clinical interpretation of fetal heart rate trends can diagnose fetal and/or
maternal problems and complications.
A Instructions for Use in Minimizing Patient Exposure
The acoustic output of CADENCE II is internally controlled and can not be varied by the
operator in the course of the examination. The duration of exposure is, however, fully under the
control of the operator. Mastery of the examination techniques described in the User Manual will
facilitate obtaining the maximum amount of diagnostic information with the minimum amount of
exposure. The exercising of clinical judgment in the monitoring of low risk patients will avoid
unnecessary insonation.
1.4 Safety Precautions
To avoid the possibility of injury, observe the following WARNING and CAUTION messages
during the operation of the instrument.
WARNING :
For using safety:
A CADENCE II is provided for the use of qualified physicians or personnel
professionally trained. They should be familiar with the contents of this user manual
before operation.
A Only qualified service engineers can install this equipment. Only service engineers
authorized by the manufacturer can open the case.
A This device is not intended for home use.
A EXPLOSION HAZARD - Do not use the monitor in the presence of flammable
anesthetics or other materials.
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