Huntleigh Healthcare Limited Huntleigh Diagnostic Products Division SF1US 사용자 설명서
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2.1 WARNINGS
The Sonicaid™ Freedom should only be used by personnel
familiar with the operation of electro-medical equipment,
especially for electronic monitoring of the fetal heart rate.
familiar with the operation of electro-medical equipment,
especially for electronic monitoring of the fetal heart rate.
A possible explosion hazard exists if used in the presence of
fl ammable anaesthetics.
fl ammable anaesthetics.
The Sonicaid™ Freedom should not be used at temperatures
lower than 10 or higher than 40 degrees centigrade.
lower than 10 or higher than 40 degrees centigrade.
Do not mount the unit directly above the patient. Locate the
unit so that it will not cause harm should it fall.
unit so that it will not cause harm should it fall.
Do not operate the unit from the mains supply if the mains
cable is damaged.
cable is damaged.
Do not immerse any portion of the receiver unit in water or
other liquids. The transducers are watertight and may be used
in water (IPX8 - TRANSDUCERS ONLY).
other liquids. The transducers are watertight and may be used
in water (IPX8 - TRANSDUCERS ONLY).
If there is any damage to the transducer housings, do not use
the transducer under water. Refer the transducer to Huntleigh
Healthcare qualifi ed service personnel for repair.
the transducer under water. Refer the transducer to Huntleigh
Healthcare qualifi ed service personnel for repair.
The transducers are protected from damage if dropped. Never
use the transducer without its protective sleeve. It can be
removed for cleaning in accordance with the Cleaning and
Disinfection Procedure in Section 6.
use the transducer without its protective sleeve. It can be
removed for cleaning in accordance with the Cleaning and
Disinfection Procedure in Section 6.
If this product is connected to another item of electrical
equipment, it is important that the system is fully compliant
with IEC60601-1.
equipment, it is important that the system is fully compliant
with IEC60601-1.
The device is generating RF-radiation. It is designed for use in
hospitals and other clinical settings, also outside of shielded
areas. As in other medical electrical devices, fi xed and mobile
RF-communication devices may disrupt the performance of the
Sonicaid™ Freedom.
hospitals and other clinical settings, also outside of shielded
areas. As in other medical electrical devices, fi xed and mobile
RF-communication devices may disrupt the performance of the
Sonicaid™ Freedom.
The telemetry equipment is classifi ed as IIb according to
Medical Devices Directive 93/42/EEC. The receiver unit is
connected to the AC line without a protective earth (Class 2).
The line voltage may be between 100 and 240V with 50 to 60Hz.
The transducer units are powered by safe current limited low
voltage re-chargeable batteries of 3.7V. Transducers are Class
CF.
Medical Devices Directive 93/42/EEC. The receiver unit is
connected to the AC line without a protective earth (Class 2).
The line voltage may be between 100 and 240V with 50 to 60Hz.
The transducer units are powered by safe current limited low
voltage re-chargeable batteries of 3.7V. Transducers are Class
CF.