Mindray DC-40 Operator's Manual page 20

Diagnostic ultrasound system
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1-4 Safety Precautions
9.
DO NOT use a probe that has a damaged, scratched surface, or
exposed wiring of any kind. Immediately stop using the probe
and contact Mindray Customer Service Department or sales
representative. There is risk of electric shock if using a
damaged or scratched probe.
10. Do not allow the patient to contact the live parts of the
ultrasound system or other devices, e.g. signal I / O ports.
Electric shock may occur.
11. Do not use an aftermarket probe other than those specified by
Mindray. The probes may damage the system causing a
profound failure, e.g. a fire in the worst case.
12. Do not subject the probes to knocks or drops. Use of a
defective probe may cause an electric shock.
13. Do not open the covers and front panel of the system. Short
circuit or electric shock may result when the system hardware
is exposed and powered on.
14. Do not use this system when any digital device such as a high-
frequency electrotome, high-frequency therapeutic device or
defibrillator is applied already. Otherwise, there is a risk of
electric shock to the patient.
15. Only use the ECG leads and PCG transducer provided with the
physiology module; otherwise, electric shock may be resulted.
16. When moving the system, you should hold the handle;
otherwise, damage may be resulted by abnormal force. Do not
push the system from the left/right side; otherwise, it may be
toppled over.
17. The auxiliary power output outlet in the system is used to
supply power for the recommended peripheral devices. Do not
connect other devices to the outlet, otherwise, the rated output
power may be exceeded and failure may be resulted. Maximum
output power of the outlet is 240VA (including the auxiliary
output port in the printer compartment).
18. Accessory equipment (analog or digital) connected to the
ultrasound system must comply with the relevant IEC
standards (e.g., IEC 60950 information technology equipment
safety standard and IEC 60601-1 medical equipment
standard).Furthermore, all configurations must comply with the
standard IEC 60601-1-1.It is the responsibility of the person,
who connects additional equipment to the signal input or
output ports and configures a medical system, to verify that the
system complies with the requirements of IEC 60601-1-1.If you
have any questions regarding these requirements, consult your
sales representative.
19. Prolonged and repeated use of keyboards may result in hand or
arm nerve disorders for some individuals. Observe the local
safety or health regulations concerning the use of keyboards.
20. When using intra-cavity probes, do not activate the probe
outside the patient's body.

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