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Samsung MYSONO U6 Manual de usuario Pagina 25

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1-7
Chapter 1 Safety
Electrical Safety
This equipment has been veried as a Class I device with Type BF applied parts.
Prevention of Electric Shock
WARNING:
X
Electric shock may result if this system, including all of its externally mounted recording and
monitoring devices, is not properly grounded.
X
Never remove the cover from the product. This product uses levels of voltage that are
potentially dangerous. All internal component repairs and part replacements must be
performed by Samsung Medison’s service department.
X
Always check the product’s casing, cables, cords, and plugs for damage before using the
product. Do not use and disconnect the power source, if the face is cracked, chipped, or torn,
the housing is damaged, or if the cable is worn.
X
Always disconnect the system from the wall outlet prior to cleaning the system.
X
All patient contact devices, such as the probe, must be detached from the patient prior to using
a high-voltage defibrillator.
X
The use of flammable anesthetic gas or oxidizing gases should be avoided. Doing so may cause
an explosion.
X
Avoid installing the system in such a way that it is difficult for the operator to disconnect it from
the power source.
X
Only use an AC adapter recommended by Samsung Medison.
X
Do not use together with HF surgical equipment. HF surgical equipment may be damaged,
which may result in fire.
X
The System must only be connected to a supply mains with protective earth to avoid risk of
electric shock.
CAUTION:
X
An isolation transformer protects the system from power surges. The isolation transformer
continues to operate when the system is in standby.
X
Do not immerse the cable in liquids. The power cable is not waterproof.
X
Do not touch the SIP/SOP terminal on the rear of the product while diagnosing the patient.
There is a risk of electric shock from leakage current.
Additional equipment connected to medical electrical equipment must comply with the respective IEC
standards (e.g. IEC 60950/EN60950 for data processing equipment, IEC60601-1/EN60601-1 for medical
devices). Furthermore, all congurations shall comply with the requirements for medical electrical
systems (see IEC60601-1-1/EN60601-1-1). Anybody connecting additional equipment to signal input
and output port of medical electrical equipment should make sure that the equipment complies with
IEC60601-1-1/EN60601-1-1.
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