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Preface Before You Begin
Safety Cautions and Warnings
Terason t3000 / Echo Ultrasound System User Guide
17
To limit exposure to electromagnetic interference from nearby equipment that can degrade
image quality, you should operate the Terason Ultrasound System under EMI conditions
that minimize power supply transients, mechanical interactions, vibration, and thermal,
optical, and ionizing radiation.
Electrostatic Discharge (ESD)
ESD, or static shock, is caused by rapid discharge of electrical energy from one body to another.
ESD is common in conditions of low humidity, such as those resulting from heating or air
conditioning. To avoid damage to transducers, electronics or system, use anti-static spray on
carpets and linoleum, and anti-static mats.
The Terason Ultrasound System complies to a level of ± 2kV ESD. The latch for locking
the ultrasound transducer and the FireWire port is sensitive to ESD and should not be
touched when operating the system. In cases where an ESD shock discharges to one of
these points, the computer program may freeze or windows may open unexpectedly. In
these cases, the Terason software may require restarting, and you may have to close extra
windows. In extreme cases, the computer may require restarting. These events are not
dangerous to the patient or to the operator.
Liquids
The Terason transducer, electronics envelope, and computer are not protected from spilled
liquids. The transducer array is watertight up to the strain relief, as specified in
on page 284. If the computer is exposed to liquids or moisture, purchase a
keyboard drape. In addition, the Terason Ultrasound System electronics must be draped if
exposed to liquids or moisture.
Couplants
Use only couplants specifically designed for ultrasound examinations. Do not use mineral-
oil or vegetable-based couplants, which can damage transducers.
Heat
Do not expose transducers to direct heat such as strong sunlight or local heat sources. Heat
ages the crystal and causes loss of sensitivity.
Latex
Terason strongly recommends that health-care professionals identify their latex-sensitive
patients, and refer to the FDA’s March 29, 1991 Medical Alert on Latex products. Be
prepared to treat allergic reactions promptly.
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