Gima 35132 Manual De Uso página 88

M DO NOT take blood pressure measurement from a limb receiving ongoing transfusion or intubation or
skin lesion area, otherwise, damages may be caused to the limb.
M Continuous use of SpO
micro-circulatory problem. It is recommended that the sensor should NOT be applied to the same
place for over two hours, change the measuring site periodically if necessary.
M SpO measuring position must be examined more carefully for some special patient. Do NOT install
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the SpO sensor on the finger with edema or vulnerable tissue.
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M To prevent the risk of the short circuit and to ensure the ECG signal quality, the equipment must be
properly grounded.
M Although biocompatibility tests have been performed on all the applied parts, some exceptional
allergic patients may still have anaphylaxis. Do NOT apply to those who have anaphylaxis.
M All the connecting cables and rubber tubes of the applying parts should be kept away from the
patient' s cervix to prevent any possible suffocation of the patient.
M All the parts of the monitor should NOT be replaced at will. If necessary, please use the components
provided by the manufacturer or those that are of the same model and standards as the accessories
along with the monitor which are provided by the same factory, otherwise, negative effects
concerning safety and biocompatibility etc. may be caused. No modification of this device is
allowed.
M If any operator requests more information such as circuit diagrams, parts list and product
descriptions, for repairs carried out by qualified technical personal, please contact us.
M DO NOT stare at the infrared light of SpO
the eye.
M If the monitor falls off accidentally, please do NOT operate it before its safety and technical indexes
have been tested minutely and positive testing results obtained.
M It is recommended to take the blood pressure measurement manually. The automatic or continuous
mode should be used at the presence of a doctor/nurse.
M Please peruse the relative content about the clinical restrictions and contraindication.
M When disposing of the monitor and its accessories, the local law should be followed.
M Substitution of a component different from that supplied might result in measurement error.
M It is recommended that the clinical operator regularly test device and accessories. And the visual
and auditory alarm signals can be checked by intentionally disconnect accessories.
M Do not allow service or maintenance the device while used in patient.
M Please do not to position the device so that it is difficult to operate mains plug.
User Manual for Vital Signs Monitor
sensor may result in discomfort or pain, especially for those with
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sensor when switch it on, for the infrared may do harm to
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III