4
SpO
2
measuring position must be examined more carefully for some special patient. Do NOT install the
SpO
2
sensor on the finger with edema or vulnerable tissue.
To prevent the risk of the short circuit and to ensure the ECG signal quality, the equipment must be properly
grounded.
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.
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.
All the parts of the Gima Vital Signs 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 ac-
cessories along with the monitor which are provided by the same factory, otherwise, negative effects con-
cerning safety and biocompatibility etc. may be caused.
DO NOT stare at the infrared light of SpO
2
sensor when switch it on, for the infrared may do harm to the
eye.
If the Gima Vital Signs Monitor falls off accidentally, please do NOT operate it before its safety and technical
indexes have been tested minutely and positive testing results obtained.
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.
Alarm limits should not be set to exceed the measuring range, or the alarm system will not generate alarm
signals because of no alarm condition. Refer to the Technical Specification for detailed measuring range.
Please peruse the relative content about the clinical restrictions and contraindication.
When disposing of the Gima Vital Signs Monitor and its accessories, the local law should be followed.
Do not replace the built-in battery when the device is at working state.
