Medipost-Nutristoma MD300K2 Mode D'emploi page 4

MD300K2
professional health care. Our company will assume no warranty for using this equipment
improperly.
2. Operation of the handheld pulse oximeter may be affected by the use of an electrosurgical
unit (ESU).
3. Sensor malfunction may cause inaccurate data possibly resulting in patient injury or death,
so pay close attention to the sensor and inspect it often.
4. Do not use the handheld pulse oximeter in an MRI or CT environment.
5. Although the pulse oximeter has alarms, it is not suggested for long time continuous
monitoring.
6. Do not use the handheld pulse oximeter in an explosive atmosphere.
7. The handheld pulse oximeter is intended only as an adjunct in patient assessment. It must
be used in conjunction with other methods of assessing clinical signs and symptoms.
8. Check the pulse oximeter sensor application site every half an hour to determine the
positioning of the sensor and circulation and skin sensitivity of the patient.
9. When begin to gauge associated body features please follow the doctor's counseling.
10. When link this equipment to other peripherals, make sure you are sophisticated operator
to handle this device. Any peripherals should be in the light of protocol of IEC 950 and IEC
601-1-1. Any input/output device should be following the protocol of IEC 601-1-1.
11. Do not sterilize the device using autoclaving, ethylene oxide sterilizing, or immersing the
device in liquid. The device is not intended for sterilization.
12. Follow local ordinances and recycling instructions regarding disposal or recycling of the
device and device components, including batteries.
13. This equipment complies with IEC 60601-1-2:2007 for electromagnetic compatibility for
medical electrical equipment and/or systems. However, because of the proliferation of radio-
frequency transmitting equipment and other sources of electrical noise in healthcare and
other environments, it is possible that high levels of such interference due to close proximity
or strength of a source might disrupt the performance of this device.
14. You should operate the equipment according to the EMC information provided in the
accompanying documents.
15. Portable and mobile RF communications equipment can affect medical electrical
equipment.
16. This equipment should not be used adjacent to or stacked with other equipment.
17. This equipment is not intended for use during patient transport outside the healthcare facility.
18. When connecting this device to other peripherals, make sure that you are qualified to
operate this device. Any peripheral must be certified according to the protocol of IEC 60601-1.
Any input/output device should follow the protocol of IEC 60601-1.
Cautions:
1. The pulse oximeter must be able to measure the pulse properly to obtain an accurate
SpO measurement. Verify that nothing is hindering the pulse measurement before relying on
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the SpO measurement.
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2. Worn-out data cables may also cause inaccurate data, so if the data is used as a reference
to treat a patient, pay special attention to data cable and check it more frequently.
3. Do not tangle the SpO
4. Single use accessories should never be reused.
cable with the wires of ES (Electrosurgery) equipment.
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PULSE OXIMETER