Henry Schein MD300K2 Instrucciones De Uso página 5

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 60950 or IEC 60601-1. Any input/output
device should be following the protocol of IEC 60601-1.
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 60601-1-2:2014 for electromagnetic compatibility for medical elec-
trical 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.
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.
19. When using the equipment, the voice of the environment is not greater than 45 db.
Rx only: "Caution: Federal law restricts this device to sale by or on the order of a physician."
Cautions:
1. The pulse oximeter must be able to measure the pulse properly to obtain an accurate SpO
Verify that nothing is hindering the pulse measurement before relying on the SpO
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.
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measurement.
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measurement.
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