1. Before use, carefully read the manual.
2. Do not use the pulse oximeter:
-If you are allergic to rubber products.
-If the device or finger is damp.
-During MRI or CT scan.
-While taking a blood pressure measurement on the arm.
-Nail polish, dirty, coating fingers and false nails applied fingers.
-Fingers with anatomical changes, edemas, scars or burns.
-Too big finger: the width of finger is over than 20mm and the thickness is over than 15mm.
-Too small finger: the width of finger is less than 10mm and the thickness is less than 5mm.
-Minors under 18 years old.
-The environmental light changes strongly.
-Near flammable or explosive gas mixtures.
3. Extended use may cause pain for people with circulatory disorders. Do not use the pulse oximeter for longer than two hours on one finger.
4. Measurements are for your information only - they are no substitute for a medical examination. If an unexpected reading occurs, the operator can take several more measurements and consult a doctor.
5. Check the pulse oximeter regularly before use to ensure that there is no visible damage and the batteries are still sufficiently charged. In case of doubt, do not use the device and contact customer services or authorized retailer.
6. Do not use any additional parts that are not recommended by the manufacturer.
7. Any circumstances do not open or repair the device by yourself. Failure to comply will result in voiding of the warranty. For repairs, please contact customer services or authorized retailer.
8. Do not look directly inside the housing during the measurement. The red light and the invisible infrared light in the pulse oximeter are harmful to your eyes.
9. This device is not intended for use by people (including children) with restricted physical, sensory or mental skills or a lack of experience or a lack of knowledge, unless they are supervised by a person who has responsibility for their safety or they receive instructions from this person on how to use the device. Children should be supervised around the device to ensure they do not play with it.
10. If the unit has been stored at temperatures below 0℃, leave it in a warm place for about two hours before using it.
11. If the unit has been stored at temperatures above 40 , leave it in a cool place for about two hours before using it.
12. The displays for the pulse bar does not allow the strength of the pulse or circulation to be evaluated at the measurement site. Rather, they are exclusively used to display the current visual signal variation at the measurement site and do not enable diagnostics for the pulse.
13. Operation of the fingertip pulse oximeter may be affected by the use of an electrosurgical unit (ESU).
14. Follow local ordinances and recycling instructions regarding disposal or recycling or the device and device components, including batteries.
15. This equipment complies with IEC 60601-1-2 for electromagnetic compatibility for medical electrical equipment and systems. In healthcare center or other environment, their radio transmission equipment and electromagnetic interference may affect the performance of the oximeter.
16. This equipment is not intended for use during patient transport outside the healthcare facility.
17. When the signal is not stable, the reading may inaccurate. Please do not reference.
18. Portable and mobile RF communications equipment can affect medical electrical equipment.
19. WARNING: Use of this equipment adjacent to or stacked with other equipment should be avoided because it could result in improper operation. If such use is necessary, this equipment and the other equipment should be observed to verify that they are operating normally.
20. WARNING: PORTABLE RF communications equipment (includeing peripherals such as antenna cables and external antennas) should be used no closer than 30cm (12 inches) to any part of Fingertip Pulse Oximeter, including cables specified by the MANUFACTURER. Otherwise, degradation of the performance of this equipment could result.
21. Any serious incident that has occurred in relation to the device should be reported to the manufacture and the competent authority of the Member State in which the user and/or patient is established.
