I-Tech Pulse Oximeter-Saturimeter 30011 - LOX100A

DESCRIPTION:

Fingertip pulse oximeter intended for home or hospital use for the non-invasive measurement of oxygen saturation, heart rate and perfusion index.

The device can be used in children and adults.

EQUIPMENT

• Device with OLED screen
• 2 AAA size batteries
• Safety strap
• user manual

FUNCTIONS and CHARACTERISTICS

• Detection of the degree of oxygen saturation in the blood (SpO2)
• Heart Rate (PR) Detection
• OLED display
• SpO2, heart rate, pulse bar and perfusion index indication
• If the SpO2 and PR values exceed their set limits, the device will periodically emit beeps and the numerical value will flash to warn the user.
• Auto power off if finger not inserted for 8 seconds
• Battery charge indicator
• Equipped with 4 different user screen options.
• Suitable for adults and children
• Medical device CE0123

SpO2:

• Measuring range: 70% ~ 99%%
• Resolution: 1%
• Accuracy 80% ~ 99% ±2%; 70% ~ 79% ±3%; No requirement for accuracy less than 70%

Heart rate:

• Measuring range: 30 bpm ~ 240 bpm
• Resolution 1 bpm
• Measurement accuracy: 30 bpm ~ 240 bpm, ±2 bpm or ±2% (whichever is greater)

Dimensions and weight:

• Size: 69×35×29 mm
• Weight: 60 gr (with batteries)

Warnings:

1. Please read the User Manual carefully before use.
2. The product cannot be used for continuous measurement.
3. Electrosurgical devices and defibrillators may impair the use of this device.
4. The product should not be used in combination with MRI or CT equipment.
5. Do not squeeze, crush, or apply excessive pressure to the silicone pad during use.
6. The product must not be used in flammable or explosive environments.

7. The product plays a supporting role in patient assessment. A definitive diagnosis should be made based on clinical manifestations and symptoms.

8. For long-term use, the test site may need to be changed periodically. The patient's skin integrity and circulatory status should be checked every 2 hours and adjustments made accordingly.
9. Disinfecting by autoclaving, vinyl oxide, or immersing the sensor in a disinfectant solution will damage the device and cause incorrect readings.
10. The device specified in this manual together with its accessories and batteries must comply with local laws and regulations.
11. This device complies with the electromagnetic compatibility requirements for medical electrical products or systems set out in IEC 60601-1-2. Radio transmission equipment or other electromagnetic interference may affect the performance of this device.
12. Portable radio communications equipment may affect the performance of this device.
13. The device must not be used in close proximity to other radio equipment or placed on top of any other equipment.
14. Use of this device is not recommended during patient transport, such as in ambulances or other vehicles.
15. Do not disassemble or attempt to repair this device without prior authorization.
16. The materials that will come into contact with the patient are composed of silica gel pads compliant with ISO 10993 standard.
17. When in contact with the patient, the temperature should not exceed 40°C. The maximum recommended application time should not exceed 2 hours.
18. The device is not intended for patients weighing less than 20kg, pregnant or breastfeeding women.
19. Dispose of batteries in accordance with local regulations. Never throw batteries into a fire!
20. This device does not have audible warnings.
21. The device is ready for its intended use when the ambient temperature reaches 40°C. The time required to reach room temperature from the minimum/maximum storage temperature is approximately 15±5 minutes.

• EAN
  6971393240257