Compatible for GE Oxitip Patient Monitors, Disposable SPO2 Probe Sensor, SPO2 Finger Sensor, Blood oxygen Saturation Data Monitoring

1 Pieces/Package

1. Specifications: DIS01 Disposable sensor with Bandage (SIZE:A/B/C/D) DIS02 Disposable sensor with PE-Sponge(SIZE:A/B/C/D) DIS03 Disposable sensor with blue Sponge (SIZE:A/B/C/D) DIS04 Disposable sensor with Non-woven (SIZE:A/B/C/D) A:adult B:pediatric C:infant D:neonate

2. Working principle The SpO2 measurement is based on the absorption of pulse blood oxygen to red and infrared light by means of sensor and SpO2 measuring unit(Pulse Oximeter). The light-electronic transducer in sensor converts the pulse red and infrared light modulated by pulse blood oxygen into electrical signal, the signal is processed by hardware and software of SpO2 measuring unit(Pulse Oximeter). The pleth curve Or(and) numeral value of SpO2 will be obtained.

3. Warning 1) User should verify the compatibility of the monitor, sensor, and cable before use, otherwise cause patient injury. 2) Check the site every 2 hours (more frequently if perfusion is poor). 4) Routinely check to ensure adequate distal circulation to the sensor site. 3) Carefully route cables to reduce any possibility of patient entanglement or strangulation. 4) Patient conditions (such as reddening, blistering, skin discoloration, ischemic skin necrosis, and skin erosion) may warrant changing the site frequently or using a different style of sensor. 5) Do not use the sensor if the sensor or the cable appears damaged. 6) This device is not intended for use in a magnetic resonance imaging (MRI) environment. 7) Conditions that may cause inaccurate reading and impact alarms include interfering substances, excessive ambient light, electrical interference, excessive motion, low perfusion, low signal strength, incorrect sensor placement, poor sensor fit, and movement of the sensor on the patient. 8) Do not use a blood pressure cuff or arterial blood pressure measurement device on the same limb as the sensor site. 9) It is possible for any device to malfunction; therefore, always verify unusual data by performing a formal patient assessment.