Operation Manual Pulse Oximeter SMPO1000-US
Smart Meter Corporation Release date: 28/07/2020 Product Description Version: 1.0 Pulse Oximeter is an important and common device to check oxygen saturation (SpO2) and pulse rate. It’s a small, compact, simple, reliable and durable physiological monitoring device. It contains the mainboard, OLED display and dry batteries. Intended Use The pulse oximeter is a reusable device，and it’s intended for intermittent checks of oxygen saturation and pulse rate for adults in a clinical environment.
Diagram of Measurement Principle Safety Information Anyone who uses the pulse oximeter must receive adequate training before use. The pulse oximeter is only meant to assess patients’ physiological conditions. It must be used in conjunction with clinical symptoms. It is not intended for treatment. When using the pulse oximeter in conjunction with the electrical surgery equipment, the user should ensure safety of the patient.
electricity should be discharged before usage. Try to keep the pulse oximeter away from any radio receivers when it’s in use. If the pulse oximeter uses with configuration which does not pass EMC test, it can enhance electromagnetic radiation or reduce anti-electromagnetic interference performance. Please use the specified configuration. The pulse oximeter should not be in close proximity (or stacked) with other devices.
Display Introduction Battery Installation 1. Hold the product in one hand with the front panel facing the palm. Put the other hand’s big finger on lid’s press sign of the battery compartment, press downwards and push the lid and open it at the same time. The battery compartment is opened as shown in Figure 2. 2. Install batteries into the slots according to the “+” and “-” symbols as shown in Figure 3. Cover the lid onto the battery compartment and push it upwards to make it close.
1. Thread the thinner end of the lanyard through the lanyard hole. The position of the lanyard hole is shown in Figure 4. (Notice: the lanyard hole is on both sides.) 2. Thread the thicker end of the lanyard through the thinner end of the lanyard. Then, pull the thicker end of the lanyard until it’s tight. Figure 4 Directions for use 1. After properly installing two AAA batteries, press lid’s press sign as shown in the Figure 5 and open the clip.
Don’t put the pulse oximeter on extremities with arterial catheter or venous syringe. Don’t perform SpO2 and NIBP measurements on the same arm simultaneously. Obstruction of blood flow during NIBP measurements may adversely affect the reading of the SpO2 value. Don’t use the pulse oximeter to measure patients whose pulse rates are lower than 30bpm (this may cause incorrect results). The well perfusion of measuring instrument should fully cover the test window of the sensor.
and SIM card number, press it again to exit, as shown in Figure 9. Figure 9 c. When there is no finger inserted, the invalid value “ as shown in Figure 10. ” will be displayed on the screen, Figure 10 d. When the measurement is finished and the network is available, the upload procedure will be started automatically, as shown in Figure11, and it will end with success or failed, as shown in Figure12 and Figure13.
Figure 12 Figure 13 e. The product will automatically shut down when there is no finger inserted for more than 10 seconds or after upload is finished. FCC ID label FCC statements: This device complies with part 15 of the FCC Rules. Operation is subject to the following two conditions: (1) This device may not cause harmful interference, and (2) this device must accept any interference received, including interference that may cause undesired operation.
Network Indicator Description Symbol Description SIM card is not inserted No signal Signal is weak Signal is normal Signal is good Signal is perfect Network is unattached Cleaning and Disinfection Do not immerse the oximeters and any relevant accessories in water or disinfectant. We recommend that the product be disinfected only when necessary to avoid long-term damage to the product. Don’t use cleaning agents/disinfectants other than the recommended models.
The standard configuration Pulse Oximeter 1pc Lanyard 1pc The operation manual 1pc Expected service life: 3 years Technical Specifications 1. Display mode: OLED 2. SpO2: Measurement range: 35~100% Accuracy: ±3%（70%~100%） 3. Pulse Rate: Measurement range: 25~250bpm Accuracy: ±2bpm Pulse Rate accuracy has passed the verification and comparison with SpO2 simulator. 4. Low perfusion： Range: 0.5%~20% SpO2 accuracy: ±3% (70%~100%) PR accuracy: 25~250bpm ±2bpm 5.
Wavelength: 666nm/905nm Output power: <0.1mW Arms Specifications 1. SpO2 Arms: SpO2 Range Arms Specification 70% - 80% 1.65 80% - 90% 1.22 90% - 100% 1.11 2.
Troubleshooting Trouble Possible reason solution The SpO2 and PR can’t be displayed normally and the value disappeared. 1. The finger is not properly positioned. 2. The patient’s SpO2 is too low to be detected. 1. Please try again. 2. Try again; Go to a hospital for a diagnosis if you are sure the device works all right. The SpO2 and PR display unstable. 1. The finger is not placed inside enough. 2. The finger is shaking or the testee is moving. 1. Place the finger properly and try again. 2.
Symbol Meaning Symbol Meaning “CAUTIOUS”! Please refer to the operation manual. Type BF Equipment. The product does not contain alarm function. When the end-user wishes to discard this product, it must be sent to separate collection facilities for recovery and recycling. Information of manufacture, including name and address. Date of manufacture. Serial Number. Batch Code. Type Number. IP22 Degrees of protection provided by enclosure.
Appendix A EMC Declaration Guidance and manufacturer’s declaration - electromagnetic emissions for all EQUIPMENT and SYSTEMS Guidance and manufacturer’s declaration - electromagnetic emission The Pulse Oximeter is intended for use in the electromagnetic environment specified below. The customer or the user of the Pulse Oximeter should assure that it is used in such an environment.
a) Discharges shall be applied with no connection to an artificial hand and no connection to PATIENT simulation. PATIENT simulation may be connected after the test as needed in order to verify BASIC SAFETY and ESSENTIAL PERFORMANCE. b) Applies only to ME EQUIPMENT and ME SYSTEMS with magnetically sensitive components or circuitry. c) During the test, the ME EQUIPMENT or ME SYSTEMS may be powered at any NOMINAL input voltage, but with the same frequency as the test signal (see Table 1).
additional test frequency shall be used in the ISM or amateur radio band. This applies to each ISM and amateur radio band within the specified frequency range. - The ISM (industrial, scientific and medical) bands between 0.15 MHz and 80 MHz are 6.765 MHz to 6.795 MHz; 13.553 MHz to 13.567 MHz; 26.957 MHz to 27.283 MHz; and 40.66 MHz to 40.70 MHz. The amateur radio bands between 0.15 MHz and 80 MHz are 1.8 MHz to 2.0 MHz, 3.5 MHz to 4.0 MHz, 5.3 MHz to 5.4 MHz, 7 MHz to 7.3 MHz, 10.1 MHz to 10.
