V1.0K3 PULSE OXIMETER INSTRUCTION MANUAL Copyright Our company owns all rights of this unpublished work and intends to maintain it as a confidential work. We may also seek to maintain this work as an unpublished copyright. This publication is to be used solely for the purpose of reference or operation of our device. No part of this work can be disseminated for other purposes.
V1.0K3 PULSE OXIMETER INSTRUCTION MANUAL Contents 1 Introduction ............................................................................................. 2 1.1 Brief Introduction................................................................................................ 2 1.2 Safety Information .............................................................................................. 2 1.3 Intended use............................................................................................
V1.0K3 PULSE OXIMETER INSTRUCTION MANUAL 1 Introduction 1.1 Brief Introduction Thank you for purchasing the pulse oximeter. The main functions of the device include Haemoglobin Saturation (SpO2) and pulse rate (PR) measurements, visual and audible alarm, batteries charging, data storage and review, USB cable and Bluetooth® for data transmission, etc. Please read this manual carefully before using the device. Note: The illustrations applied in the manual may differ slightly from the actual unit. 1.
V1.0K3 PULSE OXIMETER INSTRUCTION MANUAL skin deterioration, and discomfort. z 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 950 and IEC 601-1-1. Any input/output device should follow the protocol of IEC 601-1-1.
V1.0K3 PULSE OXIMETER INSTRUCTION MANUAL z Remove fingernail polish or artificial fingernails before applying SpO2 probes. Fingernail polish or artificial fingernails may lead to inaccurate SpO2 readings. z Optical cross talk can occur when two or more probes are located in adjoining area. It can be eliminated by covering each site with opaque material. Optical cross talk may adversely affect the accuracy of the SpO2 readings.
V1.0K3 PULSE OXIMETER INSTRUCTION MANUAL levels of such interference due to close proximity or strength of a source, may result in disruption of performance of this device. This apparatus complies with the IEC 60601-1-2 international standard. The requirements of this international standard are: CISPR11, GROP1, and CLASS B. 1.
V1.0K3 PULSE OXIMETER INSTRUCTION MANUAL 1.6 Product Features Simple to use and easy to operate. Portable and compact in design. TFT display screen with adjustable backlight. Up to 127 patients’ ID and 72-hour records can be saved. Visual and three-level audible alarms, low battery power alarm. Data transfer to PC by USB cable or Bluetooth®. Powered by four AA alkaline/Ni-MH batteries/power adapter. Battery charge function with adapter (optional).
V1.0K3 PULSE OXIMETER INSTRUCTION MANUAL Fig.2-1 Description of Fig.2-1： (1) Fixing clip for the SpO2 probe. (2) Displaying screen. (3) Print Button: Press this button to turn on/off the function of printing. (4) OK Button: Press this button to enter menu items or confirm the selection/setting.
V1.0K3 PULSE OXIMETER INSTRUCTION MANUAL (5) Up Button: Press this button shortly to increase the value by one unit. You can press and hold the button extendedly to speed up the adjustment of values. (6) Alarm inhibition button: Press this button to close alarm sound for 120 seconds. You can open the alarm sound in the process of alarm inhibition by pressing the button again. (7) Down button: Press this button shortly to decrease the value by one unit.
V1.0K3 PULSE OXIMETER INSTRUCTION MANUAL 2.2 Rear Panel (1) Paper Feed button: when the printing function is on, press this button you can start printing. (2) Outlet: the outlet for printing paper. (3) The groove for installing the printing paper. (4) The cover of battery compartment. Fig.2-2 2.3 Power Supply The device can be powered by 4 AA alkaline batteries, Ni-MH batteries or power adapter. 2.3.
V1.0K3 PULSE OXIMETER INSTRUCTION MANUAL Fig.2-3 Warnings! DO NOT USE Ni-MH rechargeable and alkaline batteries together, otherwise, that may damage the device or injury users. Make sure the polarities of the batteries are correct. 3) Close the battery cover. Battery life When the battery power is lower than 4.5V±0.1V the battery indicator will become empty and at the same time its frame will become red, which means little of battery capacity remains.
V1.0K3 PULSE OXIMETER INSTRUCTION MANUAL Do not use batteries of different types together. Do not use new and used batteries together. Dispose of batteries in accordance with the local ordinances and regulations. Regular maintenance of rechargeable batteries is required, such as periodic charge and discharge. The charging time shouldn’t be too long, otherwise, it may reduce batteries performance and shorten batteries’ life. 2.3.
V1.0K3 PULSE OXIMETER INSTRUCTION MANUAL shown in Fig.3-1. When the SpO2 probe is connected well, please set the fixing clip up to ensure the probe well connected. Fig.3-1 The indicator will be shown on the display screen when the probe is well connected. If the probe is disconnected from the unit, the indicator and the prompt “Probe Off！！ ！” will appear in the status column. The socket is also used for USB cable connected with the PC for data transmission.
V1.0K3 PULSE OXIMETER INSTRUCTION MANUAL Fig.4-1 2) Press the Down button to select the “Date and Time” item, and then press the Menu button to enter the time setup screen, refer to Fig.4-2. Fig.4-2 Pick different sub-items to set and press the OK button to highlight it and then using the Up or Down button to adjust the value. At last, press the OK button to confirm your settings. 4.2 ID number Setting Enter the “User ID Setting” item from the main menu screen, refer to Fig.4-3.
V1.0K3 PULSE OXIMETER INSTRUCTION MANUAL that “Cannot change!!!”, if you attempt to change it when taking a measurement. Fig.
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V1.0K3 PULSE OXIMETER INSTRUCTION MANUAL Fig.5-2 Digital display Fig.5-3 Wave display Status bar 1: The status of the oximeter is shown on the bar (Measure… , Finger out!!, Probe off!! and so on). Status bar 2: If the measured SpO2% or PR value exceeds the alarm limits, there will be corresponding information. SpO2%: SpO2 area of display ◆It shows the oxygen saturation level of functional hemoglobin during normal measurement.
V1.0K3 PULSE OXIMETER INSTRUCTION MANUAL ◆The color of the PR value will become yellow when the PR value exceeds the alarm limits. ◆It shows three dashes throughout probe off and finger out conditions. 15:00: The current time. 6 Other Settings 6.1 Alarm Setting From the main menu, select and enter the “Alarm setting” screen, refer to Fig.6-1. 1) SpO2 alarm setup To set SpO2 alarm high limit in the “Alarm setting” screen, press the Up or Down button to select the “High limit（SpO2）”.
V1.0K3 PULSE OXIMETER INSTRUCTION MANUAL with “×”. Note: Please caution the alarm off item, it may cause damages to users. ALARM PRIORITY Alarms of the oximeter include technical and physiological alarms. All the three priorities are divided by built-in module and can not be changed by users. High priority: indicates the patient is in the very dangerous situation. Medium priority: indicates the warnings should be paid attention to. Low priority: indicates the technical alarm caused by the device itself.
V1.0K3 PULSE OXIMETER INSTRUCTION MANUAL manually for free space. Fig.6-2 6.2.1 Data Review Pick and enter the “Data Review” sub-item, the screen as shown in Fig.6-3 will appear. You can move the rolling bar to view all the records that have saved in the unit by pressing the Up or Down button. Press the OK button, a dialog box will pop up, refer to Fig.6-4.
V1.0K3 PULSE OXIMETER INSTRUCTION MANUAL Press the OK button, a dialog box will pop up, refer to Fig.6-6. After selecting a ID number, press the Up or Down button to select “Delete” or “Review” and then press the OK button to confirm, you can delete or review all the SpO2 trends saved under this ID. Fig. 6-5 Fig. 6-6 6.2.3 PR Trend The specific operations are as the same as “SpO2 Trend”, please refer to 6.2.2 SpO2 Trend. 6.2.
V1.0K3 PULSE OXIMETER INSTRUCTION MANUAL Fig.6-7 In the data management screen, the upper half screen will display the maximum, minimum and average values of SpO2 and PR for the current ID. Refer to Fig.6-8. Fig.6-8 6.2.5 Copy to SD The SD card is only as a transfer media for data transmission from the unit to PC. By entering this item you can copy the saved data in the unit to the inserted SD card manually, and then through the SD card reader transfer data to PC.
V1.0K3 PULSE OXIMETER INSTRUCTION MANUAL 6.3 System Setting From the main menu, select and enter the System Setting screen, refer to Fig.6-9&6-10. Press the Up or Down button to pick the different sub-items to set and press the Select button to enter. Fig.6-9 Fig.6-10 6.3.1 Brightness Pick and enter the Brightness sub-item from the System Setting screen, and set the brightness level and bright time. Brightness level: 1-7 Bright time: ON, 15, 30, 45, 60, 75, 90,105,120 seconds.
V1.0K3 PULSE OXIMETER INSTRUCTION MANUAL The beep on or off can be displayed in the main screen by the symbol and . 6.3.4 Display Mode You can set the display mode Digital or Wave by entering the Display Mode sub-item. First press the OK button to highlight it and then press the Up or Down button to select Digital or Wave item, last press the OK button again to confirm your selection. This two display modes are shown in Fig.5-2&5-3. 6.3.
V1.0K3 3. PULSE OXIMETER INSTRUCTION MANUAL Press the Paper Feed button on the top of the rear panel, then the unit will begin printing. You can end the current printing by pressing the PRINT button. If the printing paper is not installed, the steps for printing are as follows: 1. Set the Print ON in the system setting menu firstly. 2. Press the PRINT button on the front panel secondly. 3. Press the Paper Feed button and then begin installing paper as shown in Fig.6-11. 4.
V1.0K3 PULSE OXIMETER INSTRUCTION MANUAL 6.3.9 About Enter the About screen from the System Setting screen, the version of software is displayed. 7 Maintain and Repair 7.1 Maintenance Use only the substances approved by us and methods listed in this chapter to clean or disinfect your equipment. Warranty does not cover damage caused by unapproved substances or methods. We make no claims regarding the efficacy of the listed chemicals or methods as a means for controlling infection.
V1.0K3 PULSE OXIMETER INSTRUCTION MANUAL z Make sure that only specified accessories are applied. z Inspect if the alarm system functions correctly. z Make sure that the batteries meet the performance requirements. z Make sure that the pulse oximeter is in good working condition. In case of any damage or abnormity, do not use the pulse oximeter. Contact your hospital’s biomedical engineers or your service personnel immediately. Cleaning Your equipment should be cleaned on a regular basis.
V1.0K3 PULSE OXIMETER INSTRUCTION MANUAL Battery maintenance ○Please take out battery if you will not use the monitor for a long time. ○Please charge the battery fully if you will not use it for a long time. ○Please charge over 14 hours at the first time, or may reduce the battery life. If any abnormal phenomena occurs, should stop using immediately and reuse after inspection by technical person. f) Inspect the equipment and accessories for mechanical and functional damages.
V1.0K3 PULSE OXIMETER INSTRUCTION MANUAL 7.3.4 SpO2 & PR Alarm Verification a). Connect SpO2 Probe to the SpO2 connector on the oximeter. b). Insert the operator’s finger into the finger probe, the SpO2 measured value of healthy person should be more than 96%. c). Set the SpO2 high limit as 90, low limit as 80. d). Verify the SpO2 visual and auditory alarms, the backgroud color of the SpO2 data should be red and "dudu" voice should be heard. 7.
V1.0K3 PULSE OXIMETER INSTRUCTION MANUAL labor and capital bother, strike and stop-working etc. b) No-service offer The corresponding fee and insurance fee of disassembly, refurbishment, repackaging and conveying of the oximeter or the part of it doesn’t comply with the instruction manual. The damage is caused by the third company which is not commended by our company adjusting, installing or replacing the parts of the oximeter.
V1.0K3 PULSE OXIMETER INSTRUCTION MANUAL ●Not-original package lead to oximeter during transportation ●Not-professional person operation leads to oximeter failure. Not our company professionals or authorized personnel disassemble oximeter and lead to oximeter failure. ●Not carefully read manual and so wrong operation lead to oximeter damage and failure. 7.5.
V1.0K3 PULSE OXIMETER INSTRUCTION MANUAL personnel authorized by our company. Display Data: SpO2%, PR, pulse bar, plethysmogram; Others: connection status of probe and other alarm information; Data update time: less than 5 seconds; SpO2 Display range: 0%~100% Measurement range: 70%~100% Resolution: 1% Accuracy: 70-100%：±3%； ＜70%：unspecified； Probe LED Specifications: Wavelength 660±2nm 940±10nm RED IR Radiant Power 1.8mW 2.
V1.0K3 PULSE OXIMETER INSTRUCTION MANUAL Working Distance: 20-100m Interface: USB 1.1 Operation system: Windows98®, 2000®, XP® Classification According to the type of protection against electric shock: Internal powered equipment and class II equipment; According to the degree of protection against electric shock: Type BF applied part; According to the degree of protection against ingress of water： IPX1; Operation mode: Continuous running mode.
V1.0K3 PULSE OXIMETER INSTRUCTION MANUAL 6. One roll of Printing paper. 7. One Bluetooth® adapter. 8. One 2GB SD card. z Optional accessories: 1. One Power adapter. 2. Four AA Ni-MH batteries. 3. One disposable sponge wrap sensor for adult: Model: M-50J. Manufacturer address：Beijing Choice Electronic Technology Co.，Ltd. Bailangyuan Building B Rm.
FCC ID: WWIMD300K3 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. changes or modifications not expressly approved by the party responsible for compliance could void the user's authority to operate the equipment.
