Continuous Sleep Oxygen Monitor, Pulse Oximeter | Wearpulse
User Manual for Checkme models including: O2 Max Smart Wrist Pulse Oximeter, O2 Max, Smart Wrist Pulse Oximeter, Wrist Pulse Oximeter, Pulse Oximeter, Oximeter
User Guide (PDF) wearpulse Viatomtech Continuous,Wrist,Pulse,Oximeter,,Blood,Oxygen,Saturation,Monitor,with,Smart,reminder,,Bluetooth,,72,Hours,Endurance,Tracking,SpO2,and,Pulse,Rate,,Checkme,O2,Max,with,PC,Software,&,APP,,
Wearpulse Continuous Wrist Pulse Oximeter, Blood Oxygen Saturation Monitor with Smart reminder, Bluetooth, 72 Hours Endurance Tracking SpO2 and Pulse Rate, Checkme O2 Max with PC Software & APP : Industrial & Scientific
Vihealth App Manual - Look for signs of illness, treatments, and healthy foods and recipes
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DocumentDocumentCheckme O2 Max Smart Wrist Pulse Oximeter User Manual 1. Introduction 1.1 Intended Use This product is intended to be used for measuring, displaying and storing of pulse oxygen level (SpO2) heart rate and motion of adults. App can show the oxygen level, heart rate; get record, display results and report. It's not a medical device. This device is for Sports and Aviation use only and not intended for medical use. Note: The data and results provided by this device are for pre-check screening purpose only and cannot be directly used for diagnostic or treatment. The data provided by the APP and PC software (optional) is not intended for diagnosis or treatment purpose, always consult your doctor for any health condition. Warnings and Cautionary Advices · DO NOT squeeze the sensor or apply excessive force on the sensor & cable. Do not use this device during MRI examination. Never submerge the device in water or other liquids. Do not clean the device with acetone or other volatile solutions. Do not place this device in pressure vessels or gas sterilization device. Consult your doctor immediately if you experience symptoms that could indicate acute disease. Do not self-diagnose or self-medicate on the basis of this device without consulting your doctor. In particular, do not start taking any new medication or change the type and/or dosage of any existing medication without prior approval. Use only cables, sensors and other accessories specified in this manual. Prolonged using may increase the risk of undesirable changes in skin characteristics, such as irritation, reddening, blistering or burns. Check the oxygen level sensor application site every 6-8 hours to determine the positioning of the sensor and the circulation and skin sensitivity of the user. User sensitivity varies depending on personal status or skin condition. For users with poor peripheral blood circulation or sensitive skin, inspect the sensor site more frequently. Functional tester cannot be used to assess the accuracy of an oxygen level sensor or a device. This device is designed to determine the arterial oxygen saturation percentage of functional hemoglobin. Factors that may degrade pulse oximeter performance or affect the accuracy of the measurement include the following: - excess ambient light - excessive motion - electrosurgical interference - blood flow restrictors (arterial catheters, blood pressure cuffs, infusion lines, etc.) - moisture in the sensor - improperly applied sensor - incorrect sensor type - poor pulse quality - venous pulsations - anemia or low hemoglobin -concentrations - cardiogreen and other -intravascular dyes - carboxyhemoglobin - methemoglobin - dysfunctional hemoglobi 1.2 Guide to Symbols Symbol SN IP22 Fingertip Oximeter User Manual Description Manufacturer Date of manufacture Serial number MRI unsafe. Presents hazards in all MR environments as device contains strongly ferromagnetic materials. Indicate separate collection for electrical and electronic equipment (WEEE). Protected against spraying water and against access to hazardous parts with a tool, per IEC 60529. Follow Instructions for Use. Type BF-Applied Part Warning and Caution! No alarm system. This product complies with the rules and regulations of the Federal Communication Commission. Non-ionizing radiation This product complies with verpackG. 1.3 Unpacking Main Unit × 1 Ring Sensor × 1 Cable × 1 User Manual × 1 2. Using the Device 2.1 Overview 1. Pulse oximeter 2. Wristband 3. Sensor interface / charging interface 4. Power button 5. Oxygen level sensor Screen display item description: Oxygen level Heart rate Wear the sensor Time Remaining battery capacity Reminder is on Reminder is off Bluetooth is connecting 2.2 Charging Charge the battery before using. Use the charge cable to charge the battery of device in the USB Port of the computer or with USB charging adapter. After being fully charged, the device will power off automatically. 2.3 Power on/off Power on: Press the button for 1 second to turn on the device. Power off: Automatically power off: The device will turn off automatically in 2 minutes if no measurement, no operation or without App connection. Manually power off: You can press the button for about 2 seconds to turn off. 2.4 Take the first recording Start. Wear the device and the Ring Sensor, press the button to power on. And keep yourself in the quiet environment. (For the sake of clarity, recommended the user wear the device watch on their left wrist and put the ring sensor on the thumb. If it is too tight, try another finger. Avoid being loose.) Stop. After the record, take off the Ring Sensor (and the device), the recording will be saved after the countdown. (If the working time is less than 1 minute, the data will not be saved.) Note: · Please avoid excessive motion for the sensed finger during recording and avoid any strong ambient light condition. 2.5 Stop working & sync data Take off the sensor, the countdown will begin. During the countdown, if you wear the sensor again, the record will be resumed. After the countdown, the data will be ready for sync. Note: The duration of the recording is 1mins~10 hours. And the device can collect and store maximum 4 recording, when the 5th recording coming, the first recording will be will covered. Sync data to the ViHealth App You can Sync the data to your app after the countdown or next time after you turn on the device. Note: Refer the ViHealth app manual for more details. 2.5.1 How to find the Serial Number 1Detach the main unit from wristband. 2Flip the main unit over, the series number is printed on the label of product. Note: The serial number is on the back of the device. 2.6 How to synchronize the time of the device The time of the device will be automatically synchronized with the network time on your smart device after connected with the app. Note: Refer the ViHealth app manual for more details. 2.7 Reminder When the device detects low oxygen level or abnormal heart rate, it supports triggering reminders. You can customize the reminder after the device power on, or use the App to configure. 2.8 Download App App name: ViHealth iOS: App Store Android: Google Play Compatibility The device is compatible with iOS versions 9.0+ and Android versions 5.0+. Refer the ViHealth app manual for more details. 2.9 Bluetooth Connection The device Bluetooth will be enabled automatically when the device is on. Note: DO NOT PAIR in the settings of your smart device. 3. PC software 3.1 Download the PC Software PC Software: O2 Insight Pro Download from: https://iwearpulse.com/pages/app- download Install the software on Windows PC or Mac. 3.2 How to connect the device to PC 1. Turn on device, connect the device to PC USB port with the supplied Cable of data. 2. Open the PC software, download data from the device. 3. With the optional PC software,You can view and print report, which can also be exported as PDF or CSV files. 3.3 How to connect the device to Mac 1. Turn on device, and turn on the Bluetooth of the Mac. 2. Open the "O2 Insight Pro" software and click the "Connect" on the screen. Choose your device to connect. 3. Then click the "download" on the screen. Then the data will sync with your Mac. 4. You can view and print report, which can also be exported as PDF or CSV files. 4. Maintenance 4.1 Cleaning Use a soft cloth moistened with water or alcohol to clean the device surface. 4.2 Battery To keep the battery in good condition, charge the battery every 6 months when the device is not in use. 5. Troubleshooting Problem Device does not turn on or no response. Possible Cause Battery may be low. Unexpected software condition Device might be damaged. The app cannot find the device. The Bluetooth of your phone is off. Possible Solution Charge battery and try again. Press the button for about 10 seconds to reset Please contact your local distributor. Turn on the Bluetooth in the phone. 6. Specifications Classifications MDD, 93/42/EEC EC Directive R&TTE, 1999/5/EC ROHS 2.0, 2011/65/EU Degree protection against electrical shock Type BF Environmental Item Operating Storage Temperature 5 to 40°C -25 to 70°C Relative humidity (noncondensing) 10% to 95% 10% to 95% Barometric 700 to 1060 700 to 1060 hPa hPa Degree of dust & water resistance IP22 Physical Weight 18 g (main unit) Display Wireless OLED Bluetooth 4.0 BLE Vibrator Built in Power Supply Charge input: DC 5V ±10% Battery type Rechargeable lithium-polymer battery Battery run time 72 hours Charge time 2.5 hours Oxygen level Standards Meet standards of ISO 80601-2-61 Measurement accuracy verification: The oxygen level accuracy has been verified in human experiments by comparing with arterial blood sample reference measured with a CO-oximeter. The heart rate accuracy has been verified by Emulator. Pulse oximeter measurement are statistically distributed and about two-thirds of the measurements are expected to come within the specified accuracy range compared to CO-oximeter measurements. Oxygen level range 70% to 100% Oxygen level Accuracy (Arms) 80-100%:±2%, 70-79%:±3% PR range 30 to 250 bpm PR accuracy ±2 bpm or ±2%whichever is greater Wave length 660-940nm Output power Red/Infrared: 3mW max. avg. Storage Capacity 4 records,10 hours for each Mobile APP iOS iOS 9.0 or above, iPhone 4s/iPad 3 Android or above Android 5.0 or above, with Bluetooth 4.0 BLE Fingertip Oximeter User Manual 7. FCC Statement FCC Warning: FCC ID: 2ADXK-1600 Any Changes or modifications not expressly approved by the party responsible for compliance could void the user's authority to operate the equipment. 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. Note: This equipment has been tested and found to comply with the limits for a Class B digital device, pursuant to part 15 of the FCC Rules. These limits are designed to provide reasonable protection against harmful interference in a residential installation. This equipment generates uses and can radiate radio frequency energy and, if not installed and used in accordance with the instructions, may cause harmful interference to radio communications. However, there is no guarantee that interference will not occur in a particular installation. If this equipment does cause harmful interference to radio or television reception, which can be determined by turning the equipment off and on, the user is encouraged to try to correct the interference by one or more of the following measures: -Reorient or relocate the receiving antenna. -Increase the separation between the equipment and receiver. -Connect the equipment into an outlet on a circuit different from that to which the receiver is connected. -Consult the dealer or an experienced radio/TV technician for help. The device has been evaluated to meet general RF exposure requirement. The device can be used in portable exposure condition without restriction. 8. Electromagnetic Compatibility The device meets the requirements of EN 60601-1-2. Warnings and Cautions · Using accessories other than those specified in this manual may result in increased electromagnetic emission or decreased electromagnetic immunity of the equipment. · The device or its components should not be used adjacent to or stacked with other equipment. · The device needs special precautions regarding EMC and needs to be installed and put into service according to the EMC information provided below. · Other devices may interfere with this device even though they meet the requirements of CISPR. · When the inputted signal is below the minimum amplitude provided in technical specifications, erroneous measurements could result. · Portable and mobile communication equipment may affect the performance of this device. Other devices that have RF transmitter or source may affect this device (e.g. cell phones, PDAs, and PCs with wireless function). Table 1 Guidance and manufacturer's declaration-electromagnetic emissions 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. Emissions test Compliance Electromagnetic environmentguidance RF emissions CISPR 11 Group 1 The device uses RF energy only for its internal function. Therefore, its RF emissions are very low and are not likely to cause any interference in nearby electronic equipment. RF emissions CISPR 11 Harmonic emissions IEC61000-3-2 Voltage fluctuations/flicker emissions IEC61000-3-3 Class B N/A N/A The device is suitable for use in all establishments, including domestic establishments and those directly connected to the public low-voltage power supply network that supplies buildings used for domestic purposes. Table 2 Guidance and manufacturer's declaration electromagnetic immunity 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. Immunity test IEC60601 test level Compliance level Electromagnetic environment guidance Floors should be wood, concrete or ceramic tile. If floors are covered with synthetic material, the relative humidity should be at least 30%. If ESD interfere with the Electrostatic discharge(ESD) IEC61000-4-2 ±8 kV contact ±15kV air ±8 kV contact ±15kV air operation of equipment, counter measurements such as wrist strap, grounding shall be considered. Electrical fast transient/ burst IEC61000-4-4 ±2kV for power supply lines ±1 kV for input/output lines ±2kV for power supply lines ±1 kV for input/output lines The quality of the power supply should meet the requirements of a typical commercial (initial power supply). Surge ±1kV line to line IEC 61000-4-5 ±2kV line to earth Voltage dips, short interruptions and voltage variations on power supply input lines IEC 61000-411 0% UT (100% dip in UT) for 0.5 cycle 0% UT (100% dip in UT) for 1 cycle 70% UT (30% dip in UT) for 25/30 cycles 0% UT (100% dip in UT) for 250/300 cycles ±1kV line to line ±2kV line to earth The quality of the power supply should meet the requirements of a typical commercial. 0% UT (100% dip in UT) for 0.5 cycle 0% UT (100% dip in UT) for 1 cycle 70% UT (30% dip in UT) for 25/30 cycles 0% UT (100% dip in UT) for 250/300 The quality of the power supply should meet the requirements of a typical commercial. If the user of this product needs to continue poerating during power interruption,it is recommended to use uninterruptible power supply or battery power. cycles Power frequency (50/60Hz) magnetic field IEC61000-4-8 30 A/m 30 A/m Power frequency magnetic fields should be at levels characteristic of a typical location in a typical commercial or hospital environment. NOTE : UT is the AC mains voltage prior to application of the test level. Table 3 Guidance and manufacturer's declaration electromagnetic immunity 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. Immunity IEC60601 Compliance Electromagnetic test test level level environment -guidance Portable and mobile RF communications equipment should be used no closer to any part of the device, including cables, than the recommended separation distance calculated from the Conducted 3 Vrms equation applicable to the RF 150 kHz to N/A frequency of the transmitter. IEC61000-4- 80 MHz(6V Recommended separation 6 in ISM and distance amateur d=1.2 P radio bands d=1.2 P 80MHz to 800MHz between 0.15MHz d=2.3 P 800MHz to 2.5GHz Where P is the maximum and output power rating of the 80MHz) transmitter in watts (W) according to the transmitter manufacturer and d is the Radiated RF recommended separation IEC61000-4- 3 V/m 10 V/m distance in metres (m). 3 80 MHz to Field strengths from fixed RF 2.5 GHz transmitters, as determined by an electromagnetic site survey ,a should be less than the compliance level in each frequency range .b Interference may occur in the vicinity of equipment marked with the following symbol. Recommended separation distances between portable and mobile RF communications equipment and the Pulse Oximeter The Pulse Oximeter is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled. The customer or the user of the Pulse Oximeter can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment (transmitters) and the Pulse Oximeter as recommended below, according to the maximum output power of the communications equipment. Rated Separation distance according to frequency of maximum transmitter M(Meters) output power 150kHz to 80MHz to 800MHz 80MHz to of transmitter 80MHz d=1.16 P 2,5GHz W(Watts) d=1.16 P d=2.33 P 0,01 0.12 0.12 0.23 0,1 0.38 0.38 0.73 1 1.2 1.2 2.3 10 3.8 3.8 7.3 100 12 12 23 For transmitters rated at a maximum output power not listed above, the recommended separation distance d in meters (m) can be estimated using the equation applicable to the frequency of the transmitter, where p is the maximum output power rating of the transmitter in watts (W) according to the transmitter manufacturer. NOTE 1 At 80 MHz and 800 MHz, the separation distance for the higher frequency range applies. NOTE 2 These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from structures, objects and people. Manufacturer Shenzhen Viatom Technology Co., Ltd. 4E, Building 3, Tingwei Industrial Park, No 6 Liufang Road, Block 67, Xin`an Street, Baoan District, Shenzhen, 518101, Guangdong, P.R.China www.iwearpulse.com Version: A Date: Nov. 24, 2022 PN:255-05862-00 Contents of this manual are subject to changes without prior notice. ©Copyright 2020 Shenzhen Viatom Technology Co., Ltd. All rights reserved. Model: Oxiband