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Summary of Contents for Byond BPAP Series
- Page 1 Sleep Apnoea Breathing Therapy Equipment BPAP series User Manual Please read it carefully before using this product...
- Page 2 Statement This user manual is for Sleep Apnoea Breathing Therapy Equipment ResPlus BPAP series of Hunan Beyond Medical Technology Co., Ltd. All information contained in this document is owned by Hunan Beyond Medical Technology Co., Ltd. Unless authorized in writing by Hunan Beyond Medical Technology, no reproduction in any way or of any parts of this document is permissible.
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Page 3: Table Of Contents
Contents 1. Introduction ................4 2. Product Model ................ 6 3. Package Accessories ............... 7 4. Device Components ..............7 5. Device Symbols ..............8 6. Device Operation ..............8 7. Humidifier ................10 8. SpO2 Kit ................11 9. Parameter Settings ..............12 10. -
Page 4: Introduction
1. Introduction 1.1 Intended use The ResPlus Sleep Apnoea Breathing Therapy Equipment is a Bi-level Positive Airway Pressure device which is intended to provide non-invasive ventilation for patients with obstructive sleep apnea (OSA) for both home and hospital treatment. The device is to be used on the instruction of a licensed health care professional or doctor. - Page 5 Do not use this device under direct sunlight or near to heating equipment, otherwise the temperature of the output will increase. To avoid electrical shock, disconnect the power cord before cleaning. Do not immerse the device in any fluids. Contact your health care professional if symptoms of sleep apnea recur. Check power cable and accessories regularly.
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Page 6: Product Model
Take preventive measures to avoid device damage due to water. Only distilled or pure water should be used in the water tank. Other liquids may damage the humidifier and device, or even endanger the user. Do not exceed the maximum water level marked on the water tank. Do not splash water into the device when installing the water tank. -
Page 7: Package Accessories
3. Package Accessories Item Articles Qty. Remark Host Standard Humidifier Standard Tubing Standard Mask Standard Adapter Standard User Manual Standard Air Filter Standard SpO2 Kit Optional Carrying Case Standard TF Card Standard 4. Device Components Dial Can be rotated clockwise or counterclockwise and pressed. -
Page 8: Device Symbols
TF Card port For placing TF card Power Port Connecting with the adapter Do not remove the Dial cap. The metal rod in the Dial may contact an external current source, causing damage to the host. If the Dial cap falls off, you may contact the dealer or the manufacturer to purchase a new Dial cap. -
Page 9: Start Running
6.1.5 Connect the power adapter with the power port on the back side of the device 6.1.6 Connect the power supply, then the device will show the main interface 6.1.7 Connect the power supply, press the on/off button, the device will start working. -
Page 10: Humidifier
7. Humidifier In some dry areas, long time use of the device at night may cause discomfort of the nose. This device has a humidifier and by adding water to the humidifier, moisture will be added to the inhaled air to prevent dryness of the nose. 7.1 Humidifier Composition Fig.7-1 Air Outlet... -
Page 11: Spo2 Kit
Fig.7-4 Press the Humidifier Separation Key, and pull the humidifier in the opposite horizontal direction from the host at the same time. 7.2.3 Adding water (1) Take off the humidifier cap: move the humidifier cap key to the right side, open the humidifier cap and take out the water tank by catching its inner part with your thumb and index finger like the picture below. -
Page 12: Parameter Settings
port. Attach the Oxygen probe’s sensor to the patient's index finger or any other finger. The sampling frequency of the SpO2 signal is 50Hz, and the update frequency of the device is 1Hz. The value of SpO2 is calculated by the average of the former eight pulse waveforms. - Page 13 TF card inserted Working Ramp has been set. Humidifier has been set Indicating the parameters setting interface is locked (when the power is connected, it is locked by default. Move the cursor onto the parameter icon, press the Dial and hold for 5 seconds to unlock it).
- Page 14 Fig.9-4 Selected status Fig.9-5 Parameter setting interface.2 Fig.9-6 Parameter setting interface.3 Setup Working Parameter Description Model range mode When the Auto ON setting is “ON”, if CPAP, S, T, user wears the mask and takes 3 breaths Auto ON ON/OFF S/T, APCV, under the standby state, then the device...
- Page 15 working state, then within 15 seconds AutoB the device will enter into the standby state. When this function is ON, the device will automatically enter into the standby state in case the mask or tubing falls off during sleep. CPAP: provides a constant level of pressure throughout the breathing cycle.
- Page 16 4-27 B-30F AutoB cmH2O Setting the Belex function, the device will automatically detect respiratory *Belex 0-3 level CPAP rhythm of the user and lower pressure to Models increase comfort for user. 4-20 B-20S cmH2O Inspiratory Positive Airway Pressure. B-25S, 4-25cm Maximum inspiratory pressure varies on B-25A, S/T,...
- Page 17 B-30T, B-30P, B-30F B-25T, B-25P, device works with InspTime 0.5-4.0s B-30T, T, S/T inspiratory time. B-30P, B-30F When the user triggers the inspiration, S, S/T, APCV, 0.5-4.0s the device outputs the IPAP for up to the InspTime Models AutoB maximum time. (Max inspiratory time) When the user triggers the inspiration, the device outputs the inspiratory S, S/T, APCV,...
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Page 18: System Setting Interface
9.4 System setting interface Rotate the "Dial" button to position the cursor on the main interface "System" and press the "Dial" button to enter the system set up interface shown in Fig.9-7. Fig.9-7 System setting interface 1 Fig.9-8 System setting interface 2 Fig.9-9 System settings interface.3... - Page 19 Parameter Setup range Description The device’s internal time can be set, and according to this time Time h-m-s the applied information for users will be recorded. It should be checked frequently to ensure the accuracy of the device’s time. The device’s internal date can be set, and according to this date Date yyyy-mm-dd the applied information for users will be recorded.
- Page 20 Fig.9-12 CPAP Information setting interface.1 Parameter Setup range Description 1/7/30/90/180/3 The calculation cycle of the device for the following UseCycle information items. Unit is "day". The time duration of the device being connected to the UseTime ------ power supply and it starting to run within the life cycle. Unit is “hour”.
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Page 21: Prompt
Fig.9-13 Alarm interface 10. Prompt Prompt Description Message The power supply is disconnected when the device in the working state, it will POWER provide a sound prompt via the buzzer, the duration time is more than or equal to 30 FAILURE seconds, during the prompt, pressing the "on/off ", or re-powering will stop the sound prompts. -
Page 22: Cleaning, Disinfection And Maintenance
11. Cleaning, Disinfection and Maintenance 11.1 Timing Based on hygienic reasons, under normal usage, it is recommended that the operator or user service and / or replace the parts as shown below: ●Clean the device, tube and filter before the first time use. ●Empty the water tank and clean it every day to prevent bacterial growth. -
Page 23: Troubleshooting
service life. Therefore, you should follow the suggestions given by the sanitizer supplier on the applicable specific material and application instruction. Lastly, use water to completely clean the components which have had close contact with the patient, such as mask, headgear and tube, etc., to prevent skin and respiratory tract infection caused by residual solution. - Page 24 tube. The device outputs a pretty high pressure Pressure sampling tube is blocked Dry the pressure sampling tube without any artificially or there is some water in it. or removing the block in it. high setting. The pressure sampling tube isn’t Connect the pressure sampling The pressure fluctuating connected with host.
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Page 25: Specifications
13. Specifications 13.1 Environmental Parameters Operating Storage 5℃ to 35℃ (41˚F to 95˚F) -20℃ to 55℃(-13˚F to 158˚F) Temperature Humidity 15% to 93% (no condensation) 15% to 93% (no condensation) Atmospheric 700 to 1060 hPa 700 to 1060 hPa Pressure 13.2 Physical Dimensions 255mm*200mm*112mm... -
Page 26: Maximum Flow
≤ 2cmH ± 0.5cmH 13.6 Maximum Flow According to the maximum flow of ISO 80601-2-70:2015 Standard CPAP Test pressure (cmH Average flow at the patient connection port (l/min) BIPAP Test pressure (cmH2O) Average flow at the patient connection port (l/min) Note: all test data were carried out under conditions with the humidifier and 22mm tube. -
Page 27: Pneumatic Diagram
13.13 Pneumatic Diagram 14. Traveling with the Device 1.Use the Beyond carrying case to carry the device and accessories along with you. Do not put them in your checked baggage. 2.This device operates on power supplies of 100 ～ 240 V and 50 / 60 Hz, and is suitable for use in any country in the world. -
Page 28: Disposal
list of components for certain purposes such as maintenance or connection to other equipment. Beyond will provide the circuit diagram and / or other technical documents in whole or in part according to your needs. 17. Disposal When the device reaches the end of its service life, dispose of the device and packaging in accordance with local laws and regulations. -
Page 29: Emc Requirements
19. EMC Requirements Guidance and manufacturer's declaration - electromagnetic emissions– this device is intended for use in the electromagnetic environment specified below. The user of the device should ensure that it is used in such an environment. Emissions test Compliance Electromagnetic environment-guidance The device uses RF energy only for its internal RF emissions... - Page 30 Guidance and manufacturer's declaration - electromagnetic immunity – this device is intended for use in the electromagnetic environment specified below. The user of the device should make sure that it is used in such an environment. IEC60601 Compliance Immunity test Electromagnetic environment-guidance test level level...
- Page 31 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.
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