BMC G2S B20A User Manual Download Page 1

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User Manual

Respiratory Insufficiency Ventilator and
Accessories

BPAP System

G2S BPAP Series

Summary of Contents for G2S B20A

Page 1: ...User Manual Respiratory Insufficiency Ventilator and Accessories BPAP System G2S BPAP Series...

Page 2: ...Using Oxygen with the Device 16 11 7 Inserting the SD Card Only for the device that equipped with SD card 17 11 8 Using the Optional Kits 18 11 9 Starting Treatment 18 12 Routine Use 19 12 1 Connectin...

Page 3: ...ming Information and Description 29 15 6 Reposition of Alarming 32 15 7 Alarming Journal 32 16 Cleaning and Disinfection 32 16 1 Cleaning the Mask and Headgear 33 16 2 Cleaning the Optional Kits 33 16...

Page 4: ...and SpO2 probe Class II Double Insulated For indoor use only AC Power DC Power IP22 12 5 mm Diameter Dripping 15 tilted There are high pressure be careful of electric shock Hot Surface Serial Number...

Page 5: ...Outlet WEEE Marking Logo of BMC Medical Co Ltd 2 Warning Caution and Important Tip WARNING Indicate the possibility of injury to the user or operator CAUTION Indicate the possibility of damage to the...

Page 6: ...ipment such as CT scanners Diathermy RFID and electromagnetic security systems metal detectors as it may cause unacceptable risk to the patient or damage to the device Some electromagnetic sources may...

Page 7: ...ment Dryness of the mouth nose and throat Abdominal bloating Ear or sinus discomfort Eye irritation Skin irritation due to the use of a mask Chest discomfort IMPORTANT TIPS An irregular sleep schedule...

Page 8: ...gree of Protection against Electric Shock Type BF Applied Part Degree of Protection against Ingress of Water IP22 Pressure Range IPAP 4 0 20 0 hPa only applies to G2S B20A G2S B20S G2S B20T 4 0 25 0 h...

Page 9: ...n Port hPa 3 9 14 19 24 Average Flow at the Patient Connection Port L min 90 150 150 145 110 When the working pressure is set to the values listed in the table the average flow rate at the patient end...

Page 10: ...setted by home care provider While working in auto feature the device will automatically adjust the IPAP and EPAP if it detects a sleep apnea S A bi level mode which responds to both your inhalation a...

Page 11: ...ure iCode A feature that is intended to give access to compliance and therapy management information The iCode consists of six separate codes displayed in the Patient Menu each code is a sequence of n...

Page 12: ...ex A therapy feature that is enabled by your home care provider to provide pressure relief during exhalation Standby State The state of the device when power is applied but the airflow is turned off m...

Page 13: ...0 G2S B20T Main device 2 4 inch TFT CPAP S S T T 20 G2S B25S Main device 3 5 inch TFT CPAP S 25 G2S B25A Main device 3 5 inch TFT CPAP S AutoS 25 G2S B25T Main device 3 5 inch TFT CPAP S S T T 25 G2S...

Page 14: ...ider for additional information on the available accessories of this device When using optional accessories always follow the instructions enclosed with the accessories The tube with a diameter of 15...

Page 15: ...s the humidifier is turned off Mute Button Press this button to mute the alert However if the problem causing the alert is not solved the alert will sound again two minutes later Knob Start treatment...

Page 16: ...d temperatures allow it to adjust to room temperature approximately 2 hours before beginning setup Make sure the device is away from any heating or cooling equipment e g forced air vents radiators air...

Page 17: ...other end of the power cord into the power outlet Fig 11 3 Note The length of the power cord and power adapter is 1 5 m and 1 8 m respectively without the function of preventing electromagnetic inter...

Page 18: ...Power Cord Locker 1 Assemble the power cord locker to the device directed by the positioning groove Fig 11 4 2 Open the power cord locker plug the power cord to the power supply and press the locker d...

Page 19: ...overing both your mouth and nose the mask must be equipped with a safety entrainment valve In order to minimize the risk of CO2 rebreathing the patient should observe the following instructions It is...

Page 20: ...must be placed in line with the patient circuit between the device and the oxygen source The pressure valve helps prevent the backflow of oxygen from the patient circuit into the device when the unit...

Page 21: ...GPRS Kit KS CM01 SpO2 Kit and WL 200 Cellular Module which configured for the device When the power failure no special operation is required after restore power supply The device will continue to wor...

Page 22: ...ntion to the humidifier indicator lights when using the humidifier The indicator lights indicate the On Off state of the humidifier It is off when all indicator lights go out CAUTION Observe the water...

Page 23: ...y adding moisture and heat if applicable to the airflow 13 1 Filling the Water Chamber 13 1 1 Removing the Water Chamber Grab the water chamber and pull it out of the device as shown in the figure bel...

Page 24: ...r it is filled with water as shown in Fig 13 4 and return it to the device as shown in Fig 13 5 Fig 13 4 Fig 13 5 WARNING For safety purposes the device must be placed on a flat surface at a level low...

Page 25: ...ional to the humidity level If none of the indicator lights light up it means that the heated humidifier is turned off The temperature of the water in the water chamber maintains a constant set level...

Page 26: ...u 14 1 1 Accessing the Main Interface Connect the power cord and power adapter properly The screen displays the Main Interface shown in Fig 14 1 or the Main Interface shown in Fig 14 2 or the Main Int...

Page 27: ...in Interface the second icon indicates the Initial Setup Interface and the third icon indicates the iCode Interface As you turn the Knob the cursor switches among the three icons and the interface dis...

Page 28: ...creases indicating a higher humidity level As you turn the Knob counterclockwise the numbering decreases indicating a lower humidity level The Humidifier option is still displayed in yellow as shown i...

Page 29: ...Fig 14 11 Press the Knob the cursor jumps to the second icon on the left side of the screen The screen displays the Initial Setup Interface as shown in Fig 14 12 Fig 14 12 2 Returning to the Main Int...

Page 30: ...e Knob to discontinue treatment This will blow off the vapor left in the humidifier to avoid any damage to the device When this feature is set to Off which means it is disabled the airfolw stops deliv...

Page 31: ...instant response Intermediate Requires operator to make instant on time response Low Requires operator to be more cautious about the change of the state of equipment 15 2 Visual Alarming The grading f...

Page 32: ...key is re pressed during the silence period the silence period will be re timed 15 5 Alarming Information and Description Alarm Message Alarm Priority Alarm Type Description Power Failure High Priori...

Page 33: ...ow Pressure Note The limens for different models Off 3 19 hPa applies to G2S B20T in 0 5 hPa increments the default setting is 4 hPa Off 3 24 hPa applies to G2S B25T G2S B25VT and G2S LAB in 0 5 hPa i...

Page 34: ...n increments the default setting is 1 L min Low Input Voltage Middle Priority Technology Alarm If the voltage supplied by power adaptor is lower than 22 V an audible alert will sound and the screen wi...

Page 35: ...e oeprators should examine the current alarming pre arrangement to check if it is applicable to each case of patient and such pre arrangement can only be changed by the professional doctors and must n...

Page 36: ...tructions in the user manual for the mask 16 2 Cleaning the Optional Kits For details refer to the cleaning instructions in the user manual for the corresponding user manual CAUTIONS It is recommended...

Page 37: ...clean water thoroughly 3 After cleaning air dry the tube in a cool well ventilated area and avoid direct sunlight It takes approximately 30 minutes to completely air dry the tube Check whether the tub...

Page 38: ...aging the skin or respiratory tract or causing allergies The device shall not be serviced or maintained while in use with a patient Sterilization of this device and its components other than recommend...

Page 39: ...u notice any unexplained changes in the performance of the device if it is making unusual or harsh sounds if it has been dropped or mishandled if the enclosure is broken or if water has entered the en...

Page 40: ...he patient sleeps with his or her mouth open and the pressurized air goes out via the mouth leading to nasal and throat dryness Use a chin strap to prevent the mouth from opening during sleep or use a...

Page 41: ...pressure is determined according to the patient s conditions and cannot treat sleep apnea if the treatment pressure is set too low It takes a maximum of four weeks to adapt to pressurized air Relax a...

Page 42: ...be holes in the mask or pressure sensing tube Contact your equipment supplier It is a faulty device Contact your equipment supplier The device produces very low pressures The air inlet of the device...

Page 43: ...with by other equipment even if that other equipment complies with CISPR EMISSION requirements Portable RF communications equipment including peripherals such as antenna cables and external antennas s...

Page 44: ...lectromagnetic environment specified below The user of the device should make sure that it is used in such an environment Immunity Test IEC 60601 Test Level Compliance Level Conducted RF IEC 61000 4 6...

Page 45: ...people 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 trans...

Page 46: ...EDICAL CO LTD DISCLAIMS ALL LIABILITY FOR ECONOMIC LOSS LOSS OF PROFITS OVERHEAD OR CONSEQUENTIAL DAMAGES WHICH MAY BE CLAIMED TO ARISE FROM ANY SALE OR USE OF THIS PRODUCT SOME STATES DO NOT ALLOW TH...

Page 47: ...390992...

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