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BT-720 Operation manual 

 

P/N:720-ENG-OPM-ENG-R03 

Bistos Co., Ltd.  

2020.10 

20 

 

Produce first most clear signal - reflect SBP 

 

Oscillation amplitude reaches the peak - reflect MAP 

 

When the cuff pressure is suddenly lowered - reflect DBP 

Measuring mode: manual mode and automatic mode. Each mode shows systolic, mean and diastolic 

blood pressure. 

 

Manual mode  

Using Manual mode start to measures by hand 

 

Automatic mode measures  

Use manual mode to open automatic mode, then the measure will automatically turn to 

automatic mode after a certain time. During measurement, any error will stop the current 

automatic measurement, but not affect next automatic measurement unless the time interval 

less than 30s. If the time interval less than 30s, should delay the next automatic measurement, 

keep the interval more than 30s. 

The time interval can be choose In Automatic mode as 1, 2, 3, 4, 5, 10, 15, 30, 60, 90, 120, 180, 

240, 480 minutes. 

The monitor is defibrillation proof, so the monitor operates normally after defibrillation. 

 

6.2 Safety information

 

  

WARNING

 

 

Do not carry out non-invasive blood pressure measurement on patients with sickle cell 

disease and skin damage or any expected damage. Do not measure NIBP on traumatic 

body part. This may cause further injury. 

 

When pediatric and neonate patients are measured, in order to ensure the cuff pressure 

does not exceed its maximum measurement range of patient types (Adult mode: 

300mmHg and Pediatric mode: 240mmHg, Neonate mode: 150mmHg), you must ensure 

that you have selected the correct patient type (see patient information menu settings). 

Using the wrong type of pattern is likely to endanger the patient to patient safety, as 

higher blood pressure levels for adults does not apply to pediatric and neonate. 

 

For patients with severe coagulation disorder, determine if the automatic blood pressure 

measurement is carried out according to the clinical evaluation, since the friction of body 

and cuff may produce hematoma. 

 

Do not install a cuff on the limbs with intravenous infusion or duct, because it may lead 

to tissue damage around the duct when the cuff is inflated and makes the infusion slow 

down or be blocked. 

 

The inflatable tube connecting the blood pressure cuff and the monitor should be 

smooth without entanglement. The pressure generated by being kinked connection 

tubing may cause blood flow interference. 

 

For patients with severe thrombotic disorders, determine whether to carry out 

automatic blood pressure measurement according to the clinical situations, since the 

limb bundled with a cuff may produce hematoma. 

 

Measure blood pressure frequently will affect the distribution of blood flow, May 

endanger the safety of patients. 

 

Check the patient's physiological condition before measure blood pressure, in order to 

ensure that long time measure will not damage the circulation of patients 

 

For mastectomy patients, applying the NIBP cuff on the surgery side arm can cause 

lymphedema. Measure blood pressure on opposite side arm. 

 

Pressurization of the cuff can temporarily cause loss of function of simultaneously used 

monitoring device on the same limb. 

 

Measurement results may be affected by posture and mental state of the patient. 

 

If there are doubts on the measurement results, please use other blood pressure 

measurements and compare, if necessary, contact the Equipment Division. 

 

Summary of Contents for BT-720

Page 1: ...BT 720 Patient monitor Operation Manual Keep this manual for future reference P N 720 ENG OPM EUR R03...

Page 2: ...r no responsibility is assumed by Bistos for its use or any infringements of patents or other rights of third parties that may result from its use No license is granted by implication or otherwise und...

Page 3: ...ance 13 2 Preparing for operation 13 2 1 Installation 13 2 2 Connecting to power 14 3 Basic operations 14 3 1 Turn on 14 3 2 Turn off 15 4 Setup the monitor 15 5 SpO2 17 5 1 Overview 17 5 2 Safety inf...

Page 4: ...Accessories 29 13 Specifications 30 13 1 Safety specification 30 13 2 Hardware specifications 30 13 3 Functional specification 31 14 Common faults and maintenance 32 15 Manufacturer s declaration on...

Page 5: ...n this information thoroughly before using BT 720 IPX1 Indicates the protection level against the ingress of liquid IPX1 is protection against some water drops falling vertically It correspond the dev...

Page 6: ...if there is any visible sign of damage Only the DC power adapter supplied with the BT 720 is approved for use with the device Do not attempt to service the BT 720 patient monitor Only qualified servic...

Page 7: ...yed on the monitor are only for the doctor s reference and should not be directly used as the basis for clinical treatment This is not a therapeutic device For patients with pacemakers the cardio tach...

Page 8: ...accessories are about to exceed the useful life expected service life 5 years it must be treated in accordance with relevant local laws and regulations or the hospital s rules and regulations Do not c...

Page 9: ...ect such as a needle Do not hit with a hammer step on or throw or drop the battery Do not disassemble or modify the battery The battery can heat smoke deformation or burning When leakage or foul smell...

Page 10: ...pe of application This monitor is suitable for bedside monitoring of patient This monitor enables blood oxygen saturation SpO2 pulse rate PR and monitoring It is equipped with a replaceable built in b...

Page 11: ...astectomy Source 1 NHS Clinical Procedure_ Procedure for Blood Pressure Monitoring Wirral Community NHS Trust Dec 2013 2 Clinical Quality Patient Safety Unit QAS Clinical Practice Procedures Assessmen...

Page 12: ...Display the waveform and measured value 4 Alarm indicator Indicates the priority of physiological alarm and technical alarms in different colors and flashing frequencies High priority Red fast flashin...

Page 13: ...m will display the alarm message The system will shut down 3 seconds Figure1 4 Rear view Name Description 1 Network port For CMS 2 Type A USB For software upgrade 3 Type B USB Reserved for data transf...

Page 14: ...ipment standard Furthermore all configurations shall comply with valid version of IEC 60601 1 standard The personnel connecting additional devices to the input output signal ports are responsible for...

Page 15: ...ound the device When the device is moved from one environment to another the device may have condensation due to the differences in temperature or humidity In this case wait until the condensation dis...

Page 16: ...ing site of patient 3 1 4 Start monitoring Start monitoring in the following steps Check if the patient cable and the sensor are connected properly Check if the settings of the monitor are corrects su...

Page 17: ...the option as needed English The interface language of the monitor is English T rk e The interface language of the pulse oximeter is Turkish Espa ol The interface language of the pulse oximeter is Sp...

Page 18: ...nd precautions Before monitoring check whether the sensor cable is normal When SpO2 sensor cable is unplugged from the socket the screen will display SpO2 Sensor Off error message and trigger an audib...

Page 19: ...e monitor measured pulse rate Check the sensor mounting position whether the sensor is damaged or sensor type Reconnect the sensor or use new sensor 5 4 Setting SpO2 Select SpO2 parameter area to ente...

Page 20: ...If there is any other substance that absorbs the same wavelength the measurement may have false or low SpO2 values such as carbon hemoglobin methemoglobin methylene blue and indigo carmine SpO2 probe...

Page 21: ...Using the wrong type of pattern is likely to endanger the patient to patient safety as higher blood pressure levels for adults does not apply to pediatric and neonate For patients with severe coagula...

Page 22: ...the pressure measurement will not be reliable because the decrease of blood flow to the periphery would cause decrease in arterial pulsation Limit heart rate If the heart rate is below 40bpm beats min...

Page 23: ...Otherwise correct the measurement results with the following correction method If the cuff is above the heart level position increase 0 75mmHg 0 10kPa per centimeter of gap to the measured results If...

Page 24: ...9 Pediatric Range 10 164 Neonate Rang 10 104 Adult Pediatric Neonate default 50 40 20 Select DIA High Limit and enter value Adult Range 11 220 Pediatric Range 11 165 Neonate Rang 11 105 Adult Pediatri...

Page 25: ...fiber to clean this accessory because they will stick on the cuff and extension tube 6 6 2 Disinfection method 1 Sprinkle bleach solution Formula the proportion of water and bleaching powder to 1 10...

Page 26: ...y alarm prompt information the alarm state icon area displays the icon When a new physiological alarm or technical alarm occurs the alarm reset is automatically canceled Physiological alarm informatio...

Page 27: ...alarm Battery Low in this case connect the monitor to DC power and charge the battery 9 2 Battery usage guide Battery life depends on the frequency and time of use If the battery maintenance and stora...

Page 28: ...emble the battery throw it in fire or short circuit it Battery fire explosion and leakage may lead to personal injury Do not touch the leaking battery with naked hand directly 10 Caring and cleaning 1...

Page 29: ...for advice 10 3 Disinfection In order to avoid damage to the product we recommend that the product is disinfected only when it is deemed necessary by the hospital maintenance procedures We also recomm...

Page 30: ...safety according to IEC 60601 1 At least once every two years after replacing the power supply or the monitor falls down Check all monitoring or measuring functions not listed At least once every two...

Page 31: ...ernally powered equipment When you question the integrity of the external protective earthing or protective ground conductor parameter of the equipment the device must be powered by the internal power...

Page 32: ...kPa 70kPa 106kPa 13 3 Functional specifications 13 3 1 SpO2 SpO2 Standards compliant ISO 80601 2 61 2011 Display range 0 100 SpO2 display resolution 1 SaO2 accuracy 2 70 100 adult pediatric mode 3 70...

Page 33: ...mmHg Overpressure protection point hardware Adult 320 330mmHg Pediatric 265 275mmHg Neonate 160 165mmHg Static Pressure accuracy 3mmHg Electrical characteristics Supply voltage 10V 14V DC Maximum powe...

Page 34: ...NOTE Using unqualified accessories sensors and cables will increase the electromagnetic emission and reduce the electromagnetic immunity of the device Do not put the device close to other devices or...

Page 35: ...distance between portable and mobile RF communications equipment transmitters and the BT 720 as recommended below according to the maximum output power of the communications equipment Rated maximum ou...

Page 36: ...4 5 2006 1 kV differential mode 2 kV common mode 1 kV differential mode 2 kV common mode Mains power quality should be that of a typical commercial or hospital environment Voltage dips short interrupt...

Page 37: ...transmitters as deter mined 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...

Page 38: ...through strict quality control and inspection Compensation standard concerning repair replacement refund of the product complies with Framework Act on Consumers noticed by Fair Trade Commission of Re...

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