background image

BT-720 Operation manual 

 

P/N:720-ENG-OPM-ENG-R03 

Bistos Co., Ltd.  

2020.10 

17 

5 SpO

2

 

5.1 Overview 

Blood oxygen saturation (SpO

2

) is the percentage of oxyhemoglobin (HbO2) capacity bound by oxygen 

in the blood in the total hemoglobin (Hb) capacity that can be combined, that is, the concentration of 

oxygen in the blood. 

The principle for monitoring the pulse SpO

2

 is to fix the probe fingerstall on the patient’s finger or toe, 

use the finger (or toe) as a transparent container for hemoglobin, use 660nm wavelength red light and 

950nm near-infrared light as the incident light, maximum output power is 300 mW, measure the light 

transmission intensity through the tissue bed, and calculate the concentration of hemoglobin and SpO

2

The passing lights depend on a variety of factors, most of which are constant. However, one of these 

factors, the arterial blood flow, changes with time, as it is pulsating. By measuring the light absorbed 

during pulsating, it is possible to obtain the arterial blood SpO

2

. Detection pulsation can give a 

“plethysmography” wave and pulse rate signal. 

The main screen displays “SpO

2

” value and “plethysmography” wave. 

This monitor applies to measure SpO

2

  of adults (>18 years) and pediatric  (<18 years,>30 days), 

neonate (<30 days).  Contact  SpO

2

  probe to Patient’s finger  (or toe)  to get “SpO

2

” value and 

“plethysmography” wave. 

SpO

2

 function of this monitor has been calibrated in factory. 

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

 

5.2 Safety information

 

  

WARNING

 

 

Please use SpO2 sensor supplied from Bistos, operate in accordance with the Manual, 

and observe all warnings and precautions. 

 

Before monitoring, check whether the sensor cable is normal. When SpO

2

 sensor cable is 

unplugged from the socket, the screen will display “SpO2 Sensor Off” error message, 

and trigger an audible and visual alarm simultaneously. 

 

If the sensor or sensor packaging has signs of damage, do not use this SpO

2

  sensor; 

return it to the manufacturer. 

 

If there is carboxyhemoglobin, methemoglobin or dye diluted chemical, the SpO

2

 value 

will have deviation. 

 

When the patient has a tendency to hypoxia, use the oximeter to analyze blood samples 

in order to fully grasp the patient's condition. 

 

Do not put the sensor on limbs with arterial duct or intravenous tube. 

 

Do not intertwine electrosurgical equipment cable with the sensor cable. 

 

Avoid using the monitor and sensors while using the NMR equipment, in order to avoid 

severe burns to the patient as a result of induced currents. 

 

During long time continuous monitoring of a patient, check the position of SpO

2

 sensor 

once every 2 hours, and move properly when the skin changes or every four hours. 

Some patients may require more frequent inspection, such as patients with perfusion 

disorders or sensitive skin, because persistent and prolonged monitoring may increase 

unpredictable skin changes, such as allergies, redness, blistering or pressure necrosis. 

 

Before using, verify compatibility between the monitor, probe and cable, otherwise it 

may cause injury to the patient. 

 

Functional testers cannot be used to evaluate the accuracy of pulse oximetry and pulse 

oximetry. 

 

SpO2 low alarm limit cannot be less than 85. 

 

NOTE

 

 

Do not put the oxygen probe and blood pressure cuff on the same limb, because blood 

flow occlusion during blood pressure measurement will affect the SpO

2

 readings. 

 

The monitor cannot be used to verify the accuracy of SpO

2

 probe and SpO

2

 equipment. 

Содержание BT-720

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

Страница 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...

Страница 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...

Страница 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...

Страница 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...

Страница 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...

Страница 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...

Страница 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...

Страница 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...

Страница 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...

Страница 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...

Страница 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...

Страница 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...

Страница 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...

Страница 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...

Страница 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...

Страница 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...

Страница 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...

Страница 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...

Страница 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...

Страница 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...

Страница 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...

Страница 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...

Страница 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...

Страница 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...

Страница 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...

Страница 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...

Страница 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...

Страница 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...

Страница 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...

Страница 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...

Страница 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...

Страница 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...

Страница 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...

Страница 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...

Страница 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...

Страница 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...

Страница 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...

Отзывы: