bionics patient monitor series operation manual bionics patient monitor series operation manual ....
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Head Office/Factory 687-5, Sangoan-ri, Hongcheon-eup, Hongcheon-gun,Gangwon-do, Korea (zip.250-804)Tel : +82-33-434-9041 Fax : +82-33-434-9043
Seoul Office/R&D1406, Masters Tower, 553, Dohwa-dong, Mapo-gu,Seoul, Korea (zip.121-748)Tel : +82-2-714-2960∼2 Fax : +82-2-714-2963
Customer Service Dept.Tel : +82-2-714-2962 Fax : +82-2-714-2963
Address of Region Representative ET MEDICAL DEVICES SPAVIA DE ZINIS 6, 38011 CAVARENO (TN) ITALY Tel : +39 0463 85 01 25 Fax : +39 0463 85 00 88
BIONICS Patient Monitor SeriesOperation Manual
www.ebionics.co.kr
OPERATION MANUAL
Guardian(BPM-770)Patient Monitor (Ver 1.0)
(JUL. 29. 2010)
Before using the product 3
Contacts 3
Product Guarantee 4
Symbols in the Manual 5
Precautions for use 6
Precations for Electrical Safety 10
Characteristics and Principles of Guardian 11
Composition of Guardian 12
How to set Guardian 13
Precations for Settings 13
Checkpoints Before Use 13
Maintenance and Cleaning After Use 15
Components of Guardian 16
Front & Operation Panel 16
Right side 17
Left side 18
Back side 19
Description of Product Symbols 20
Initial Screen 21
How to Use Guardian 24
How to Use 24
Alarms 25
Trends 27
Setup Setting 29
Default Setting 31
Printer setup(Optional) 32
Power & Battery Specifications 34
AC Power 34
Battery Specifications 34
Table of Contents
ECG Me asurement 36
How to Connect ECG Cable 36
Change of ECG Lead 37
Arrhythmia setting 37
ST SEGMENT setting 39
Respiration Measurement 41
How to measure Respiration 41
Change of Respiratory Mode 42
Blood Pressure Measurement 43
How to Measure Blood Pressure 43
Change of NBIP Mode 44
SpO2 Measurement 45
How to Measure SpO2 45
Change the SpO2 Mode 47
Body Temperature Measurement 48
How to Measure Body Temperature 48
Change of Temp Mode 48
Press Measurement (Optional) 50
Press Setting 50
Change of IBP Mode 55
EtCO2 Measurement (Optional) 57
CO2 Gas Measurement 57
Sidestream CO2 57
CO2 Calibration 59
Before Requesting After - Sale Service 60
Product Specifications 63
Product Warranty 69
Before Using the Product / Contacts 3
Guardian Series
Thank you for purchasing Guardian
For safe and efficient operation, please read the manual to learn about the functions of the
product before use.
Please keep this manual nearby to assist you with operating the functions of the product.
The product should be used under the supervision of a medical- related certified professional.
The product is used for examining patient’s abnormal condition. For the safety of the patient, only
the components or the accessories recommended by our company should be used.
If you connect any accessories to the product that is not specified in the manual, please be sure to
notify our company or an agency authorized to distribute our products.
Before Using the Product
For various services and product information, please feel free to contact our salesperson at the
following number.
For any questions about use or setup of the product, please contact the following number.
Technical Support: BIONICS Co., Ltd. Tel: +82-2-714-2962
※ For reporting defects or abnormalities, please note the model name, product serial number,
purchasing date, and abnormal points before contacting us.
Contacts
Patient Monitor
4 Product Guarantee Symbols in the Manual 5
Guardian Series
The product you have purchased comes with a 20 month warranty from the purchasing date or
a 2 year warranty from production date covering defective materials. For the accessories such
as the battery, external cables, sensors, pressure cuff, hose, the warranty for them is given for 6
months from the purchasing date.
We are not responsible for any physical, financial and mental loss or damage and direct or
indirect expenses caused by, or resultant from, accidental or special circumstances during the
use of the product. The warranty is limited to the repair or exchange of the product by the
authority of the company or the agency, for problems in materials or the manufacturing process
which occurred during use under normal circumstances.
The company has no legal responsibility for the confirmation of services, declarations or whole
warranty beyond the warranty specified above, which were supplied or will be supplied by the
agency or the staff of the company at their own discretion. The user cannot request the
company of services, declarations or whole warranty which were supplied or will be supplied
by the agency or the staff of the company at their own discretion based on the statements above.
The contents of this warranty represent all other warranties indicated or implied, and also
represent all kinds of service- related responsibilities of the product sellers for the product they
sell.
The product was manufactured under strict quality controls and the inspection process of the
company. The indemnification standard for product repair and exchange is according to the
Economic Planning Board notification “Regulation for the indemnification of consumer
damage”
Product Guarantee
Some symbols are used in this manual to help users or patients use this product safely and
appropriately and to prevent any risk to patients or damage to materials. Please read and
understand all warnings and precautions.
Each symbols mean :
Symbols in the Manual
The “Note” symbol is used to inform you of important, but not dangerous,information regarding installation, use, and maintenance of the product.
Use of this product is prohibited during MRI photographing. A fire may breakoutfrom the induced current, and the accuracy of the product and the MRI may beinfluenced by mutual interference.
All cables should be set properly. Cables and hoses etc. should be kept away fromthe patient, so that there is no possibility of the patient’s neck being entangled inthem, and the cables and lines should be well arranged for the safety of the staff inthe hospital.
The computerized ECG analysis should be judged by qualified medicalprofessionals, and it should not be the sole basis in determining necessity oftreatment for the patient.
NOTE
The “Caution” symbol indicates that a situation may occur resulting ininjury or damage to the patient, though not life-threatening, when thecaution is ignored.
CAUTION
The “Warning” symbol indicates that a dangerous situation may occurresulting in fatal injury or death of the patient, or may incur material andfinancial damage when the warning is ignored.
WARNING
WARNING
Patient Monitor
6 Precautions for Use Precautions for Use 7
Guardian Series
Precautions for Use
Do not operate or store the equipment under the following environments.
Avoid the damp locations, and do not operate the equipment withwet hands.
Locations where the temperaturefluctuation is rather big.(Operational temperature range:10~45。C, Moisture level : 30~85%)
Locations where moisture levelcould go up considerably or whereair is not ventilated properly.
Locations where sudden impactor vibration could be received.
Locations close to electricalheating apparatuses.
Locations where exposed todirect sunlight.
Locations exposed to chemicalor explosive gas.
Disassembling of Product should bedone only by the authorizedpersonnel, otherwise we will not beobliged to provide any services at all.
When pulling out the power cord,be sure to grab the plug and pull,out, not the cord.
Do not plug in the power, until theinstallation is completed, otherwise,it can cause a damage to theProduct.
Make sure to prevent dust and especially metal debris, from penetrating in.
Standard operational conditions are as follows.- Temperature : 10℃ ~ 45℃ (50 ~ 113℉)- Altitude : 70 ~ 106Kpa- Humidity : 30 ~ 85%
Standard storage and transportation conditions are as follows.- Temperature : -10℃ ~ 50℃ (14 ~ 122℉)- Altitude : 70 ~ 106Kpa- Humidity : 20 ~ 95%
Patient Monitor
8 Precautions for Use Precautions for Use 9
Guardian Series
Leakage, heating, ignition or rupture of the battery may cause fire or injury.
- Do not use batteries beyond those specified in this manual.
- Do not short-circuit the battery and do not heat, disassemble, or dispose of it in a fire.
- Do not mix using the used battery with new batteries , different kind of batteries,
other company batteries
- Do not insert batteries with (+) and (-) ends reversed.
When the product is not used for a long time, separate the battery from the
product.
When the product has been moved, make sure to turn it off and arrange the
accessories in order. Injured cords or cables may cause fire or electric shock.
CAUTION
In order to obtain the best results, theses instructions for use are especially
important when applying the specified sensors, and all warnings and cautions
should be obeyed. If the sensors are exposed to excess natural light, we
recommend that you cover the sensors with an opaque material. Excessive light
from operating lamps (especially xenon gas lamps), bilirubin (red-yellow) lamps,
fluorescent lamps and direct sunlight may influence the measurement results.
If results are not available at all or are inaccurate, please check the following:
- If the patient has poor blood flow, attach the sensors to other fingers or toes.
- Check if the sensor is properly placed.
- When the electric operation equipment is used, make sure the sensors are not
positioned close to the cables.
- The Sensor-attached site should be kept clean and not oily. Clean the sensor and
skin if necessary.
NOTE
Interpretation of the measurement value of arterial blood pressure should be
performed by medical professionals.
Arterial blood pressure may be influenced by the patient’s posture, physical
condition and other factors such as a patient’s movement.
The product may not work well when it is kept or operated beyond the
temperature and humidity specified.
Since the use of the inappropriate sensors such as a sensor that is too tightly
wrapped with adhesive tape or use of additional adhesive tape, lack of a periodical
check, or inappropriate setting of sensors may lead to skin injuries and inaccurate
measurement results. The user should read the manual and the precautions
carefully before use.
Premature neonates and patients with chronic pulmonary disease should be
checked for oxygenation levels before starting treatment.
Sensor-attached sites should be checked at least every 8 hours(every 4 hours for
reusable finger sensors on adults). Please check if the sensors are properly
attached, if the skin condition is normal, and if the sensors are well positioned.
Nail polish or calluses may obstruct measurement. Special care is required for
patients with poor blood flow. If the sensor attachment status is not checked
periodically, it may lead to skin injury by extended contact and necrosis from the
pressure. Patients with weak blood flow should be checked every 2 hours
If you want to turn off the Guardian while you’re operating, please use the power
switch where is the front of the product.
CAUTION
Patient Monitor
10 Precautions for Electric Safety Characteristics and Principles of Guardian 11
Guardian Series
Precautions for Electric Safety
Please check the following points before use.
Is the product supplied with the appropriate power? (100~240VAC)
Are all connecting parts (power cables or the product) properly connected?
Is the product completely grounded? (If not, noise may occur.)
Before turning the power on, is the accessory for measuring the target parameter well connected
to the product?
Characteristics and Principles of Guardian
Guardian is Patient-monitoring equipment. Guardian measures the patient’s ECG, blood pressure
(invasive and noninvasive at two points), end-tidal partial pressure respiration (EtCO2), body
temperature (Temp), oxygen saturation of arterial blood and pulse (SpO2). Information on the
patient’s condition is displayed as numeric values and waveforms.
Guardian provides a variety of information about the patient. The user can choose the functions
they want to use. The vital sign information provided by the product includes ECG, heart rate,
respiratory rate based on respiration, maximum, minimum and mean blood pressure by invasive
and noninvasive methods and percentage of blood oxygen concentration measured by the changes
during a pulse cycle of arterial blood, pulse, and temperature.
The patient’s vital signs and condition are displayed on an LCD screen in realtime. The user can
set alarms or adjust the setting values using the buttons on the front. Guardian provides the basic
vital sign information of the patient to the user.
To prevent electric noise during use, the product should be installed apart from
dynamo, X-ray equipment, broadcast equipment or portable cables. An inaccurate
result may occur when these equipment are placed near the product. Guardian
requires an independent power circuit and a stable earth connection. Sharing power
with other electric equipment may result in inexact results.
NOTE
Guardian classified as follows :
It is a Class I equipment with defibrillation proof, Type CF grade for ECG, Resp,
IBP and BF grade for EtCO2, SpO2, NIBP and Temp.
Please do not use this product near inflammable anesthetics and diluents.
The noise level is “B” Class according to the IEC/EN 60601-1 (Safety of Electric
Medical Product), and the noise redemption is “B” Level according to the IEC/EN
60601-1-2 (Electromagnetic Compatibility Requirements)
Protection grade against water is “IPX 0”
NOTE
Patient Monitor
12 Composition of Guardian How to Set Guardian 13
Guardian Series
Composition of Guardian (Accessories) How to Set Guardian
Standard Accessories
Optional
- ECG Cable 3 lead type - TROLLEY (Rolling Cart)
- SpO2 extension Cable - Wall Mount
- DISPOSABLE SpO2 SENSOR - Neonate Cuff
- Clip Type SpO2 sensor (Y-type) - Child Cuff
- Printer Module - Press Measuring Kit (IBP Kit)
- EtCO2 Kit set - Skin Temp. probe
- Electrode (50 PCS / 1SET) - Roll Paper
Main 1 setECG Cable
5 Lead Type (1EA)
SpO2 Finger Probe
(1EA)
Electrode
(5PCS/1set)
NIBP Hose (1EA) Adult Cuff (1EA)
Body Temperature
Sensor(For Rectal use)
(1EA)
Power Cord
Adapter(1EA)
15V 3Ah
Operation Manual
(1EA)
(1) Precautions for Settings
Pay attention when setting Guardian for the following points
- Use Guardian under conditions of 10℃ ~ 45℃ of circumstantial temperature and 30% ~ 85%
humidity.
- Check the connection status of the power cord.
- Do not connect multiple cords to the power supply.
- Place the main body on a flat area.
- If noise occurs, ground the equipment.
- Do not use any electric cords generating connecting noise.
- Take care since the product can be broken by mechanical shock.
- Get rid of dust or inflammable material near the product when setting it up.
(2) Checkpoints before Use
Check the following points before measuring the patient’s condition.
- Make sure there is no mechanical risk.
- Check the lead, power plug, and accessories connected on the outside.
Precautions Before Use ECG
① Do not use product near dynamo, X-ray equipment, broadcast equipment.
② Use disposable electrodes.
③ Do not twist the cable.
④ Attach each Lead properly.
⑤ Keep the patient motionless with comfortable position while measuring.
⑥ Sterilize Lead periodically.
Precautions Before Use SpO2
Patient Monitor
14 How to Set Guardian How to Set Guardian 15
Guardian Series
① Do not use product near dynamo, X-ray equipment, broadcast equipment.
② Keep the patient motionless with comfortable position while measuring.
③ Sterilize sensor periodically.
Precautions Before Use Temp
① Do not use product near dynamo, X-ray equipment, broadcast equipment.
② Sterilize sensor periodically.
③ Use disposable hygiene cover.
Precautions Before Use NIBP
① Do not use product near dynamo, X-ray equipment, broadcast equipment.
② Do not twist hose
③ Keep the patient motionless with comfortable position while measuring.
Precautions Before Use IBP
① Do not use product near dynamo, X-ray equipment, broadcast equipment.
② Keep the patient motionless with comfortable position while measuring.
③ Do not twist cable
Precautions Before Use EtCO2
① Do not use product near dynamo, X-ray equipment, broadcast equipment.
② Keep the patient motionless with comfortable position while measuring
③ Do not twist cable
(3) Maintenance and Cleaning After Use
A. Keep the product cleans by cleaning it using a soft cloth at least once a month. Do not use
thinner, ethylene, oxidant or lacquer since these may damage the product.
B. Keep the accessories clean of dust or foreign materials. For cleaning, use a soft cloth and
clinical alcohol.
C. Do not soak the accessories in liquid or detergents. Keep the product and accessories out of any
liquid.
Maintenance and Cleaning after using ECG
① Sterilize Lead periodically after using
② Discard the disposable electrodes in designated locations.
③ Store the cable without twisting.
Maintenance and Cleaning after using SpO2
① Sterilize the Probe periodically after using.
② Store the cable without twisting.
Maintenance and Cleaning after using Temp
① Sterilize the Probe periodically after using.
② Discard the disposable covers in designated locations.
③ Store the cable without twisting.
Patient Monitor
16 Components of Guardian Components of Guardian 17
Guardian Series
Components of Guardian
(1) Front & Operation Panel
① AC Power LED ⑦ NIBP START/STOP Button
② Battery LED ⑧ PRINT START Button
③ Power Button ⑨ EXIT Button
④ ALARM ON/OFF Button ⑩ MENU Button
⑤ SCREEN Button ⑪ ALARM STATUS LED
⑥ FREEZE Button
① PRINT FEED Button ③ PRINT POWER LED
② PRINT ERROR LED
(2) Right Side
① ①⑪
②
②
③
③
④ ⑤ ⑥ ⑦ ⑧ ⑨ ⑩
Patient Monitor
18 Components of Guardian Components of Guardian 19
Guardian Series
(3) Left Side
① ECG/RESP Connection Terminal ④ SpO2 Connection Terminal
② IBP Connection Terminal (Option) ⑤ NIBP Connection Terminal
③ TEMP Connection Terminal ⑥ CO2 Connection Terminal (Option)
①
④
⑤
⑥
②
③
(4) Back Side
① PORTABLE HANDLE ⑤ Alarm Connection terminal
② ID LABEL / Battery Cover ⑥ LAN PORT
③ Grounding Port ⑦ RS-232 PORT
④ DC IN ⑧ VGA PORT
①
④ ⑤ ⑥ ⑦ ⑧
②
③
Patient Monitor
20 Description of Product Symbols Description of Product Symbols 21
Guardian Series
Composition of Guardian (Accessories)
Icon Comments Icon Comments
Type CF Product,Defibrillation protected Alarm On/Off
Type BF Product,Defibrillation protected
Screen Change(Screen)
Stop Waveforms(Freeze)
Non Invasive BloodPressure Manual
Measurement (NIBP)
Start Printing (Printer)
Initial Screen (Exit)
Signal Input
Temperature
Oxygen Saturation
Use for ProgramUpgrade
Screen Transfer
Power stand-by switch
Attention, consultaccompanying documents
Ground
SYSTEM PowerOn/Off
Signal Output
Invasive BloodPressureIBP
ECG/RESP
NIBP
LAN Port
TEMP
SpO2
RS-232CPort
VGA Port
Electrocardiograph /Respiration
Non Invasive BloodPressure
Use for CentralMonitoring
(1) Initial Screen
(Fig1. Main Screen)
① WAVE Area : Display the graph of patient’s vital sign and condition
② MINI TREND : Display the Trend information of patient
③ FiCO2(Fractional concentration of carbon dioxide in inspired gas) : Display the Fractional
concentration of carbon dioxide in inspired gas of patient.
④ RR, TEMP : Display the respiration and temperature value of patient
⑤ IBP : Display the Invasive Blood pressure of patient.
⑥ NIBP : Display the Non Invasive Blood Pressure of patient.
⑦ SpO2 : Display the Oxygen Saturation of Patient
⑧ HR : Display Heart Rate.
⑨ Time : Display the present time
⑩ Each Measurement Mode Icons : Display the measurement and Lead off etc.(Refer to next
page <Table 1 : Explanation of Screen Icons >)
⑪ Patient Information : Use to set the room and bed of patient.
①
④
⑤
⑥
⑦
⑧
⑪ ⑩ ⑨
②
③
Patient Monitor
22 Description of Product Symbols Description of Product Symbols 23
Guardian Series
(A) (B)
(D) (C)
Icon Meaning How to display
ECG Lead Fault & Lead off Flickers at 1-second interval
Arrhythmia Detect Flickers at 1-second interval
Pacemaker Detect Flickers at 1-second interval
No Finger & No Sensor Flickers at 1-second interval
On NIBP measuring Flickers at 1-second interval
NIBP measurement Error Flickers at 1-second interval
NIBP Over Pressure Flickers at 1-second interval
NIBP Auto pressurization Fixed. Fixed.
IBP1 Lead Fault Flickers at 1-second interval
Temp1 Lead Fault Flickers at 1-second interval
Alarm OFF Fixed when Alarm OFF is set.
Alarm Suspend: Automaticallycancelled after 2 minutes. Flickers at 1-second interval
Printing Flickers at 1-second interval
Waveform stop Flickers at 1-second interval
AC in use Fixed.
Battery in use Fixed.
(Table 1) Explanation of Screen Icons
Guardian provides 4 different screens to use “Screen” button.
4 screens are as follows.
A. Full Parameters Screen (Main Screen)
B. 1 (ECG Wave) and 6(ECG, SpO2, NIBP, RR, TEMP, CO2) Parameters Screen
C. 1 (ECG Wave) and ALARM Occurrence Information Screen
D. TREND Screen
NOTE
Patient Monitor
24 How to Use Guardian How to Use Guardian 25
Guardian Series
How to Use Guardian
(1) How to Use
Turn on the main power switch at the back of the product. Check the light-on
status of the AC LED in the front, and push the power switch 1~2 seconds to
turn it on.(If any problems occur, refer to the “How to solve the problems”
section in the manual )
If you want to change the setting value etc. during use, push the Menu button
to change the setting values per each measurement parameter
When the measurement sensor is connected to the patient, the information to
the patient is displayed as values and waveforms on the LCD screen.
Refer to the table below for the details of how to measure each parameter.
- ECG measurement Page 39
Page 44
Page 46
Page 48
Page 51
Page 52
Page 59
- Respiration measurement
- Blood pressure measurement
- SpO2 measurement
- Body temperature measurement
- IBP (Press) measurement(optional)
- EtCO2 measurement(optional)
Step 1
Step 2
Step 3
Step 4
(2) Alarms
Different alarms are provided in Guardian for the sake of the user’s convenience. Please read
carefully the contents of this section in order to learn how to interpret and react appropriately to
the alarms.
High Alarm
- The High alarm will sound when the measurement values exceed the proper range.
- In High alarm, 5 alerting sounds ring for 2 seconds, for a total of 10 times. After 8 seconds,
the alerting sounds are repeated.
Information Alarm
- The information alarm rings to notify you of any announcements or if there has been an error
measurement.
- The information alarm sounds like a chime bell, and rings at an interval of 5 seconds to alert
the user.
- The information alarm rings for the following situations:
a. If there is a failure in the NIBP measurement or overpressure.
b. At Lead fault or Lead off during measurement.
c. If the finger is not attached to the finger probe during measurement of SpO2.
d. If the battery is low.
- When the information alarm rings, it can be cancelled by operating the function switch or
Menu switch. (The Exit switch is recommended.)
The alarms in the product conform to the international standard “EN 475:1995”
- A High alarm and Information alarm were adopted in Guardian
We recommend that you listen to the alarms before using the product.
NOTE
Push the Power button 1~2 seconds when turn it off and then “Power off”
massage will be displayed.
NOTE
Patient Monitor
26 How to Use Guardian How to Use Guardian 27
Guardian Series
How to set the alarm
To change the alarm setting, push the Menu button once to select “Alarm”
▶ Alarm Range
Step 1
Parameter
ECG [bpm]
SpO2 [%]
Systolic
Diastolic
Mean
Systolic
Diastolic
Mean
IBP[mmHg]
NIBP[mmHg]
Setting rangeHIGH LOW
10 ~ 300, OFF
21 ~ 99, OFF
40 ~ 295, OFF
30 ~ 285, OFF
35 ~ 290, OFF
5 ~ 149, OFF
40 ~ 295, OFF
30 ~ 285, OFF
35 ~ 290, OFF
20℃ ~ 49℃, OFF
2% ~ 99%, OFF
OFF, 5 ~ 295
OFF, 20 ~ 98
OFF, 30 ~ 290
OFF, 25 ~ 280
OFF, 30 ~ 285
OFF, 1 ~ 145
OFF, 30 ~ 290
OFF, 25 ~ 280
OFF, 30 ~ 285
OFF, 10℃ ~ 40℃
OFF, 1% ~ 98%
RESP [rpm]
TEMP [℃]
EtCO2 [%]
(3) Trends
To check the Trend date for the
patient being measured, push the
Screen button three times
1. The saved Trend Date can
bechecked using the Menu button
by moving it to the left or right.
2. Trend Date is saved from the right
to the left
For the sake of the user’s convenience, the function of Alarm On/Off functions
are added to each parameter. The state of Alarm On/Off does not affect the setting
values of the alarm.
NOTE
Guardian Trend Data provides 4320 data in total at an interval of 1minute for 72
hours.
NOTE
Patient Monitor
28 How to Use Guardian How to Use Guardian 29
Guardian Series
①
②
③
(Fig 2. Trend Screen)
① Parameter name for measurement
② Time of the storage
③ Standard bar
(4) SETUP Setting
The setting of the basic default value, print setting, volume adjustment and language selection
can be changed at the user’s convenience.
Setup is as follows.
To change the SETUP setting, push the Menu button once to select SETUP
▶ By operating as detailed above, you can change the setting of each SETUP menu.
Step 1
If you are moving the MENU button to the left or right fast, function of the
searching is going to be fast.
NOTE
Patient Monitor
30 How to Use Guardian How to Use Guardian 31
Guardian Series
Setup Menu
LEAD TYPE 3 LEAD/5 LEAD Select ECG Lead Cable
TRACEECG1,ECG2
SpO2,IBPRESP,EtCO2
Select Wave displayed on thescreen.
NUMERICSpO2
IBP,NIBPRR/TEMP,EtCO2
Select parameter displayed onthe screen.
TRAND TRACE/TIME Indicate TREND on first screen.
BED NUMBER 0~99 Input the BED number
PATIENT NAME Input the patient name
PATIENT
SOUND
Adult / Neonate
HR,ST LEVELSpO2
IBP,NIBPRESP/TEMP
EtCO2
Select the adult or neonate
Setup the existence of Soundwhen parameter alarm occurs
DATE / TIME
YEAR : 2000 ~ 2050MONTH : 1 ~ 12DATE : 1 ~ 31HOUR: 0 ~ 23
MINUTE : 0 ~ 59
Input the date/ time
LANGUAGE
ENGLISH ,SPANISHGERMAN, ITALIANFRANCE, CHINESEPOLISH,RUSSIAN
CZECH
Select the language
SOUND VOL.
PRINTER
0 ~ 7
Refer to Page 35 : Printer Settings
Set Beep Sound
Initialize
DEMO
EXECUTE
ON / OFF Setup the Demo
NETWORK
NURSECALL
Setup the Network
ON / OFF Setup the wire remote buzzer
Range of change Explanation
Parameter
ECG
Lead II II
Speed 12.5 mm/sec 12.5 mm/sec
Gain 10 mm/mV 10 mm/mV
Filter 1.0 ~ 40 Hz 1.0 ~ 40 Hz
HR > High Limit 150 bpm 200 bpm
HR < Low Limit 50 bpm 100 bpm
RESP
APNES Time OFF OFF
High Limit 30 rpm 100 rpm
Low Limit 5 rpm 30 rpm
Size 2.0 Ohm 2.0 Ohm
Speed 6.3 mm/sec 6.3 mm/sec
SpO2
High Limit OFF 95 %
Low Limit 90 % 80 %
Gain X 2 X 2
Speed 12.5 mm/sec 12.5 mm/sec
NIBP
NIBP Mode Manual Manual
Interval 60 60
High Alarm Limit 160/90(110) 90/60(70)
Low Alarm Limit 90/50(60) 40/OFF(OFF)
IBP
Label ABP ABP
Scale Optimum Optimum
Speed 12.5 mm/sec 12.5 mm/sec
High Alarm Limit 150/120(130) 90/60(70)
Low Alarm Limit 80/60(70) 55/OFF(35)
TEMPHigh Alarm Limit 39℃ 39℃
Low Alarm Limit 30℃ 36℃
EtCO2High Alarm Limit 45 45
Low Alarm Limit 10 10
Range of change Explanation Explanation
(5) Default setting
The default settings of the values can be used, without the need of changing the setting values of
each parameter.
Patient Monitor
32 Printer Setup (Optional) Printer Setup (Optional) 33
Guardian Series
Printer Setup (Optional)
The patient’s information can be printed out using the printer.
To change the printer setup, push Menu button to select SETUP
PRINTER
Step 1
▶ By operation as detailed above, you can select the function of the Printer mode.
Setting Mode
SYNC
MODE
SOURCE
SIZE
Alarm / Manual
Wave+Trend / Wave / Trend
ECG2/SpO2/IBP/RESP
120 ~ 300mm(To be adjusted at 15mm unit)
When “Alarm” is selected, the date is automaticallyprinted out if the data is out of range.
Print the waveform and Trend Data / waveform only /Trend Data only.
Select the waveform to be printed out (ECGwaveform is printed out as a basic factor.)
Select the length of printed paper.
Range of change Explanation
<Ex :Trend printing>
<Ex:Wave printing>
Do not print greater than consecutive 3 times
There is possibility of fire, Do not use printing for 5min. after consecutive 3 times
of printing
CAUTION
Patient Monitor
34 Power & Battery Specifications Power & Battery Specifications 35
Guardian Series
Power & Battery Specifications
Both AC and DC power is used for Guardian. Basically, AC power is used and a rechargeable
battery is available for portable use.
1. AC Power (110 ~ 240 VAC)If the AC power is connected to the main body of the product, a light-green color lights up on
the AC LED on the front. If the product is not being used, the power changes automatically to
the recharging mode.
Battery 상태 설 명
Battery full
After use for 50 ~ 60 minutes
Requiring recharging
Low Battery requiring recharging
2. Battery SpecificationsWhen the AC power is disconnected and the switch is turned on, the power is supplied using
the battery, signaled by the orange light on the battery LED.
A. Signs for Battery
B. Time for 1ea of battery
Recharging time : 9 Hours or more
Use time :120 Minutes
C. Natural lifetime for spontaneous discharge of battery
The table below shows the lifetime for spontaneous discharge of the battery when the product
is unused.
Storage temperature Life for spontaneous discharge
0℃ ~ 20℃
21℃ ~ 30℃
31℃ ~ 45℃
9 months
6 months
3 months
D. Type of Battery
The same sort of battery should be used for replacement.
- Model : 3S2P(LS18650)
- Type : LI-Ion Battery
- Manufacturer: BTS Power
E. Time for the Battery exchange
The lifetime of the battery gets shorter if it is not 100@ recharged for use
The battery is recharged when AC power is confirmed.
Charge / Discharge ration Number for use
100 % Charge / discharge
50 % Charge / discharge
30 % Charge / discharge
1200 times
500 times
200 times
During operation using AC power, noise may occur in the waveform. If this is the
case, ground the product soundly.
An AC power connection in a wet or damp area may cause electric shock or fatal
damage to the product.
There are more chance to get fire or heating to use printer constantly. Please do
not use 5 minutes after using 3 consecutive times.
CAUTION
When the battery is disconnected, all data (Trend, Setup values and time etc.) are
saved in the memory within Guardian for about 3 days. If the product is kept off
of the battery for more than 3 days, all the data may be deleted.
CAUTION
For the protection of the environment, please contact the agency you purchased
the product from when you wish to discard the battery.
Contact the agency you purchased battery in case battery should be changed.
CAUTION
Patient Monitor
36 ECG Measurement ECG Measurement 37
Guardian Series
ECG Measurement
(1) How to Connect the ECG Cable
Connect the ECG cable to the ECG/RESP connection terminal of themeasurement module.
Step 1
To change the printer setup, push Menu button to select SETUPStep 2
<If 5 leads are attached> <If 3 leads are attached >
Lead Color of electrode
RA (R)
LA (L)
LL (F)
RL (N)
V (C)
White
Black
Red
Green
Brown
Attaching site
Just below the clavicle (scapula) near the rightshoulder
Just below the clavicle (scapula) near the leftshoulder
Lower area of the left side of the abdomen
Lower area of the right side of the abdomen
Select the candidate lead for measurement amongthe chest leads
(2) Change of ECG Lead▶ To change the setting of the ECG Lead waveform, push the Menu button to obtain the
pull-down menu below.
(3) Arrhythmia SettingArrhythmia in ECG has the function which judges the abnormality of the heart cardiac
ventricle.
BIONICS diagnosis program A can detect the below 3 kinds of Arrhythmia which can be fatal
on patient’s life
With the use of an electric pacemaker, do not touch the patient, table, or other
equipment.
Check if the ECG cable is damaged before taking the ECG measurement. (A
damaged ECG cable cannot protect the patient.)
Do not use disposable electrodes. (They may cause noise.)
WARNING
Patient Monitor
38 ECG Measurement ECG Measurement 39
Guardian Series
Asystole (ASY)
Ventricular Tachycardia (V-TAC)
Ventricular Fibrillation (V-TAC/V-FIB)
BIONICS diagnosis program B can detect the below kinds of Arrhythmia except the above
mentioned 3 types
Asystole
Ventricular Tachycardia
Ventricular Bradycardia
Ventricular Fibrillation
PVC
R-on-T
Missed Beat
Tachycardia
Bradycardia
Bigeminy
Trigeminy
Couplet
(4) ST SEGMENTThe value of ST Level can fall or rise unusually in case myocardial infarction occurs . It is
clinically necessary to observe the value of ST Level in all of LEAD. BIONICS ST Level
program measures each value of ST Level of LEAD I and LEAD II. LEAD I is fixed for
Channel 1 and LEAD II is fixed for Channel 2. The unit for ST Level is mV and in ascending
case, it is expressed as + sign, in descending case, it is expressed as - sign.
1) ST Level Condition
2) ST Level program of Bionics gets the value of ST Level on the basis of -78ms(ISO)
and +109ms(ST) with R peak as the center
ST Point Range of Change
Datum point for ST Level measurement
ST Point
J Point + 0ms
J Point + 30ms
J Point + 40ms
J Point + 50ms
J Point + 60ms
J Point + 80ms
Arrhythmia diagnosis program is designed to detect the abnormality of the
ventricular. However, it may occur not to judge exactly the existence of
Arrhythmia. Therefore, in case Arrhythmia is detected, the judgment of the
clinical specialist is positively necessary
WARNING
In case of measurement Arrhythmia, it is principle to fix LEAD at LEAD II of the
channel 1.
WARNING
Patient Monitor
40 ECG Measurement Respiration Measurement 41
Guardian Series
▶ By operating as detailed above, you can select each function of the ECG mode.
Setting Mode Range of Change
LEAD
GAIN
SPEED
FILTER
AREA
ALARM
ST SEGMENT
ARRHYHMIA
PACEMAKER
LEAD I, II, III, aVR, aVL, aVF, V
5, 10, 15 mm/mV
6.3, 12.5, 25 mm/sec
0.5 ~ 40 Hz
0.5 ~ 80 Hz
0.05 ~ 40 Hz
0.05 ~ 80 Hz
1.0 ~ 40 Hz
5.0 ~ 20 Hz
50, 60 Hz
High (10 ~ 300bpm) range
Low (5 ~ 295bpm) range
Alarm ON/OFF
DIAGNOSIS ON/OFF
DIAGNOSIS ON/OFF
DIAGNOSIS ON/OFF
Explanation
Change the ECG Lead on screen
Set the size of ECG waveform
Set the speed of ECG waveform
Set the analog and digital filter
of the ECG waveform
If there is input, the eliminationfrequency is set.
Set the upper limit of HR
Set the lower limit of HR
Alarm operation / rest
LEVEL check / rest
Arrhythmia check / rest
Defibrillator check / rest
<Sites for 3 leads attachment> <Sites for 5 lead attachment>
Respiration Measurement
Changes in the chest impedance resulting from the patient’s respiration is measured and displayed
as a waveform and the values will appear on the screen.
(1) How to Connect the ECG Cable
Connect the ECG cable to the ECG/Res connection terminral of themeasurement module.
Step 1
Attach the electrodes for respiration measurement by referring to the figuresbelow.
Step 2
Respiration is measured with the ECG and HR etc., using the ECG cable.
Do not judge the patient’s condition only with the respiratory value and the
waveform.
NOTE
Patient Monitor
42 Respiration Measurement Blood Pressure Measurement 43
Guardian Series
Blood Pressure Measurement
(1) How to Measure Blood Pressure
(2) Change the Respiration Mode▶ To change the setting of respiratory waveform, push the Menu button to
select RESP.
▶ By operating as detailed above, you can select each function of the RESP mode.
Setting Mode Range for Change
SPEED
SIZE
TRACE
6.3, 12.5, 25 mm/sec
0.5, 1, 2, 4 OHM, OPTIMUM
ON / OFF
Explanation
Set the speed of RESP waveform
Set the size of RESP waveform
Set the display of waveform
Connect the gray hose to Guardian as shown below.Step 1
Wrapping the cuff to tight or too loose on the measuring site may cause errorsin the value.
Step 2
The Alarm setting for Apnea can be set up in ALAR → RESP → APNEA by
MUNE button
■ APNEA Alarm Range : OFF, 10 ~ 60 seconds (Adjustable by 1 sec. unit )
NOTE
Check if the cuff and hose are damaged before measuring blood pressure. A
damaged apparatus may cause inaccurate results.
A patient’s movement during measurement may cause inaccurate results.
Choose the cuff type which is appropriate to the patient.
NOTE
Do not use the NIBP Cuff for other purposes except blood pressure measurement.
Blood pressure cannot be measured on the upper arm of the patient, in case the
artificial infusion set or catheter is inserted.
WARNING
Patient Monitor
44 Blood Pressure Measurement SpO2 Measurement 45
Guardian Series
(2) Change of NIBP Mode▶ To change the setting of NIBP mode, push the Menu button to select NIBP.
▶ By operating as detailed above, you can select each function of the NIBP mode.
Set Mode Range for Change
AUTO
INTERVAL
LIST
CALIBRATION
ON / OFF
2 ~ 120 min
SYS / DIA / MEAN
-
Explanation
Select automatic or manualmeasurement
Select the time interval, when set toautomatic measurement
Indicate measuring value before 30
Contact to the agency.
SpO2 Measurement
The concentration of oxygen saturation means the saturation level of hemoglobin which can
transport the oxygen of the arterial blood. The current transport level for the capacity of
hemoglobin to transport the oxygen is expressed as a percentage.
(1) How to Measure SpO2
After measurement NIBP, if the “EXIT” button is pressed, the measured value is
disappeared on the display. (The measured value is normally saved in the Trend)
NOTE
While the MRI is used, measurement using the sensor may cause severe burning.
If this occurs during normal use, remove the product immediately from the
patient.
Do not place the probes at the site where the arterial catheter or the venous
infusion set is connected.
For neonates, measurement should be made outside the incubator using the
disposable sensor. (Humid conditions in the incubator may affect the
measurement, resulting in inappropriate data.)
NOTE
Strong light interferes with accurate measurement. In this case, cover the sensor
with an opaque material.
For patients with thick or dark skin, or with weak blood flow and weak signs, the
oxygen concentration level may appear lower than it is.
In patients with abnormalities in the peripheral nervous system including
hypothermia, hypovolemia, hyperdynamia of vessels or reduction in heart rate, the
vital signs may not read properly due to these abnormalities.
In patients with an abnormal increase in oxyhemoglobin or methemoglobin, the
data for SpO2 will not be accurate.
Check if the sensors release light, if the sensors are positioned properly opposite,
and if the light release to the patient’s tissue.
CAUTION
The automatic measurement mode (AUTO pressing) is cancelled in the following cases:
■When the blood pressure measurement fails 3 consecutive times.■When overpressure occurs. (Cuff pressure over 280 mmHg)■When the power is On/Off.
When the automatic measurement mode is cancelled, the user should reset the
AUTO pressing to let it operate normally.
WARNING
Patient Monitor
46 SpO2 Measurement SpO2 Measurement 47
Guardian Series
Connect the SpO2 probe to the connection terminal of the measurementmodule.
Step 1
Attach the probe to the finger. (If measured with NBP at the same time, theSpO2 probe should be positioned on the opposite arm. Concurrent use of othermedical devices affecting blood flow should be avoided. The probe should beattached at a site that avoids those affected by medical interference.)
Step 2
For stable measurement, have the patient minimize their movement and bandthe probe cable with the finger. Care should be taken to not let the bandinginterfere with blood flow.
Step 3
(2) Change of SpO2 Mode▶ To change SpO2 mode, push the Menu button to select SpO2.
▶ By operating as detailed above, you can select each function of the SpO2 mode.
Set Mode Range for Change
GAIN
SPEED
TRACE
x1, x2, x3 OPTIMUM
6.3, 12.5, 25 mm/sec
ON / OFF
Explanation
Set the size of SpO2 waveform
Set the speed of SpO2 waveform
Set the display of waveform
Patient Monitor
48 Body Temperature Measurement Body Temperature Measurement 49
Guardian Series
Body Temperature Measurement
Changes in impedance according to the change in the patient’ s body temperature is perceived by
the temperature sensor, and then displayed numerically on the screen after a series of calculations.
(1) How to Measure Body Temperature
MENUECG ▶
SpO2 ▶
IBP ▶
NIBP ▶
RESP ▶
CO2 ▶
ALARM ▶
SETUP ▶
EXIT ▶
ALARMHR ▶
ST ▶
SpO2 ▶
IBP ▶
NIBP ▶
RESP ▶
TEMP ▶
EtCO2 ▶
+Return
HRHIGH ▶ 39LOW ▶ 30SOUND ▶ ON+Return
HIGH LIMIT[Push Encoder] 39 20-49
Connect the temperature sensor to the connection terminal of the measurementmodule.
Step 1
(2) Change of TEMP Mode▶ To change TEMP mode, push the Menu button to select Alarm
▶ By operating as detailed above, you can select each function of the TEMP mode.
Set Mode Range for Change
High limit
Low limit
ON / OFF
20 ~ 49℃
10 ~ 40℃
ON, OFF
Explanation
Set the maximum limit of alarm
Set the minimum limit of alarm
Alarm ON, OFF
The temperature sensor provided with the product is of the rectal type.
The temperature sensor should be sterilized before application to another patient.
NOTE
Press Measurement (Optional) 51
Guardian SeriesPatient Monitor
50 Press Measurement (Optional)
Press Measurement (Optional)
(1) Press Setting
A transducer which can be protected from electric shock and electrical impulses should be used. It
can be used during the electric operation of the device.
During defibrillation of a patient, the measurement values may be inaccurate. After defibrillation
and a continuous normal state, accurate measurement values will return.
Composition of Monitoring Accessories
Connect the monitor interface cable to the press connection terminal of themeasurement module.
Step 1
In a clean environment, open the package to check if all parts are wellconnected and if the handle of the stopcock is positioned properly.All side ports of the stopcock are protected by the outlet plugs and may not beremoved till the system is full and the foam have been removed. These outletplugs should always be replaced with other outlet plugs. (A pouch is includedin the kit.)
Step 2
Connection of the converter interface cable
1. Hold the backside of the clear cover surrounding the connector, and connectthe converter to the reusable monitor interface.
2. Push the connecter gently into position. If it is well connected, the tap of theconverter connecter will fit the slot of the reusable connecter snugly.
Step 3
Only the transducer specified by the company can be used.
NOTE
Do not reuse the disposable transducer.
WARNING
Patient Monitor
52 Press Measurement (Optional) Press Measurement (Optional) 53
Guardian Series
Blood pressure for a liquid infusion line over 300mmHg requires an infusion of more than
3cc per hour. In this case, the blood pressure must not exceed 15psi (775mmHg). A
protective function is set in the flush device, which prevents overpressure of the converter
by making the liquid bypass the device. If a more precise control of fluid volume is
required, it is necessary to connect the infusion pump around the flush device.
Priming and TipsStep 5
3. To remove the converter from the cable, push the tap gently inside the clearcover and then separate the reusable interface cable.
Hold both sides of the flush operator and pull upward gently.Do not revolve the operator and take care not to put the power on one side.
Step 4
Priming should be done slowly! - Slow priming will lessen the effort to remove air bubbles
afterward.
Prime using gravity! - Pressing may result in leakage of liquid or bubbles by forcing the liquid to
flow into the system. If small bubbles flow too slowly inside the system, lift up the supply bag.
1 inch corresponds to 2mmHg, and the primed 4-feet line gives a pressure of about 100mmHg if it
is completely spread out The solution bag should be placed at a higher position than the converter
and the pressing tube, in order for priming using gravity.
1. Twist the sterilized solution bag lightly using a drip chamber spike.
2. Open the roller clamp and remove the air inside the bag completely by squeezing using an
infusion set or an 18-gauge needle inserted into the injection port in the back. By emptying the
back this way, it can prevent air input into the patient’s body.
3. Before inputting the solution into the infusion set, push both sides and fill the drip chamber
partially.
4. Operate the flush device gently. Since air rises from the bottom, make sure that the solution is in
the bottom at all times.
5. Prime the side ports and the plug of the zero point stopcocks in the converter using a door-lock
plug. <Caution: The stopcocks of the converter or the outlet should be locked before connecting
the door-lock plug.>
6. Check if bubbles are present in the monitoring system. To check the presence of invisible
bubbles, rap it lightly.
Transducer Connecting piece Monitor Interface Cable
Do not use the blood pressure monitoring kit with the nonseparated blood
pressure monitor. Do not twist the cable. Reusable interface cable cannot be
sterilized by autoclaving.
NOTE
If a fast flush is performed on the patient, the user should check carefully for the
presence of foam and particulate matter. If a large volume is flushed by force, a
short flush with an increase rate less than 2cc is recommended to avoid central
embolism.
CAUTION
Patient Monitor
54 Press Measurement (Optional) Press Measurement (Optional) 55
Guardian Series
7. Add pressure to the system up to 300mmHg using C-fusor or the clear cuff. Flush the system
for 2~3 seconds. Check for the presence of air bubbles which may result from a fast flush. Now,
the system is ready for zero point setting and measuring. Place the stopcock in a 90 degree
position to let it off state.
Be sure to never position it at 45 degrees. A wrong setting of the stopcock handle may cause
infection, bleeding, or air embolisms in the patient.
Adjustment of Zeropoint of the ConverterStep 6
1. Place the zeropoint port at the area of the right atrium, the middle of the axilla, and the fourth
intercostals area, and then place the converter and the kit in a proper operating site. Some
version of the blood pressure conversion kit is provided with the patient’s IV rod or the
accessories needed for various settings.
2. Lock the zeropoint stopcock (toward OFF) and release the converter according to the air
pressure.
3. Conduct zeroing by pushing the zeroing button of the module or select zeroing-one from the
menu in the IBP setting menu.
If the fix plate is used, fix it as below.
ABP
CVP
ICP
PAP
Arterial blood pressure
Central venous pressure
Intracranial pressure
Pulmonary arterial pressure
Artery group throughout the wholebody (systemic)
Central vein / atrium group
Intracranial group
Pulmonary artery group
(2) Change of IBP Mode▶ To change IBP mode, push the Menu button.
< Table for labels according to the site of measurement> >
Care should be taken not to let air bubbles inside the 3-way outlet stopcock or the
cannula reflush into the patient. To check, confirm if the monitoring line is fully
filled with liquid before connecting the monitoring line and let a small volume of
blood flow through the cannula.
CAUTION
Patient Monitor
56 Press Measurement (Optional) EtCO2 Measurement (Optional) 57
Guardian Series
Set Mode Range for Change
SPEED
LABEL
* ZERO
SCALE
TRACE
6.3, 12.5, 25mm/sec
ABP, CVP, ICP, PAP
ON
OPTIMUM / FIXED
ON / OFF
Explanation
Set the speed of IBP waveform
Set the level according to themeasurement site of BP.
Change the alarm setting rangeaccording to level.
Adjust the zeropoint of the transducer
Set the wave scales
Set the display of waveform
MEDEX
MX 9504T
MX 95104
MX 240
MX 800
Explanation
IBP D.P.T Monitor kit
IBP Cable
IBP Clamp
IBP Plate
▶ By operating as detailed above, you can select each function of the IBP mode.
* Adjust the zeropoint of the transducer : In order to obtain accurate results, make sure to adjust
the zeropoint of the transducer before measuring the patient.
** Fixed : Basic value according to the established label (ABP:0~200, CVP:0~50, ICP:0~50,
PAP:0~50)
*** Optimum : Scale of waveform is automatically adjusted regardless of the level.
<Composition of IBP KIT >
EtCO2 Measurement (Optional)
(1) CO2 Gas MeasurementNot only Mainstream CO2 but also Sidestream CO2 can be installed in Guardian
Those Mainstream/ Sidestream CO2 provides the function of ETCO2, the respiratory CO2, the
function to measure respiration rate.
The display and menu about EtCO2 are automatically reconstituted depending on attachment
or detachment CO2 module.
(2) Sidestream CO2
A. Connect one side of the gas outlet to the gas outlet of Guardian and the other side to the air
elimination system of the hospital.
B. Open the spring-type door and connect the filterline appropriately to the equipment. The
other end is then connected to the patient.
C. Respiratory rate is automatically changed during measuring EtCO2. The calculated value of
the chest impedance change is shown in case of stop measurement.
The maximum sampling rate of the nose tube is 50mL/min. The product should
not applied to patients who may experience respiratory distress by the vacuum
flow level.
To prevent infection of the medical staff by the patient’s respiration sample, the
outlet of Guardian should be connected to the air elimination system of the
hospital.
WARNING
The gas inspiring vacuum pressure (negative pressure) of the gas elimination
system should not exceed the pump outlet standard of Guardian, 1mmHg.
Excessive pressure will display the message of “OCCULSION” and it may
damage the Guardian product pump. During zeroing, the air elimination system
should be operating.
WARNING
Patient Monitor
58 EtCO2 Measurement (Optional) EtCO2 Measurement (Optional) 59
Guardian Series
D. If GUARDIAN senses proper respiratory movement, it displays the level of EtCO2,
inspired CO2, and respiration rate.
E. The respiratory waveform and data of EtCO2 is displayed. If the waveform does not appear,
set the Menu --> EtCO2 ---> TRACE --> ON.
F. If necessary, the size of the CO2 waveform can be adjusted by using the menu.
(3) CO2 CALIBRATIONThe accuracy validation for the CO2 should be performed once a year or when the
measurement results are not accurate.
A. Select EtCO2 --> Calibration by pressing MENU button
B. It is starting Calibration with message “Zero in Progress” on display of EtCO2 Wave
C. If the message “Zero In Progress” is disappeared, the Calibration is normally completed.
Massage
Wait For Sensor
Check Adaptor
Zero Require
Explanation
Self initialization process of EtCO2 module when power is on(the measurement may be inaccurate during this period)
Not connected to the accessory
Need the Calibration
* During Measurement mode
Massage
Zero In Progress
Explanation
Progressing the CALIBRATION
* During Calibration mode
Connection of all tubes should be safe, and the nose cannula should be kept away
from the CO2-present area during the warming up period (including the outlet of
the ventilator and the respiration of the user).
Range for Measuring : 0 ~ 150bpm
NOTE
For the best accuracy, a warm-up of about 20 minutes is required.
NOTE
Refer to the following diagrams during the EtCO2 measurement.
NOTE
CO2 waste and CO2 filter should be treated as fatal biological materials for the
human body.
CAUTION
Patient Monitor
60 Before Requesting After-Sales Service Before Requesting After-Sales Service 61
Guardian Series
Before Requesting After-Sales Service
This section shows how to treat simple problems encountered during use.
Please check the following points before requesting after-sales service.
Sign
The power of the product isnot turned on.
The power of the product turnsoff suddenly during use.
The power of the product isnot turned on.
The waveform is not normal.
1. Check if the AC power is supplied..2. Press and hold the power button for 2 seconds
1. Check if the power is off due to battery release.2. Check if AC power is supplied to the product.
1. Press the power button during 1~2 seconds2. Check if “Power off” message is shown in display.
1. Check if there is any equipment with a strong magnetismaround the product.
2. Check if the cable connection is stable.3. Check if the product is grounded.
How to treat
Sign
The message “LEAD FAULT”is displayed.
The ECG waveform is notdisplayed.
Severe noise on thewaveform.
1. Check the ECG cable and ensure that the gel in theelectrode is not dry.
2. Try using another ECG cable.
1. Check if the cable connection is stable.2. Check if the ECG cable is damaged.
1. Check if the electrode attached to the patient is stable.2. Check if the disposal electrode is one provided by the
company. (Noise may occur according to the kind ofelectrode.)
How to treat
▣Problems in Display
▣Problems in ECG / Respiration Measurement
Sign
SpO2 measurement isunstable.
1. Check if the probe is affected by strong light in the area.2. Check if the connection is normal; if the red light of the
sensor flickers or does not turn on, it is an inferior probe.3. Check if there are any factors interfering with the patient’s
blood flow. (For example, if the device is connected to thearm being measured for blood pressure, or if the probe isbanded on the finger for too long a time.)
4. Check if the probe is properly positioned to the patient.5. Check if the patient is shaking their finger or pressing the
probe.6. Check if the probe is damaged.
How to treat
Sign
NIBP measurement isunstable.
1. Check if air has leaked out due to bending or damage ofthe NIBP cuff or hose.
2. Check if the proper type of cuff is used for the patient.3. Check if the posture of the measurement site is proper.4. Check if the patient moves during measurement.5. Check if the cuff is attached too loose or too tight.
How to treat
▣Problems in SpO2 Measurement
▣Problems in NIBP Measurement
Patient Monitor
62 Before Requesting After-Sales Service Product Specifications 63
Guardian Series
Sign
Blood pressure measurementis unstable.
Severe noise or bias in thewaveform.
Pour out the contents of the tube carefully and remove thebubble, then shorten the tubing length.
Do not shake or touch the connection area of the IBP sensor.
How to treat
▣Problems in IBP Measurement
Sign
Check Adaptor
The wave and value of EtCO2 is not displayed
The Filterline is not connected to the main body.Connect the Filterline.
Check if the sampling line and filter is obstructed, and clean itup if possible. It should be changed if necessary. To removethis message, disintegrate the filterline and then reconnect it.
How to treat
▣Problems in EtCO2 Measurement
Sign
No printing.
Noise during printing.
1. Check if the message “PRINTER” is displayed on thescreen.
2. Check if the power LED lights up on the printer.3. Check if the paper is set normally.4. Check if the printer door is closed.
1. Check if the roller is contaminated with foreign materials orif the gear is out of position.
2. Check if the problem is due to a paper jam (change thepaper)
How to treat
▣Problems in EtCO2 Measurement(Optional)
Product Specifications
1) Measurement parameters- ECG, NIBP, SpO2, Respiration, IBP, Temp, EtCO2
- PROCESSING PARAMETERS :
HR, NIBP(Systolic/Diastolic/Mean pressure), SpO2 Saturation, Pulse rate, Respiration, IBP,
Temp, EtCO2
2) Monitor Performances specifications- TFT Color LCD Display
- Waveform Display Method : Scroll
- Display Size : 7 inch
- Resolution : VGA (800X480)
- Sweep Speed : 6.3, 12.5, 25mm/sec
- Display waveform Time : 4 sec
- Waveform Freeze : Function of waveform freeze
- Waveform Display : ECG, SpO2, IBP, Respiration , EtCO2
- Waveform Traces : 6 Traces
- Measurement Value Display : Heart Rate, SpO2, Pulse Rate,
NIBP, IBP, Temp, Respiration
EtCO2, FiCO2
3) ECG Measurement- ECG Lead : 3 lead / 5 lead( I, II, III, aVR, aVL, aVF, V )
- Input : Installed the circuit for protecting from the high frequency electric potential of ESU,
Defibrillator and so on.
Patient Monitor
64 Product Specifications Product Specifications 65
Guardian Series
- Frequency Filter : High frequency noise remove filter / Install the
50/60Hz power noise remove filter
- Input Impedance : Greater than 5 M ohm(50/60Hz)
- Input for Initial Electric currency : Below 50 ㎂
- CMRR : Greater than 120dB
- Frequency Bandwidth : 0.5 ~ 40 Hz, 0.5Hz ~ 80Hz, 0.05Hz ~ 40Hz, 0.05Hz ~ 80Hz,
1.0Hz ~ 40Hz, 5.0Hz ~ 20Hz,
- Gain : 5, 10, 15 mm/mV
- QRS Sensing Range : -0.5mVpp ~ + 5mVpp
- ST-Level : -0.1mV ~ +0.1mV(High limit : 0.01mV~0.99mV,
Low Limit : -0.99mV~ 0.01mV)
- Alarm Setting Range : High Alarm Limit : 10~300bpm ,
Low Alarm Limit : 5~295bpm
- ARRHYHMIA Detect
① Asystole
② Ventricular Tachycardia
③ Ventricular Bradycardia
④ Ventricular Fibrillation
⑤ PVC
⑥ R-on-T
⑦ Missed Beat
⑧ Tachycardia
⑨ Bradycardia
⑩ Bigeminy
⑪ Trigeminy
⑫ Couplet
4) Heart RATE- Measurement Range : 20 ~ 300bpm
- Accuracy : ±2bpm (Measurement value)
- Alarm Range : High alarm limit - 10 ~ 300, OFF, Low alarm limit - 5 ~ 295
5) SpO2, Pulse Oximetery- Measurement Range : 20 ~ 100%SpO2
- Accuracy : 70 ~ 100% SpO2 : ±2%
50 ~ 69% SpO2 : ±3%
0 ~ 49% SpO2 : Unspecified
- Alarm Range : High limit - 21 ~ 99%, OFF SpO2
Low limit - OFF, 20 ~ 98% SpO2
- Pulse Measurement Range : 20 ~ 300bpm
- Pulse Measurement Accuracy : ±2 bpm
6) Non-invasive Blood Pressure Measurement- Measurement Method : Oscillometric, Automatic measurement
- Display Value : Systolic, Diastolic, Mean Pressure
- Measurement Range :
- Accuracy: 0~200mmHg : ±3mmHg , 200~270mmHg : ±4mmHg
- Range: 0~300mmHg
- Alarm Range
- Auto Pressure: Manual, Automatic (2~120 minutes interval)
- Measurement Sensitivity : 1mmHg
7) Respiration- Measurement Range : 2 ~ 150 rpm
- Accuracy : ±2 rpm
- Measurement Sensitivity : 1rpm
- Alarm Range : High limit : 5~149 / Low limit : 1~145
Display
NIBP[mmHg]
Systolic
Diastolic
Mean
SYSTOLIC 60~270mmHg 50~130mmHg
MEAN 45~255mmHg 40~120mmHg
DIASTOLIC 40~245mmHg 30~100mmHg
PRESSURE ADULT NEONATE
High
40 ~ 295, OFF
30 ~ 285, OFF
35 ~ 290, OFF
Low
OFF, 30 ~ 290
OFF, 25 ~ 280
OFF, 30 ~ 285
Patient Monitor
66 Product Specifications Product Specifications 67
Guardian Series
8) IBP (Invasive Blood Pressure) - Optional- Measurement Range : -40 ~ 360mmHg
- Accuracy : ±2mmHg
Measurement Sensitivity : 1mmHg
- Alarm Range : ABP standard
9) Temperature- Measurement Range : 10 ~ 50℃
Measurement Sensitivity : 0.1℃
- Accuracy : ±0.1℃
- Alarm Range : High alarm limit - 20.0℃ ~ 49.0℃, OFF
Low alarm limit - 10.0℃ ~ 40.0℃
10) EtCO2 : End-Tidal CO2 - Optional- Transducer Type: Mainstream / Sidestream CO2 Sensor
- Range: 0~150mmHg
- Temperature: Normal temperature 0~45℃
- Accuracy :
- Alarm Setting Range : High limit: 2~99mmHg , Low limit : 1~98mmHg
11) Printer - Optional- Print Method : Thermal
- Type : Internal
- Paper Width : 57 mm
- Valid Width : 120 ~ 300mm
12) Trend- Parameter : Heart Rate, SpO2, Pulse Rate, NIBP, IBP , Temperature, EtCO2
- 72 Hours (1 minute step : Saving Data 4,320ea)
13) Interface- RS-232C port
- LAN Port (Central Monitor)
- VGA Port (Display Transferring)
14) Physical Specifications- Size: 205 x 207 x 147mm (WxDxH)
- Weight: 2.4Kg(Include battery)
- Power Requirement: AC 100~240V , 50/60 Hz, 90VA(MAX)
- Battery: LI-Ion, 11.1V, 4400mAh
15) Operating Environment- Temperature : (Operating : 10℃ ~ 45℃ / Storage : -10℃ ~ 50℃)
- Humidity : (Operating : 30 ~ 85% / Storage : 20 ~ 95%)
- Atmospheric Pressure : (Operating : 70 to 106 kPa / Storage : 70 to 106kPa)
Display
IBP[mmHg]
Systolic
Diastolic
Mean
High
40 ~ 295, OFF
30 ~ 285, OFF
35 ~ 290, OFF
Low
OFF, 30 ~ 290
OFF, 25 ~ 280
OFF, 30 ~ 285
CO2 Density
0~40mmHg
41~70mmHg
71~100mmHg
101~150mmHg
Accuracy
±2mmHg
±5% of reading
±8% of reading
±10% of reading
Patient Monitor
68 Product Specifications Product Warranty 69
Guardian Series
16) Standard Accessories- 5lead ECG cable 1 ea
- Adult NIBP cuff 1 ea
- Gray hose 1 ea
- Power cord 1 ea
- Adaptor 15V 3Ah 1 ea
- Disposable Electrode (5pcs/set) 1 set
- SpO2 Sensor (Reusable) 1 ea
- Battery 11.1V 4.4Ah(built-in) 1 ea
- Temp. sensor(Rectal type) 1 ea
- User Manual 1 ea
17) Optional Accessories- 3lead ECG Cable
- Extension Cable for SpO2 sensor
- IBP module kit
- Printer Module
- Roll Paper
- EtCO2 Kit set (In case of EtCO2 installation)
- Disposable Electrode (50 PCS/1SET)
- Battery
- TROLLEY (=Rolling Cart)
- Wall Mount
- Skin Temp Probe
- Disposable SpO2 sensor
- Y-type SpO2 sensor (Clip type)
- Neonate NIBP Cuff
- Child NIBP Cuff
Product Warranty
Product Name
Model Code
Manufacture Approval No.
Manufacture Approval Date
Manufacture Serial No.
Warranty Period
Purchase Date
Name ofHospital
Address
Name
Tel
Thank you for using Guardian
This product is a medical device.
Only the products that have Passed our extensive and thorough quality tests are
offered to our customers
Our policies on repairing, exchange and refund complies with “Regulation on
Consumer Protection & Compensation Standards” issued by Economic
Planning Board of Korea
Name of Distributor
Name of Manufacture
CustomerInformation
Patient Monitor
BPM-770 (BRAND NAME : Guardian)
No. 10-646
JUL. 05. 2010
No. 1936
One year after the purchase date
Date Month Year
Tel) Fax)
BIONICS Co., Ltd.