BT-770 Service Manual (770-ENG-SVM-EUR-D00)

BT-770
Patient Monitor
Service Manual
BT-770
Keep this manual for future reference

P/N : 770-ENG-SVM-EUR-D00
BT-770 Service Manual 1
Proprietary Material
Information and descriptions contained in this manual are the property of Bistos Co., Ltd and may not be
copied, reproduced, disseminated, or distributed without express written permission from Bistos Co., Ltd.
Information furnished by Bistos Co., Ltd is believed to be accurate and reliable. However, 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 under any patent or
patent rights of Bistos Co., Ltd.
The information contained herein is subjects to change without notice.
Revision D00
November, 2017
Copyright © Bistos Corporation 2017. All rights reserved.
th
7 Fl., A Bldg., Woolim Lions Valley 5-cha, 302,
Galmachi-ro, Seongnam-si, Gyeonggi-do,
Korea
Telephone: ++82 31 750 0340

Fax: ++82 31 750 0344
Printed in Korea
P/N : 770-ENG- SVM-EUR-D00 Bistos Co.,Ltd 2017, 11

Table of Contents
Section 1 Safety ∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙ 3
1.1 Instructions for the Safe Operation and Use of the BT-770 patient monitor∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙ 3
1.2 General Precaution on Environment ∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙ 4
1.3 Definition of Symbols ∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙ ∙∙∙ 4
Section 2 Introduction ∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙ 5

2.1 Product Overview ∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙ 5
2.2 Options and accessories∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙ 6
2.3 Description of product∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙ 7
2.4 Product installation ∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙ 10
Section 3 Disassemble & Assemble ∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙ 11

3.1 Product disassembly view∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙ 11
3.2 Disassembly∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙ 17
3.3 Assemble∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙ 22
Section 4 Maintenance & Conservation ∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙ 23

4.1 Checking∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙ 23
4.2 Maintaining plan∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙ 23
4.3 ECG calibration∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙ 24
4.4 Touch screen calibration∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙ 24
4.5 Cleaning∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙ 24
4.6 Disinfection∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙ 25
Section 5 Troubleshooting ∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙ 26

5.1 Alarm Information∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙ 26
5.2 Machine malfunction∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙ 30
5.3 Operating & Recording∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙ 30
5.4 Battery malfunction∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙ 31
5.5 Parameter malfunction∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙ 31

Section 1
Safety
1.1 Instructions for the Safe Operation and Use of the BT-770 patient monitor
 Examine the monitor and any accessories periodically to ensure that the cable, line cords,
transducers, and instruments do not have visible evidence of damage that may affect patient
safety or monitoring performance. The recommended inspection interval is once per week or
less. Do not use the device if there is any visible sign of damage.
 Only the AC line cord supplied with the BT-770, or its equivalent, is approved for use with the
equipment.
 Do not attempt to service the BT-770 patient monitor. Only qualified service personnel by
Bistos Co., Ltd. should attempt any needed internal servicing training.
 The BT-770 is not specified or intended for operation during the use of defibrillators or during
defibrillator discharge.
 The BT-770 is not specified or intended for operation in the presence of electrosurgical
equipment.
 The BT-770 is not specified or intended for operation in conjunction with any other type of
monitoring equipment except the specific devices that have been identified for use in the
Operation Manual.
 Perform periodic safety testing to ensure proper patient safety. This should include leakage
current measurement and insulation testing. The recommended testing interval is once per
year.
 Do not operate the BT-770 patient monitor if it fails to pass the power on self-test procedure.
WARNING Can lead to serious injury or death.

CAUTION Can lead to minor injury or product/property damage
Can lead a potential hazardous situation which, if not avoided, may result in
NOTE
minor or moderate injury

1.2 General Precaution on Environment
Avoid placing in an area

exposed to moisture. Do Avoid exposure to direct
not touch the pulse sunlight
oximeter with wet hand.

where high variation of
temperature exists.
Avoid in the vicinity of
Operating temperature
electric heater.
ranges from 5℃ ~ 40℃.
Operating humidity ranges
from 30 % ~ 85 %.

where there is an
where there is an excessive
excessive humidity rise or
shock or vibration.
ventilation problem.

Avoid dust and especially
where chemicals are
metal material enters into
stored or where there is in
the pulse oximeter.
danger of gas leakage.
Power off when the pulse

Do not disjoint or
oximeter is not fully ready to
disassemble the pulse
operate. Otherwise, the
oximeter. Bistos Co., Ltd.
pulse oximeter could be
does not have liability of it.
damaged.
1.3 Definition of Symbols
Symbol Description
Used to identify safety information.
Be well-known this information thoroughly before using BT-770.
During the operation, do not disconnect any cable.
Indicates the protection level against the ingress of liquid.
IPX1
IPX1 Protected against the vertically dripping water.
Refer to operation manual. Read manual before placing the device.
Indicates DC power supply.

Indicates the device is in the battery operation mode
Indicates a defibrillation-proof type CF applied part.
Indicates the packing material is recyclable.

Indicates to not dispose the device together with unsorted municipal waste(for EU
only). The solid bar symbol indicates that mains adapter is put on the market after
13 August 2005.
Federal law restricts this device to sale by or on the order of a physician..

CAUTION

Section 2
Introduction
2.1 Product Overview
BT-770 patient monitors mainly to complete the monitoring of physiological parameters ECG, NIBP, SpO2,
TEMP, RESP, IBP, C.O., CO2, etc. (IBP, C.O., CO2 can be optional function). In order to complete these
functions, its function is mainly divided into the following main parts :
(1) Parameter measurement part

(2) Main control part
(3) Main - machine interface part
(4) Power part
(5) Auxiliary function part
2.1.1 Parameter measurement part

Parameter measurement and monitoring are the core functions of the system. BT-770 patient monitor
parameter measurement part of the function by the measurement probe, parameter input socket and the
main control board.
Its role is to pass the physiological signal collected by the probe into electrical signal, according to the
pre-set program or the main control part of the transmission of the order, to deal with the signal
processing and calculation, then send the value, waveform and alarm information to the main control part,
and then use the man-machine interface, displayed it.
2.1.2 Main control part

In the BT-770 patient monitor, the main control part refers mainly to the main control board. Its main
function is power management allocation, drive man-machine interface, management parameter
measurement and provide users with other special features, such as storage, waveform, data review, etc.
2.1.3 Main – machine interface part

BT-770 patient monitor man-machine interface includes a display, recorder, speakers, indicator light,
buttons, encoders and touch screen, etc.
• The display is mainly to provide users with a large number of real-time and historical data and
waveforms, and provide a variety of information and alarm tips
• The recorder is a supplement to the display screen that allows the operator to print out various
data.
• The speaker mainly provides sound alarm function.
• The indicator light provides additional information on power, battery, alarm, and so on.
• Keys, encoders, and touch screens are user input interfaces through which users can enter
information and instructions into the monitor.
2.1.4 Power part

• Power is an important part of the system, including the power adapter and battery two parts.
• The power adapter converts AC mains into a 15V DC low voltage power supply to provide
energy to the system.
• The battery provides a short period of time when the system is not energized.
2.1.5 Auxiliary function part

BT-770 Patient monitor also provide U disk upgrade function, allowing service user to upgrade and
update the software without disassembly the machine.

2.2 options and accessories

Picture Name Description Qty
ECG cable and

lead wire Measures ECG 1ea
(standard)
ECG electrode
Electrode for ECG measurement 1ea
(standard)
Adult SpO2
sensor SpO2 sensor for adult 1ea
(standard)
SpO2 extension
Cord to connect the SpO2 sensor and
cord 1ea
main body
(Standard)
Adult NIBP cuff

Measures NIBP for adult 1ea
(standard)
NIBP extension
Tube to connect the NIBP cuff and
tube 1ea
main body
(standard)
Temperature
sensor Measures the body temperature 1ea
(Standard)
Adapter
For power supply 1ea
(Standard)
CO2 sensor
Measures the CO2 1ea
(Optional)

2.3 Description of Product
2.3.1 Description of the BT-770 Front
Name Description
Indicates the priority of physiological alarm and technical
alarms in different colors and flashing frequencies.
1 Alarm indicator - High priority: Red, fast flashing (1.4 ~ 2.8 Hz)
- Medium priority: Yellow, slow flashing (0.4 ~ 0.8 Hz)
- Low priority: Yellow, constant on
2 Display area Display the waveform and measured value
- Power On: Press down the key more than 2 seconds.
- Power Off: Press down the keys more than 2 seconds
3
[Power] and the system will display the alarm message “The
system will shut down 3 seconds”.
- On: The battery is being charged or has been fully
charged.
4 Battery indicator
- Off: The battery has not been installed.
- Flashing: The monitor is being powered by the battery.
Turned on when the monitor is being powered by the
5 DC power indicator
adapter.
6 To reset the alarm condition.

[Alarm reset]
To pause the alarm sound. Alarm pause time can be set
7 as 1 , 2, 3, 4, 5, 10, 15 minutes, and permanent. Default
[Alarm pause] setting is 2 minutes.
Start and stop the non-invasive blood pressure
8
[NIBP start/stop] measurement.
Rotate: move the cursor.
9 Control knob
Press: select the menu or execute a command.
Enter to the setting mode. Press again to close the
10
[Setting] setting mode.
11 Freeze/unfreeze the waveform.

[Freeze]

2.3.2 Description of the BT-770 side
Name Description
1 SpO2 SpO2 cable interface

2 T1 Temperature probe interface
3 T2 Temperature probe interface
4 ECG ECG cable interface
5 NIBP NIBP cuff interface

2.3.3 Description of the BT-770 Rear
Name Description
1 Handle Handle for main body transport
2 Speaker holes For alarm and synchronizing sound
3 Air outlet Heat dissipation
4 Battery cover Battery compartment cover
5 Bracket To wall mount the monitor
6 ID label Identify the monitor information
7 Air intake For ventilation

Auxiliary output
8 Nurse call
interface
9 Network port For CMS
10 USB port For trend or software upgrade
11 Power adapter 15V, 2.4A adapter

2.4 Product installation
2.4.1 Turn on
2.4.1.1 Check the patient monitor

• Before turn on the pulse oximeter, check whether there is mechanical damage to the pulse
oximeter, and whether the external cables and accessories are connected correctly.
• Plug the power adapter into the AC power outlet. If using battery power, make sure the battery is
fully charged.
• Check all the functions required to make sure that the pulse oximeter operates properly.
WARNING
If the pulse oximeter is damaged, or fails to work normally, do not use it. Please contact
the maintenance personnel or Bistos immediately.
2.4.1.2 Start the patient monitor
If finish to check the pulse oximeter, it is ready to start the patient monitor.
Press the [Power] key, the yellow warning lights flash once and the system enter the program
reading interface; finally the system makes a “tick” sound, the boot screen disappears, and the system
enters the main interface.
• If any fatal error occurs during self-test, the system will alarm. If this case persists, please stop to
using the pulse oximeter and contact the maintenance personnel or Bistos.
• Check all available pulse oximeter functions to ensure that the pulse oximeter operate properly.
• If the pulse oximeter equipped with a battery, charge the battery after each use to ensure
sufficient power.
• After unpacking and use the pulse oximeter at first time, the pulse oximeter should be powered
with adapter.
2.4.1.3 Connect the sensors

Connect the required sensor to the monitor and the monitoring site of patient.
2.4.1.4 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, such as patient type.
• For the details of parameter measurement or monitoring, see the appropriate section.
• The operator can operate according to their own habits, standing in front, left or right of the
monitor, easy to observe and operate the monitor.
2.4.2 Turn off

Turn off the patient monitor in the following steps
• Disconnect the cables and sensors connected to the patient.
• Press and hold the [Power] key for 2 seconds to pop up the 3 seconds countdown window,
and the patient monitor turns off in 3 seconds.
CAUTION
If the pulse oximeter is not turned off properly, you can simply disconnect the power to
shutdown forcibly. But the forced shutdown may cause data loss, and it is not
recommended.

Section 3
Disassemble & Assemble
This manual contains technical details for the BT-770 patient oximeter. It provides a technical foundation
to support effective troubleshooting and repair. It is not a comprehensive, in-depth explanation of the
product architecture or technical implementation. It offers enough information how to repair the patient
oximeter.
Only qualified service personnel should attempt to install the system, disassemble the monitor, remove or
replace any internal assemblies, or replace the transducer cable.
3.1 Product disassembly view
3.1.1 BT-770 Disassembly view Front & Rear
No. Name & Specifications QTY(EA)

1 BT-770 Front shell component 1
2 BT-770 Rear shell component 1
3 M3X6 Stainless steel Phillips pan-head screws 5

3.1.2 BT-770 Disassembly view of Front

1 BT-770 Display screen component 1
2 BT-770 screen stent component 1
3 M3X6 stainless steel Phillips pan head screws 1
4 M3X6 Cross pan head combination screws 5

3.1.3 BT-770 Disassembly view of display

1 BT-770 Facial panel 1
2 BT-770 Front shell 1
3 Alarm lampshade 1
4 PA3X8 crosshead with pad tapping screws 4
5 Alarm light board 1
6 12.1inch LCD Display screen 1
8 Photoresistance 1
9 Encoder knob 1
10 Encoder board 1

3.1.4 BT-770 Disassembly view of display stent

1 BT-770 Display screen stent 1
2 Integrated parameter board 1
3 Main control board 1
4 Serial port expansion board or Video transfer board 1
5 IBP module or IBP/CO module 1
（Optional，if configuration IBP or CO）
6 M3X6 Cross pan head combination screws 16

3.1.5 BT-770 Disassembly view of rear

1 BT-770 Rear shell 1
2 Lithium battery 1
3 Battery cover 1
4 Hookup 1
5 Hookup screw 1
6 Speaker 1
7 Parameter socket board component 1
8 Interface board 1
9 Foot pad 2
10 Plug box connector 1
11 Side cover 1
12 M3X6 Stainless steel crosshead screw 4
13 PA3X8 crosshead with pad tapping screws 4
14 Ø3 Big flat pad 4

3.1.5 BT-770 Disassembly view of

1 Parameter socket board（2 IBP） 1
2 TEMP inside cable 1
3 SpO2 Machine internal fixed block 1
4 PB3X8 crosshead head tapping screws 1
5 ECG inside cable 1
6 IBP machine inside cable 2
（Optional，if configuration IBP or CO）
7 SpO2 inside cable 1
8 NIBP gas mouth 1

3.2 Disassembly
It should be unplugged the power and turned off the machine before disassembly patient monitor.
3.2.1 Disassembly product

Remove the 5pcs M3 × 6 stainless steel Phillips pan head screws with the front and rear shell
components from the back of the machine and remove the wires and tubing connected to the front
housing assembly with a Phillips screwdriver, you can split the machine into front shell and Rear shell
components in two parts, as shown below.

3.2.2 Disassembly battery

Unscrew the M3×6 Stainless steel crosshead screw with a Phillips screwdriver to remove the battery
cover and remove the battery cover.
Pull out the battery, pull out the battery docking wire and then can remove the battery, as shown below:

3.2.3 Disassembly rear Ass’y
3.2.3.1 Disassembly the parameter socket board component

Use a Phillips screwdriver to remove 3pcs M3 × 6 Stainless steel crosshead screw to remove the
parameter socket board component.
3.2.3.2 Disassembly interface board

Use a Phillips screwdriver to remove 2pcs PA3 x 8 crosshead with pad tapping screws to pull out the
interface board.
3.2.3.3 Disassembly Plug box connector

Use a Phillips screwdriver to remove 2pcs M3 × 12 Stainless steel crosshead screw to remove the plug
box connector.
3.2.3.4 Disassembly speaker

Use a Phillips screwdriver to remove 2pcs PA3 x 8 crosshead with pad tapping screws and can remove
the speaker

3.2.4 Disassembly PCB board
3.2.4.1 Disassembly main control board

Unplug the cable connected to the main control board, with a Phillips screwdriver to remove the fixed
main control board of the 4pcs M3 × 6 Cross pan head combination screws, you can remove the main
control board, as shown below.
3.2.4.2 Disassembly video transfer board

Unplug the cable connected to the video transfer board, use a Phillips screwdriver to remove the fixed
video adapter board 4pcs M3 × 6 Cross pan head combination screws, you can remove the video transfer
board, as shown below.
3.2.4.3 Disassembly integrated parameter board

Unplug the wire connected to the integrated board and replace the 4pcs M3 × 6 Cross pan head
combination screws with the Phillips screwdriver to remove the integrated parameter board, as

3.2.5. Disassembly display
Unplug the cable on the display screen, use a Phillips screwdriver to remove the 5pcs M3 × 6 Cross pan
head combination screws and 1pcs M3 × 6 crosshead pan head screw with the fixed frame bracket to
remove the screen bracket as shown below
With a Phillips screwdriver to remove the fixed display of the 4pcs M3 × 6 cross pan head screws, you
can remove the display and touch screen, as shown below.

3.3 Assemble
Assemble the device in the reverse sequence of disassembling.

Section 4
Maintenance & Conservation
BT-770 Multi-parameter Patient Monitor is a sophisticated, sophisticated electronic instrument. Good
maintenance of monitor can not only play the best performance of the machine, but also to ensure the
accuracy of long-term work and avoid a variety of measurement error. To prevent cross contamination,
make sure that the machine has been cleaned and disinfected before maintenance.
• If the user in the various hospitals or institutions can not implement a

satisfactory maintenance plan when use this monitor, it will cause function
WARNING
failure, and may endanger human health.
4.1 Checking
Before using the monitor, the following basic inspection work should be carried out:
• Check for any mechanical damage.
• Check all exposed wires, insert parts and accessories.
• Check all functions that may be used to monitor the patient and ensure it in good working
condition
Check all instrument functions that may be used to monitor the patient and ensure that the instrument is
in good working condition.
If you find evidence that the instrument is damaged, you may not use this monitor to perform any care on
the patient. Please contact your hospital's professional maintenance personnel or our customer service.。
All inspections that require disassembly the instrument must be carried out by qualified service personnel.
Safety and maintenance inspections may also be carried out by personnel of the Company.
Every 6-12 months or after each repair, the machine must conduct a comprehensive inspection of the
equipment by trained and qualified technical service personnel, including functional safety checks,
specific check items are as follows:
• Whether the environment and power supply meet the requirements.
• Whether the equipment and accessories have mechanical damage.
• Whether the power supply is worn and the insulation performance is good.
• whether to use the specified attachment。
• Whether the function of the alarm system is normal.
• Whether the performance of the battery meets the requirements.
• Whether the various monitoring functions are in good working condition.
• Whether the grounding impedance and leakage current meet the requirements.
4.2 Maintaining plan
The following tasks can only be approved by the company's professional maintenance staff to complete。
Please connect with maintenance staff if need the following services. It should be cleaned and disinfected
Before testing or maintenance

4.3 ECG calibration
During the use of the monitor, due to hardware or software problems, the displayed ECG signal may
appear inaccurate. Mainly for the waveform amplitude becomes larger or smaller. At this point, you need
to calibrate the ECG.
Preparing the following instrument before detection：
• ECG simulator。
• ECG cable and lead-wires。
• Vernier caliper。
• Calibration operation as follows：
• Connect ECG cable to monitor
• Connect ECG electrode sheet to ECG simulator.
• Choose or【Setup】 key .

• Choose【User Maintenance】→ input password “2013” and confirm.
• Choose【Module Maintenance】.
• Choose【ECG】→ choose【Calibration】to calibrate ECG.
• Measure the amplitude of the waveform with a caliper. The amplitude of the square wave is
compared with the scale, and the error range should be within 5%.
• After finished Calibration，Choose【Stop Calibration】to exit calibration.
4.4 Touch screen calibration
You can achieve touch screen calibration after following the steps below：
• Choose or【Setup】 key .

• Choose【User Maintenance】→ input password “2013” and confirm.
• Choose【Calibration Touchscreen】to enter the touch screen interface.
• Click on the different positions in the screen will appear in turn calibration mark.
After calibrated the touch screen，choose【Ok】to exist interface; if the touch screen is not fully
calibrated, choose Retry】to recalibrate.
4.5 Cleaning
The device should be cleaned regularly. In the heavily polluted environment, increase the frequency of
cleaning. Before cleaning, please consult the hospital about device cleaning requirements.
Below are available cleaning agents:

• Diluted ammonia
• Diluted sodium hypochlorite (washing bleach)
• Diluted formaldehyde
• Hydrogen peroxide (3%)
• Ethanol (70%)
• Isopropanol (70%)
Before cleaning:
• Turn off the monitor, disconnect the power cord and remove the battery.
• Use a soft cotton ball to adsorb appropriate amount of cleaning agent and wipe the display
screen.

• Use a soft lint-free cloth to adsorb appropriate amount of cleaning agent and wipe the surface of
the device.
• If necessary, use a clean, dry, lint-free cloth to remove any excess detergent.
• Dry the device naturally in a ventilated cool environment.
WARNING • Before cleaning the monitor or sensor, turn off the power and disconnect
the DC power.
• The monitor should be kept clean. It is recommended to regularly clean

the enclosure surface and the display screen. Cleaning the enclosure
with non-etching cleaner such as soap and water.
To avoid damaging the pulse oximeter.

CAUTION
• Do not use strong solvents such as acetone.
• Most cleaners must be diluted before use. Diluting should be according
to the manufacturer's instructions.
• Do not use abrasive materials (such as steel wool).
• Do not allow any liquid entering into the enclosure, and never immerse
any part of the device into liquid.
• Do not leave any cleaning solution on the surface of any part of the
device.
Note • Wipe the monitor and sensor surface with medical alcohol, dry it
naturally or with clean, dry, lint-free clot.
• Bistos is not liable for effectiveness of using these chemicals for

infectious disease control. Please consult the infectious disease control
officers or experts of the hospital for advice.
4.6 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 recommend that the instrument to
be disinfected must first be cleaned.
• To prevent damage to the monitor, do not disinfect the monitor with gas
CAUTION
(EtO) or formaldehyde.

Section 5
Troubleshooting
BT-740 patient monitor in the transport, storage, use the process, due to various factors (such as power
grid voltage instability, ambient temperature changes, falling and impact, aging components, etc.) may
affect the failure of normal use. At this time should be a certain degree of electronic medical equipment
maintenance experience with the following professionals refer to the following classification of fault
classification. The so-called component-level maintenance refers to the components through the analysis,
replacement, test run, the fault will be positioned to the instrument components, such as the power board,
the main control board, components, measuring cables or parameter modules. Parts of the maintenance
that is component-level maintenance, manufacturers must have extensive experience in the maintenance
of engineers using specialized equipment, in a specific environment and conditions.
5.1 Alarm Information

This chapter lists some important physiological and technical alarm information, and some alarms are not
necessarily listed.
Note that in this chapter: L column indicates the default alarm level: H indicates high level, M indicates
middle level, L indicates low level, and “*” indicates level set by the user.
Corresponding countermeasures are listed for each alarm message. If you operate in accordance with
the countermeasures but the problem persists, contact your service personnel.
5.1.1 Physiological Alarm Information

Source Alarm message L Causes and countermeasures
HR Too High HR value is higher than the upper alarm limit or lower
than the lower alarm limit. Check the patient's
M*
HR Too Low physiological condition, and check if the patient category
and alarm limit settings are appropriate for the patient.
PVCs value is higher than the upper alarm limit or lower
PVCS Too High M*
physiological condition, and check if the patient category
Asystole H The patient has arrhythmia. Check the patient's
VF/VTA H condition, electrodes, cables and lead wires.
R on T M*
Frequent PVC M*
Couplet PVC M*
Single PVC M*
PVC Bigeminy M*
ECG PVC Trigeminy M*
Tachycardia M*
Bradycardia M*
Miss Beat M*
Pacemaker Not Capture H Pacemaker works abnormally; check the pacemaker.
Pacemaker Not work H
H The patient ECG signal is too weak, and the system can’t
ECG Signal weak analyze. Check the patient's condition, electrodes, cables
and leads.
ST-I Too High ST value is higher than the upper alarm limit or lower
ST-I Too Low than the lower alarm limit. Check the patient’s
ST-II Too High physiological condition, and check if the patient category
M* and alarm limit settings are appropriate for the patient.
ST-II Too Low
ST-III Too High
ST-III Too Low

RR Too High Patient PR value is higher than the upper alarm limit or
lower than the lower alarm limit. Check the patient's
M*
RR Too Low physiological condition, and check if the patient category
Resp
The patient’s respiratory signal is too weak, and the
Apnea(RESP) H system can’t analyze. Check the patient's condition,
electrodes, cables and leads.
RESP ARTIFACT H* Respiration heartbeat interference
T1 Too High T1/T2 value is higher than the upper alarm limit or lower
T1 Too Low than the lower alarm limit. Check the patient's
T2 Too High physiological condition, and check if the patient category
T2 Too Low and alarm limit settings are appropriate for the patient.
Temp M*
TD value is higher than the upper alarm limit or lower
TD Too High
SpO2 Too High SpO2 value is higher than the upper alarm limit or lower
SpO2 Too Low physiological condition, and check if the patient category
SpO2 M*
PR Too High PR value is higher than the upper alarm limit or lower
PR Too Low physiological condition, and check if the patient category
NIBP signal weak NIBP value is higher than the upper alarm limit or lower
NIBP-Sys Too High than the lower alarm limit. Check the patient's
NIBP-Sys Too Low physiological condition, and check if the patient category
NIBP M* and alarm limit settings are appropriate for the patient.
NIBP-Mean Too High
NIBP-Mean Too Low
NIBP-Dia Too High
IBP Art-Sys Too High M* IBP value is higher than the upper alarm limit or lower
PA-Sys Too High than the lower alarm limit. Check the patient's
P1-Sys Too High physiological condition, and check if the patient category
P2-Sys Too High and alarm limit settings are appropriate for the patient.
Art-Dia Too High
PA-Dia Too High
P1-Dia Too High
P2-Dia Too High
Art-Mean Too High
PA-Mean Too High
CVP-Mean Too High
LAP-Mean Too High
RAP-Mean Too High
ICP-Mean Too High
P1-Mean Too High
P2-Mean Too High
CO2 EtCO2 Too High M* EtCO2 or FiCO2 or AWRR value is higher than the upper
EtCO2 Too Low alarm limit or lower than the lower alarm limit. Check the
FiCO2 Too High patient's physiological condition, and check if the patient
FiCO2 Too Low category and alarm limit settings are appropriate for the
AWRR Too High patient.
AWRR Too Low
H The patient’s respiratory signal is too weak, and the
APNEA(CO2) system can’t analyze. Check the patient's condition,
electrodes, cables and leads.
C.O. BT Too High M* BT value is higher than the upper alarm limit or lower
BT Too Low than the lower alarm limit. Check the patient's


C.O. Too High C.O. value is higher than the upper alarm limit or lower
C.O. Too Low than the lower alarm limit. Check the patient's
5.1.2 Technical Alarm Information

Connect to AC power supply, and charge the battery,
System Battery Low H and power with the battery as needed after fully
charged.
ECG ECG Comm. Stop H ECG module failure, or communication failure between
ECG Comm. Error H the module and the host; please restart the device.
ECG Config Error H
ECG Selfcheck Error H
ECG Lead Off M* The electrodes are not connected to the patient firmly or
ECG YY OFF (YY is a fall off, or lead wires and the main cable fall off. Check
M*
lead name) the connection of electrodes and lead wires.
TEMP1 Sensor Off L The temperature sensor falls off from the patient. Check
Temp
TEMP2 Sensor Off L the sensor connection.
SpO2 Comm. Stop H SpO2 module failure, or communication failure between
SpO2 Comm. Error H the module and the host; please restart the device.
SpO2 No Sensor L SpO2 sensor falls off from the patient or monitor,
SpO2 Sensor Off malfunctions, or sensor other than specified in this
L Manual is used. Check the sensor mounting position,
whether the sensor is damaged or sensor type.
SpO2 SpO2 Search Timeout L Reconnect the sensor or use new sensor.
SpO2 Search Pulse Sensor signal is poor or too weak. Check the patient's
condition, and place the sensor in a suitable position. If
L the failure persists, replace the sensor.
NIBP Comm. Stop H NIBP module failure, or communication failure between

NIBP Comm. Error H the module and the host; please restart the device.
NIBP Selfcheck error H
NIBP CFG Error H
NIBP system error H If failure occurs during measurement, the system can’t
NIBP analyze and calculate. Check the patient's condition,
Measurement timeout L check the connections or replace the cuff, and then re-
test.
The used cuff does not match the set patient category.
Cuff type error L Verify the patient category and replace the cuff.
NIBP cuff isn’t placed or connected properly, or there is

Cuff loose or no cuff L
gas leak.
Cuff leak L Check cuff and inflation tube.
Ambient atmospheric pressure is abnormal. Confirm that
the environment complies with the monitor's
Air pressure error L
specifications, and check whether there are special
NIBP
reasons affecting ambient pressure.
The measured blood pressure of the patient exceeds the
NIBP over range L
measuring range.
Patient’s pulse may be weak or cuff is too loose. Check
NIBP signal weak L the condition of the patient, and place the cuff in a
suitable position. If the failure persists, replace the cuff.


NIBP signal unstable Excessive movement may result in too much motion
artifact or interference in the signal during measurement.
L
NIBP signal saturated Motion signal amplitude is too large due to movement
L
and other reasons.
NIBP over pressure Cuff overpressure, and gas blockage may occur; check
L
the gas path, and then re-measure.
NIBP module reset error; check the gas path is blocked,
Module reset failed L
and then restart the measurement.
IBP IBP1&IBP2 Comm. Stop H IBP module failure, or communication failure between
IBP1 & IBP2 the module and the host; please restart the device.
H
Comm. Error
IBP1 Sensor Off L IBP sensor falls off from the patient or monitor,
malfunctions, or sensor other than specified in this
Manual is used. Check the sensor mounting position,
L
IBP2 Sensor Off Reconnect the sensor or use new sensor.
CO2 CO2 Comm. Stop H CO2 module failure, or communication failure between
the module and the host; please restart the device and
CO2 Comm. Error H
check the CO2 module.
Please check whether the CO2 sensor is connected well
CO2 Sensor Off H
with the host.
Replace O2 Sensor M please change another O2 sensor.
maybe there is something wrong with the adapter，
Check Adapter M
please check the adapter
maybe there is something wrong with the sampling line,
Check Sampling Line M
please check the sampling line
one param accuracy err M the accuracy of the parameter is error
Sensor Err(CO2) M the CO2 sensor is not match to the module
O2 calib required M please calibration the O2
Air calib required M please calibration the Air
Software Error(CO2) M the software of the CO2 is error
Hardware Error(CO2) M the hardware of the CO2 is error
Motor out of Motor out of accuracy
M
accuracy(CO2)
Factory Calibration please do the factory calibration
M
lost(CO2)
O2 Sensor Error M the O2 sensor is not match to the module
Replace Adapter M change another adapter
Sampling line clogged M please replace the sampling line
No Sampling line M please connect the sampling line
No Adapter M there is no adapter, please connect the adapter
O2 Port Error M the O2 port error, please check the O2 port
CO2 out of accuracy M CO2 out of accuracy
N2O out of accuracy M N2O out of accuracy
O2 out of accuracy M O2 out of accuracy
Temp out of Temp out of accuracy(CO2)
M
accuracy(CO2)
Pressure out of Pressure out of accuracy(CO2)
M
accuracy(CO2)
Zero required(CO2) M Perform zeroing operation
Me CO2 module is zeroing
CO2 is zeroing ssa
ge
CO2 is sleeping Me the mode is standby


ssa
ge
Span Calibrating(CO2) M the CO2 module is calibrating
Span Cal Error(CO2) M the CO2 module calibration error
C.O. C.O. BT Sensor Off L C.O. sensor falls off from the patient or monitor,
malfunctions, or sensor other than specified in this
Manual is used. Check the sensor mounting position,
Reconnect the sensor or use new sensor.
5.2 Machine malfunction

Malfunction phenomenon Possible reason Handle method
Boot without display and power ① Film key damaged ① Check adaptor and battery
indicator do not light. ② Adaptor not plugged in and ② Replace film key
the battery no power ③ Replace main control board
③ No electricity and battery
power
④ Main control board damaged
Boot no display or work in ① Main control board damaged ① Check display screen cable plug
black, but the power indicator ② Display screen damaged ② Replace display screen
light is on
One measurement function or ① Main control board and the ① Further check main control board
operation failure corresponding parts and the corresponding parts
damaged
Occasional crash ① Power grid instantaneous Re-boot is normal , if not normal, then
strong interference began to troubleshoot as follows：
② Poor adaptor performance ① Replace main control board
③ Poor main control board ② Replace power adaptor
performance
5.3 Operating & Recording

Button or Encoder failure ① Film key or Encoder ① Check the FPC cable in film key.
damaged ② Replace film key or encoder
② The cable which connected ③ Replace main control board
film key or encoder with
main control board damaged
③ Main control board damaged
Sound hoarse or failing ① Main control board damaged ① Replace main control board
② Speaker or connection cable ② Replace speaker or connection
damaged cable damaged

5.4 Power board and battery malfunction

Battery indicator don’t light ① Battery is damaged ① Change battery

when battery is charged ② Film key is damaged ② Change film key
③ Main control board is ③ Change main control board
damaged
Battery can’t be charged ① Battery is damaged ① Change battery
② Power adaptor is damaged ② Change power adaptor
③ Main control board is ③ Change main control board
damaged
5.5 Parameter malfunction

ECG waveform abnormalities ① Wrong electrode connection ① Connect measurement electrode
or interference way piece correctly
② Here is a floating electrode ② Remove unused electrode piece
piece ③ Choose the appropriate filter mode
③ Wrong ECG filter mode ④ Replace integrated parameter
selection board
④ Poor integrated parameter
board
No respiration waveform or ① Poor electrode connection ① Use the RL-LL electrode to make
respiration waveform ② Patient in frequent activities the connection position correct
abnormalities ③ Poor integrated parameter ② Keep patient silence
board ③ Replace integrated parameter
board
Temperature measurement ① Poor measurement sensor ① Connect and fix TEMP sensor
value is wrong connection ② Replace TEMP sensor
② TEMP sensor damaged ③ Replace integrated parameter
③ Poor integrated parameter board
board
Arrhythmia, arrhythmia and ① Poor ECG measurement ① Adjust the connection so that the
ST Segment analysis is waveform measurement waveform is
incorrect ② Poor integrated parameter normalReplace integrated
board parameter board
NIBP can not inflated ① Air way folding or leakage ① Check air way or Replace NIBP
② Poor integrated parameter cuff
board ② Replace integrated parameter
board
Occasionally undetectable ① NIPB cuff loose & patient ① Keep patient still and tied cuff
NIBP move ② Choose appropriate patient model
② Wrong patient mode selection
NIBP measurement error is ① Cuff size is not suitable for ① Choose appropriate NIBP cuff
big patient ② Choose appropriate patient model
② Wrong patient mode selection ③ Replace integrated parameter
③ Poor integrated parameter board
board
No SpO2 waveform ① SpO2 sensor damaged ① Replace new SpO2 sensor
② Not using original sensor or ② Check the sensor is compatible,
wrong sensor use try to use the original sensor
③ Poor integrated parameter ③ Replace integrated parameter
board board
SpO2 waveform have strong ① Patient in the activities ① Keep patient silence
interference ② Ambient light is too strong ② Weaken the surrounding ambient

③ SpO2 sensor did not folder light

good ③ Adjust sensor in right position
SpO2 measurement value ① Patient with a color injection ① Dye exclusion before measurement
inaccurate ② Patient’s finger coated with ② Clean up finger which will clip
sth. sensor
③ SpO2 sensor in wrong ③ Adjust sensor in right position
position

Service Telephone and Fax. Numbers

Telephone: +82 31 750 0340
Fax: +82 31 750 0344
Bistos Co., Ltd.

7th FL., A Bldg., Woolim Lions Valley 5-cha, 302, Galmachi-ro,
Jungwon-gu, Seongnam-si, Gyeonggi-do, Korea
www.bistos.co.kr
bistos@bistos.co.kr

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P/N : 770-ENG- SVM-EUR-D00 Bistos Co.,Ltd 2017, 11

Section 2 Introduction ∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙ 5

Section 3 Disassemble & Assemble ∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙ 11

Section 4 Maintenance & Conservation ∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙ 23

Section 5 Troubleshooting ∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙∙ 26

P/N : 770-ENG- SVM-EUR-D00 Bistos Co.,Ltd 2017, 11

WARNING Can lead to serious injury or death.

P/N : 770-ENG- SVM-EUR-D00 Bistos Co.,Ltd 2017, 11

1.2 General Precaution on Environment

Avoid placing in an area

Avoid placing in an area

Avoid placing in an area

Avoid placing in an area

Power off when the pulse

1.3 Definition of Symbols

Indicates DC power supply.

Indicates the packing material is recyclable.

Federal law restricts this device to sale by or on the order of a physician..

P/N : 770-ENG- SVM-EUR-D00 Bistos Co.,Ltd 2017, 11

(1) Parameter measurement part

2.1.1 Parameter measurement part

2.1.2 Main control part

2.1.3 Main – machine interface part

2.1.4 Power part

2.1.5 Auxiliary function part

P/N : 770-ENG- SVM-EUR-D00 Bistos Co.,Ltd 2017, 11

2.2 options and accessories

ECG cable and

Adult NIBP cuff

P/N : 770-ENG- SVM-EUR-D00 Bistos Co.,Ltd 2017, 11

2.3 Description of Product

2.3.1 Description of the BT-770 Front

6 To reset the alarm condition.

11 Freeze/unfreeze the waveform.

P/N : 770-ENG- SVM-EUR-D00 Bistos Co.,Ltd 2017, 11

2.3.2 Description of the BT-770 side

1 SpO2 SpO2 cable interface

P/N : 770-ENG- SVM-EUR-D00 Bistos Co.,Ltd 2017, 11

2.3.3 Description of the BT-770 Rear

3 Air outlet Heat dissipation

4 Battery cover Battery compartment cover

5 Bracket To wall mount the monitor

6 ID label Identify the monitor information

7 Air intake For ventilation

10 USB port For trend or software upgrade

11 Power adapter 15V, 2.4A adapter

P/N : 770-ENG- SVM-EUR-D00 Bistos Co.,Ltd 2017, 11

2.4 Product installation

2.4.1.1 Check the patient monitor

2.4.1.2 Start the patient monitor

2.4.1.3 Connect the sensors

2.4.1.4 Start monitoring

2.4.2 Turn off

P/N : 770-ENG- SVM-EUR-D00 Bistos Co.,Ltd 2017, 11