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SERVICE MANUAL
OMNI
Patient Monitor
Caution: Federal law (U.S.A.) restricts this device to sale by or on the order of a physician.
© 2011 Infinium Medical, Inc. All rights reserved. Ver 1.0, Issued date: Jan 25, 2011
Infinium Medical Inc.
Website: www.infiniummedical.com
Address: 12151 62nd St North #5
Largo Fl, 33773 USA
Toll Free (US call only): 866-918-8434
International: 1-727-531-8434
Fax: 1-727-531-8436
To obtain information about a warranty, if any, for this product, contact Infinium Medical Technical Services or your
local Infinium Medical representative.
TABLE OF CONTENTS
SECTION 1: INTRODUCTION ............................................................................................................... 4
1.1 MANUAL OVERVIEW ................................................................................................................... 4
1.2 WARNINGS, CAUTIONS AND NOTES .......................................................................................... 4
1.3 OMNI PATIENT MONITOR DESCRIPTION .................................................................................. 4
1.4 RELATED DOCUMENTS ............................................................................................................... 5
SECTION 2: INTRODUCTION AND SYSTEM DESCRIPTION .......................................................... 6

2.1 SYSTEM OVERVIEW ..................................................................................................................... 6
2.2 SYSTEM BLOCK DIAGRAM ......................................................................................................... 6
2.2.1 POWER SYSTEM .............................................................................................................. 7
2.2.1.1 PIN ASSIGNMENT AND DESCRIPTION FOR AC-DC MODULE .......................................... 8
2.2.1.2 PIN ASSIGNMENT AND DESCRIPTION FOR DC-DC MODULE .......................................... 9
2.2.1.3 DC-DC MODULE TEST POINTS..................................................................................... 11
2.2.2 MAINBOARD (ARM-FPGA SYSTEM，ERT MODULE（ECG, RESP, TEMP,SPO2）) .......... 11
2.2.2.1 PIN ASSIGNMENT AND DESCRIPTION FOR MAINBOARD .............................................. 12
2.2.2.2 MAINBOARD TEST POINTS........................................................................................... 14
2.2.2.3 FPGA ................................................................................................................................ 14
2.2.2.4 ARM (ADVANCED RISC MACHINE).................................................................................. 14
2.2.2.5 ERT MODULE（ECG, RESP, TEMP, SPO2） ................................................................... 15
2.2.3 NIBP MODULE ................................................................................................................. 16
2.2.3.1 PIN ASSIGNMENT AND DESCRIPTION FOR NIBP MODULE ............................... 19
2.2.4 SPO2 MODULE................................................................................................................ 19
2.2.5 DISPLAY ........................................................................................................................... 20
2.2.5.1 PIN ASSIGNMENT FOR TFT LCD PANEL DRIVING ............................................... 20
2.2.6 KEYBOARD (SWITCHES) .............................................................................................. 22
2.2.7 TOUCH PANEL ................................................................................................................ 22
2.2.8 SPEAKER ......................................................................................................................... 23
2.2.9 RECORDER ..................................................................................................................... 23
2.2.9.1 PIN ASSIGNMENT FOR RECORDER MODULE ...................................................... 25
2.2.10 RS-232 ............................................................................................................................ 26
SECTION 3: PERFORMANCE VERIFICATION................................................................................. 27

3.1 INTRODUCTION .......................................................................................................................... 27
3.2 EQUIPMENT NEEDED ................................................................................................................. 27
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Service Manual for OMNI
3.3 PERFORMANCE TESTS ............................................................................................................... 27
3.3.1 BATTERY CHARGE ........................................................................................................ 28
3.3.2 BATTERY PERFORMANCE TEST ................................................................................ 28
3.3.3 POWER-ON SELF-TEST ................................................................................................ 28
3.3.4 HARDWARE AND SOFTWARE TESTS ........................................................................ 29
3.3.5 OPERATION WITH A HUMAN SUBJECT ..................................................................... 30
3.4 SAFETY TESTS............................................................................................................................. 30
SECTION 4: ROUTINE MAINTENANCE ............................................................................................ 35

4.1 CLEANING.................................................................................................................................... 35
4.2 PERIODIC SAFETY AND FUNCTIONAL CHECKS ..................................................................... 35
4.3 BATTERY ..................................................................................................................................... 35
4.4 ENVIRONMENTAL PROTECTION.............................................................................................. 36
SECTION 5: DISASSEMBLY GUIDE.................................................................................................. 37

5.1 INTRODUCTION .......................................................................................................................... 37
5.2 HOW TO USE THIS SECTION ...................................................................................................... 38
5.3 DISASSEMBLY FLOW CHARTS ................................................................................................. 38
SECTION 6: PARTS ............................................................................................................................. 41

6.1 INTRODUCTION .......................................................................................................................... 41
SECTION 7: TROUBLESHOOTING.................................................................................................... 44
7.1 INTRODUCTION .......................................................................................................................... 44
7.2 HOW TO USE THIS SECTION ...................................................................................................... 44
7.3 WHO SHOULD PERFORM REPAIRS ........................................................................................... 44
7.4 REPLACEMENT LEVEL SUPPORTED ........................................................................................ 44
7.5 OBTAINING REPLACEMENT PARTS ......................................................................................... 44
7.6 TROUBLESHOOTING GUIDE...................................................................................................... 45
SECTION 8: PACKING FOR SHIPMENT ........................................................................................... 51

8.1 GENERAL INSTRUCTIONS ......................................................................................................... 51
8.2 REPACKING IN ORIGINAL CARTON ......................................................................................... 51
8.3 REPACKING IN A DIFFERENT CARTON ................................................................................... 51
SECTION 9: SPECIFICATIONS .......................................................................................................... 52
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List of Figures
FIGURE 2-1: OMNI SYSTEM BLOCK DIAGRAM .............................................................................. 7
FIGURE 2-2: POWER SYSTEM BLOCK DIAGRAM ............................................................................ 8
FIGURE 2-3: PIN ASSIGNMENT FOR AC-DC MODULE ..................................................................... 8
FIGURE 2-4: PIN ASSIGNMENT FOR DC-DC MODULE ..................................................................... 9
FIGURE 2-5: MAINBOARD BLOCK DIAGRAM ................................................................................. 12
FIGURE 2-6: PIN ASSIGNMENT FOR MAINBOARD .......................................................................... 12
FIGURE 2-7: ERT SYSTEM BLOCK DIAGRAM ............................................................................... 15
FIGURE 2-8: RESPIRATION SYSTEM BLOCK DIAGRAM ................................................................. 16
FIGURE 2-9: TEMPERATURE SYSTEM BLOCK DIAGRAM ............................................................... 16
FIGURE 2-10: NIBP SYSTEM BLOCK DIAGRAM ........................................................................... 17
FIGURE 2-11: OSCILLATORY CHARACTERISTICS DIAGRAM ........................................................... 18
FIGURE 2-12: PIN ASSIGNMENT FOR NIBP MODULE .................................................................... 19
FIGURE 2-13: SPO2 SYSTEM BLOCK DIAGRAM .......................................................................... 20
FIGURE 2-14: PIN ASSIGNMENT FOR KEYBOARD .......................................................................... 22
FIGURE 2-15: RECORDER MODULE BLOCK DIAGRAM .................................................................. 25
FIGURE 2-16: PIN ASSIGNMENT FOR RECORDER MODULE ........................................................... 25
FIGURE 2-17: RS232 PIN NO. DIAGRAM .................................................................................... 26
FIGURE 5-1: OMNI DISASSEMBLY SEQUENCE FLOW CHART, SHEET 1......................................... 38
FIGURE 5-2: OMNI DISASSEMBLY SEQUENCE FLOW CHART, SHEET 2......................................... 39
List of Tables
Table 2-1: RS-232 Serial Interface Connections…………………………………………………..26
Table 3-1: Required Test Equipment………………………………………………………………27
Table 3-2: Earth Leakage Current Values…………………………………………………………31
Table 3-3: Enclosure Leakage Current……………………………………………………………31
Table 3-4: Patient Leakage Current Values………………………………………………………32
Table 3-5: Patient Leakage Current Values— Mains Voltage on Applied Part………………33
Table 3-6: Test Lead Combinations…………………………………………………………………34
Table 3-7: Allowable Leakage Current………………………………………………………………34
Table 6-1: OMNI spare parts list……………………………………………………………………42
Table 6-2: OMNI Accessories………………………………………………………………………43
Table 7-1: Problem Categories………………………………………………………………………45
Table 7-2: Lists recommended actions to address power problems……………………………46
Table 7-3: Switches/Knob Problems…………………………………………………………………47
Table 7-4: Display/Audible Tones Problems…………………………………………………………47
Table 7-5: Operational Performance Problems………………………………………………………48
Table 7-6: Serviceable Hardware Error Messages…………………………………………………49
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SECTION 1: INTRODUCTION
1.1 MANUAL OVERVIEW
1.2 WARNINGS, CAUTIONS AND NOTES
1.3 OMNI PATIENT MONITOR DESCRIPTION
1.4 RELATED DOCUMENTS
1.1 MANUAL OVERVIEW
This manual contains information for servicing the model OMNI patient monitor,
throughout this manual. Only qualified service personnel should service this product.
Before servicing the OMNI, read the user’s manual carefully for a t horough
understanding of operation.
1.2 WARNINGS, CAUTIONS AND NOTES
This manual uses two terms that are important for proper operation of the monitor:
Warning, Caution, and Note.
1.2.1 Warning
A warning precedes an action that may result in injury or death to the patient or user.
1.2.2 Caution
A caution precedes an action that may result in damage to, or malfunction of, the monitor.
Cautions are highlighted in boldface type.
1.2.3 Note
A note gives information that requires special attention.
1.3 OMNI PATIENT MONITOR DESCRIPTION
The OMNI monitor is a c omprehensive monitoring system with two or three traces
compiling, processing, analyzing and displaying data from up to eight different patient
parameters. It integrates parameter measuring modules, display and recorder in one
device, featuring in compactness, lightweight and p ortability. Built-in battery facilitates
transportation of patient.
The purpose and function of the OMNI monitor is to monitor ECG, heart rate, NIBP
(systolic, diastolic, and mean arterial pressures), SpO2, respiration, temperature, and
EtCO2 for adult, neonate and pediatric patients in all hospital areas and hospital-type
facilities. It may be used during hospital transport and in mobile, land-based environments,
such as ambulances.
The OMNI monitor offers advanced features such as an intuitive touchscreen with clinical
measurements, one-touch commands, crisp and clear display.
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The physical and operational characteristics of the monitor are described in the user’s
manual and in the Specifications section of this manual.
1.4 RELATED DOCUMENTS
To perform test and troubleshooting procedures and to understand the principles of

operation and circuit analysis sections of this manual, you must know how to operate the
monitor. Refer to the OMNI user’s manual. To understand the various sensors, ECG leads,
blood pressure cuffs, SPO2 probe and etc. that work with the monitor, refer to the
individual directions for use that accompany these accessories.
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SECTION 2: INTRODUCTION AND SYSTEM DESCRIPTION
2.1 SYSTEM OVERVIEW
2.2 SYSTEM BLOCK DIAGRAM
2.2.1 POWER SYSTEM
2.2.2 MAINBOARD (ARM-FPGA SYSTEM，ERT MODULE（ECG, RESP, TEMP,SPO2）)
2.2.3 NIBP MODULE
2.2.4 SPO2 MODULE
2.2.5 DISPLAY
2.2.6 KEYBOARD (SWITCHES)
2.2.7 TOUCH PANEL
2.2.8 SPEAKER
2.2.9 RECORDER
2.2.10 RS-232
2.1 SYSTEM OVERVIEW
2.1.1 The Complete OMNI Patient Monitor System

The OMNI patient monitor is a full-function monitor for use on adult, notate and pediatric
patients. The functions performed by the system include monitoring patient ECG, heart
rate, respiration rate, non-invasive blood pressures, blood oxygen saturation, ETCO2 and
dual temperature.
In addition to monitoring and displaying the status of these physiological parameters, the
instrument performs various microprocessor-programmed analytical functions, such as:
 Creating both visual and audible alarm signals when settable limits are violated;
  C re a ting a nd dis pla ying wa rning m e s s a ge s whe n conditions a re de te cte d tha t
would degrade or prevent valid measurements;
 Creating and displaying trend waveforms or tabular data;
  P roviding input to a n optiona l re corde r forprintout of current or trend waveforms
or tabular data.
The monitor is essentially a b attery-powered instrument. An internal charging unit is

designed to accept only an AC line voltage.
The charger uses these external power sources to maintain a “ float” voltage source
available from the batteries.
2.2 SYSTEM BLOCK DIAGRAM
The OMNI patient monitor functions are represented graphically in the System Block
Diagram, Figure 2-1. Each section of the System Block Diagram is described briefly in the
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text that follows the illustration. This is followed by more detailed descriptions of the theory
of operation of each block.
NIBP
Patient Connectors
Module
SpO2
ECG TEMP
Module
Power
AC Input Main Board
Supply
Lithium-Ion
Battery
External Keypad
RS232 SPEAKER
Interface Switches
FIGURE 2-1: OMNI SYSTEM BLOCK DIAGRAM
2.2.1 POWER SYSTEM
The power system section contains a power supply capable of operating the monitor and
charging the battery from either an AC source of 100 to 240 volts at 50 to 60 Hz or 16.7
volt DC input. This section also contains the battery, battery monitoring circuitry, and
battery charging circuitry. The battery provides the operating power for the monitor. Power
system outputs of +5 volts DC, +8.3 volts DC, and +12 volts DC are developed for use
throughout the non-isolated portions of the monitor. The power system is illustrated in the
diagram below.
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FIGURE 2-2: POWER SYSTEM BLOCK DIAGRAM
2.2.1.1 PIN ASSIGNMENT AND DESCRIPTION FOR AC-DC MODULE
CN1
1
CN2
2
1
3
2
TRANSFORMER
CAPACITOR
FIGURE 2-3: PIN ASSIGNMENT FOR AC-DC MODULE
Port CN1：
Pin Description
1 AC 220V input
2 not connected
3 AC 220V input
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Port CN2：
Pin Description
1 Ground
2 Ground
3 DCX, output +16.8vdc for DC/DC module
4 not connected
2.2.1.2 PIN ASSIGNMENT AND DESCRIPTION FOR DC-DC MODULE
FLY2
DC
BAT
1 CONTROL
1 ASPO2 1 NET 1 NBP 1 PRINTPOW
FIGURE 2-4: PIN ASSIGNMENT FOR DC-DC MODULE
ASPO2:（Communicate with SPO2 module）

1 SPO2TXD, external spo2 module data output
2 Ground
3 Ground
4 DVCC, +5vdc for external spo2 module
NET：(To RS232 Interface)

Pin Description
1 DVCC , +5vdc for external RS232 interface
2 Ground
3 RXD, external RS232 interface
4 TXD, external RS232 interface
CONTROL:（Communicate with mainboard）

Pin Description
1 DVCC, +5vdc for mainboard power supply
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4 DVCC , +5vdc for mainboard power supply

5 Ground
6 Ground
7 Ground
8 Ground
9 POWKEY, power key signal input
11 POWDOWN, power down signal
12 NBPRXD, RS232 interface of NIBP
13 DCIN, +16.1vdc for power supply mode detecting
14 NBPTXD, RS232 interface of NIBP
15 Ground
17 Ground
19 Ground
20 PRINTRXD, RS232 interface of PRINTER
21 Ground
22 PRINTTXD, RS232 interface of PRINTER
23 OCOUT, battery charging signal
24 POWLED, AC LED control
NBP：（To NIBP module）

Pin Description
3 +12vdc for NIBP power supply
4 Ground
5 Ground
6 +12vdc
PRINTPOW：（To recorder module）

Pin Description
1 +8.3vdc for PRINTER power supply
2 +8.3vdc for PRINTER power supply
3 Ground
4 Ground
7 Ground
BAT：（To battery）
Pin Description
1 BATT, battery input
2 Ground
3 Ground
DC：（To AC/DC module）

Pin Description
1 DCX, +16.8vdc for DC/DC module
2 Ground
FLY2：(To fan connector)

1 Ground
2 FANPOW, +12vdc for fan
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2.2.1.3 DC-DC MODULE TEST POINTS
Location Function
E1 Negative lead Primary Ground
Measure U2 pin 2 72KHz Drive frequency
C6 Positive lead +16.8vdc output
C8 Positive lead +5vdc output
C15 Positive lead +8.3vdc output
C11 Positive lead +12vdc output
2.2.2 MAINBOARD (ARM-FPGA SYSTEM，ERT MODULE（ECG, RESP, TEMP,SPO2）)
The OMNI main control system adopts control kernels including 32-bit 96 MHz ARM9E
based MCU microcontroller and FPGA. The design is modularization. All functional
modules communicate each other by the standard UART（Serial）.
The ARM microcontroller completes functions of management of modules,

human-machine interface, data I/O management, system application software, ports
management and project, etc.
The FPGA has display drive, graphic display and waveform display functions. It has an
advanced multi-layer graphs and waveforms display technology; each waveform occupies
an individual graphic layer. So there is no influence among waveforms and texts. There
will have high display efficiency. The programming work will become be simple. The CPU
workload will be reduced.
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To To
Power NIBP
Module Module
RTC/ E2 PROM
SpO2
ECG CPU
Touch
ETCO2 Screen
module
Serial User Indicator

Interface
FPGA
Interface LEDs
Speaker
FIGURE 2-5: MAINBOARD BLOCK DIAGRAM
2.2.2.1 PIN ASSIGNMENT AND DESCRIPTION FOR MAINBOARD
FIGURE 2-6: PIN ASSIGNMENT FOR MAINBOARD
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LED：
Pin Description
1 GND, Ground
2 LED2, DC LED control
3 LED1, AC LED control
4 POWKEY, POWKEY control
5 POWLED, control POWKEY LED
QTEMP：
Pin Description
1 DVCC +5vdc output for fast temperature module
2 RX receive data from fast temperature module
3 TX transit data to fast temperature module
4 DGND ground
ETCO2：
Pin Description
1 DVCC, +5vdc for ETCO2 module power supply
2 Ground
3 Ground
4 DVCC, +5vdc for ETCO2 module power supply
5 TX232CO2, RS232 interface of ETCO2
6 RX232CO2, RS232 interface of ETCO2
7 Ground
8 Ground
CONTROL:（communicate with Mainboard）

Pin Description
5 Ground
6 Ground
7 Ground
8 Ground
9 POWKEY, power key signal input
11 POWDOWN, power down signal
13 DCIN, +16.1vdc for power supply mode detecting
15 Ground
17 Ground
19 Ground
21 Ground
23 OCOUT, battery charging signal
24 POWLED, AC LED control
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2.2.2.2 MAINBOARD TEST POINTS
Location Function
CF77 Negative lead Primary Ground
CF77 Positive lead +3.3vdc output
E9 Positive lead +2.5vdc output
E6 Negative lead Second Ground

E6 Positive lead +5vdc output
E7 Negative lead -5vdc output
E8 Positive lead +3.3vdc output
2.2.2.3 FPGA
A field-programmable gate array (FPGA) is a large-scale integrated circuit that can be

programmed after it is manufactured rather than being limited to a p redetermined,
unchangeable hardware function. The term "field-programmable" refers to the ability to
change the operation of the device "in the field," while "gate array" is a somewhat dated
reference to the basic internal architecture that makes this after-the-fact reprogramming
possible.
The CycloneTM field programmable gate array family is based on a 1.5-V, 0.13nm,
all-layer copper SRAM process, with densities up to 20,060 logic elements (LEs) and up
to 288 Kbits of RAM. With features like phaselockedloops (PLLs) for clocking and a
dedicated double data rate (DDR)interface to meet DDR SDRAM and f ast cycle RAM
(FCRAM) memory requirements.
2.2.2.4 ARM (ADVANCED RISC MACHINE)
STR912FA is a ARM-powered microcontroller which combines a 16/32-bit ARM966E-S

RISC processor core, dual-bank Flash memory, large SRAM for data or code, and a rich
peripheral set to form an ideal embedded controller for a wide variety of applications such
as point-of- ale terminals, industrial automation, security and surveillance, vending
machines, communication gateways, serial protocol conversion, and medical equipment.
The ARM966E-S core can perform single-cycle DSP instructions, good for speech
processing, audio algorithms, and low-end imaging.
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2.2.2.5 ERT MODULE（ECG, RESP, TEMP, SPO2）
2.2.2.5.1 OVERVIEW
The OMNI ERT module consists of eight major blocks: interface circuit, ECG, respiration,
temperature, controls, isolation, and A/D converter on the non-isolated side.
The instrument incorporates the standard ECG 3-lead or 5-lead system (I, II, III) . It
provides two levels of low frequency noise filtering, T-wave filtering, R-wave detection,
pacer detection capability and baseline reset. The abbreviations RA, LA, and LL are the
right arm, left arm, and left leg leads, respectively, and I, II, III are the potential differences
between the limbs.
An expanded block diagram of the ERT system is presented in the Figure 9-3.
FIGURE 2-7: ERT SYSTEM BLOCK DIAGRAM
2.2.2.5.2 ECG PROCESSING
The technique used in ECG senses the varying potential difference between two points at
the skin surface that respond to the chemical actions of the muscular activity of the heart.
Three electrodes are attached to the patient’s right arm (RA), left arm (LA) and left leg (LL).
The varying potentials at these locations are cable-connected to the ECG circuit inputs
where they are conditioned, and the difference of potential between two selected leads is
digitized before transmitting through opto-isolators to the processor. The
processor-installed algorithms operate on the signals to develop drivers for the graphic
display and to compute the heart rate in beats per minute (bpm).
In addition to the acquisition of the QRS waveform complex, the ECG input and
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subsequent signal processing computing circuitry perform a number of other functions:

· They detect a “lead-off” condition if one of the electrode connections is disrupted.
· They detect the presence of pacemaker signals within the QRS waveform complex of
the ECG.
2.2.2.5.3 RESPIRATION PROCESSING
The patient’s respiration is detected by using two (RA and L L) of the three leads of the
ECG electrodes and cable. A low-level excitation signal is applied to these leads, and the
variation of the thoracic impedance caused by the breathing is sensed and processed for
display and measurement.
FIGURE 2-8: RESPIRATION SYSTEM BLOCK DIAGRAM

2.2.2.5.4 TEMPERATURE PROCESSING
Measurement of patient temperature is accomplished by processing the signal from a
probe containing a r esistor whose impedance is temperature dependent. The class of
such components is called thermistor.
The OMNI patient monitor is designed to accept the signals from electrically isolated
Series YSI probes manufactured by Yellow Springs Incorporated. Interchangeable probes
in this series may be used for esophageal, rectal, skin or surface, or airway temperature
measurement. The signal from the probe is conditioned by the monitor input circuitry,
processed, and used to drive the numeric display.
FIGURE 2-9: TEMPERATURE SYSTEM BLOCK DIAGRAM
2.2.3 NIBP MODULE
The OMNI noninvasive blood pressure (NIBP) measurement and display operations
described in this section include the pneumatics of the inflatable cuff and control valves.
The NIBP section contains the pumps, valves, pressure measurement circuitry, and
control circuitry for the noninvasive blood pressure measurement. Pressure data is
converted to digital format and conveyed to the processor section.
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Prior to making blood pressure measurements, the cuff is placed around a limb, typically
an upper arm (left or right). The NIBP measurement system is initiated by commands
responding to pressing the NIBP Start/Stop switch on the front panel. The cuff is inflated
at a rate controlled by the pump excitation current to a pressure above systolic, at which
level the artery is effectively occluded. Then, as the cuff pressure is reduced at constant
rate, the pressure transducers provide analog signals to the digital hardware where they
are digitized and processed to obtain systolic, diastolic, and mean blood pressure values,
as well as the beat rate.
The technique for translating the pressure signals into the required measurements makes
use of the action of the oscillatory characteristic of the returning arterial pressure. The
phenomenon is illustrated in the diagram below.
Cuff Pump Valve_1 Valve_2
Pressure Pressure drive drive drive

Transducers_1 Transducers_2
Power NBP_MCU RS232
FIGURE 2-10: NIBP SYSTEM BLOCK DIAGRAM

See Figure 2-11. Systolic pressure is defined as the point at which oscillation increases
sharply. As the cuff deflates, oscillation amplitude increases to a maximum, and t hen
decreases. The point of peak oscillation amplitude is the mean arterial pressure. The point
at which oscillations cease is defined as the diastolic pressure.
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FIGURE 2-11: OSCILLATORY CHARACTERISTICS DIAGRAM
WARNING：
 The width of the cuff should be either 40% of the limb circumference (50% for
neonates) or 2/3 of the upper arm length. The inflatable part of the cuff should be
long enough to encircle 50-80% of the limb. The wrong size of cuff can cause
erroneous readings. If the cuff size is in question, then use a larger cuff.
 Make sure that the cuff edge falls within the range of 〈-〉. If does not, change a
more suitable cuff.
 Connect the cuff to the air hose. The limb chosen for taking the measurement
should be placed at the same level as the patient’s heart. If this is not possible you
should apply the following corrections to the measured values:
If the cuff is placed higher than the heart level, add 0.9mmHg (0.12kPa) for each
inch of difference.
If it is placed lower than the heart level, deduct 0.9mmHg (0.12kPa) for each inch of
difference.
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2.2.3.1 PIN ASSIGNMENT AND DESCRIPTION FOR NIBP MODULE
MCU
1 JOUT
FIGURE 2-12: PIN ASSIGNMENT FOR NIBP MODULE

JOUT：
Pin Description
1 TXD, RS232 interface of NIBP
2 RXD, RS232 interface of NIBP
3 +12vdc from DC/DC module
4 Ground
5 Ground
6 +12vdc from DC/DC module
2.2.4 SPO2 MODULE
See Figure 2-13. The OMNI contains a s aturated blood oxygen measurement module
using pulse oximetry techniques for noninvasive monitoring. The SpO 2 section is a
separate minisystem with its own analog section, A/D converter and microprocessor.
The Oximeter determines %SpO2 and pulse rate by passing two wavelengths of light, one
red (660nm, 2.0mW) and one infrared (905nm, 2.0-2.4mW), through body tissue to a
photo detector.
During measurement, the signal strength resulting from each light source depends on the
color and thickness of the body tissue, the sensor placement, the intensity of the light
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sources, and the absorption of the arterial and venous blood (including the time varying
effects of the pulse) in the body tissues. The Oximeter processes these signals,
separating the time invariant parameters (tissue thickness, skin color, light intensity, and
venous blood) from the time variant parameters (arterial volume and %SpO2) to identify
the pulse rate and c alculate oxygen saturation. Oxygen saturation calculations can be
performed because oxygen saturated blood predictably absorbs less red light than oxygen
depleted blood.
SPO2 Amplifier RS232

MCU
Sensor
Power
FIGURE 2-13: SPO2 SYSTEM BLOCK DIAGRAM
2.2.5 DISPLAY
This module is a color active LCD module incorporating amorphous silicon TFT (Thin Tilm
Transistor). It is composed of a color TFL-LCD panel ICs, control circuit and power supply
circuit and a backlight unit. Graphics and texts can be displayed on a 800 X 3 X 480 dots
panel with 262,144 colors by using LVDS(Low Voltage Differential Signaling) system for
interface and supplying +3.3V and +5.0V DC supply voltage for TET-LCD panel driving
and supply voltage for backlight.
The TFT-LCD panel used for this module is low-reflection and higher-color-saturation
type.
Therefore, this module is also suitable for the multimedia use. Viewing angle is 6 o’clock
direction.
This module is the type of wide viewing angle and hi gh brightness (370cd/m2).
Backlight-driving DV/AC inverter is not built this module.
2.2.5.1 PIN ASSIGNMENT FOR TFT LCD PANEL DRIVING
Pin Description
1 Power for LED driver
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2 Power for LED driver

3 Adjust the LED brightness with PWM Pulse
4 Ground for LED circuit
5 Ground for LED circuit
6 Power for digital circuit
7 Power for digital circuit
8 DE or HV mode control Note 3
9 Data enable
10 Vsync signal input
11 Hsync signal input
12 Power ground
13 Blue data input (MSB)
14 Blue data input
15 Blue data input
16 Power ground
17 Blue data input
18 Blue data input
19 Blue data input(LSB)
20 Power ground
21 Green data input(MSB)
22 Green data input
23 Green data input
24 Power ground
25 Green data input
26 Green data input
27 Green data input(LSB)
28 Power ground
29 Red data input(MSB)
30 Red data input
31 Red data input
32 Power ground
33 Red data input
34 Red data input
35 Red data input(LSB)
36 Power ground
37 Sample clock
38 Power ground
39 Select left or right scanning direction Note 4,5
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40 Select up or down scanning direction
2.2.6 KEYBOARD (SWITCHES)
The keyboard circuit contains touch panel control and two red LEDs(AC Indicator and DC
indicator). The LEDs are driven by the power supply system. The keyboard system is
illustrated in the pins below.
PKEY 1
FIGURE 2-14: PIN ASSIGNMENT FOR KEYBOARD

PKEY:
Pin Description
6 GND, Ground
7 LED2, DC LED control
8 LED1, AC LED control
9 POWKEY, POWKEY control
10 POWLED, control POWKEY LED
The power switch, connected directly to the supply, toggles the power between Standby
and On modes. When in Standby, the display is blank, and n o monitoring is performed.
However, the batteries are charging if an AC power source is connected to the rear panel.
2.2.7 TOUCH PANEL
This touch panel belongs to Four-Wire analog resistive touch panel for normal operating
with 1,000,000~2,000,000 touching times.
It is with high transparency (more than 76%).It is quite clear even the monitor with low
brightness.
Use a plastic stylus (tip R0.8 or over) or finger to operate. Sharp edged or hard articles are
prohibited. The gathering of dew in the panel may occur with abrupt temperature or
humidity changes. A stable environment condition is recommended.
It consists of a conductive bottom layer (ITO Glass or Film) and a conductive top layer
(ITO Film).
The two layers are suspended by many very small spacer dots. When a certain point is
touched, the top layer contacts the bottom layer and a voltage charged by the controller is
- 22 -
applied to the bottom layer's electrodes.
The coordinate X axis of the touch point can be detected by measuring the voltage value
thru the top ITO layer and the coordinate Y axis of the touch point can be detected in the
same way by changing voltage input to the top layer's electrodes.
Capacitive Touch Screen Technology provides accurate and sensitive response to the
user's touch while offering outstanding durability. This type of touch screen technology
offers durability in the form of scratch resistance and contaminant resistance. Dirt, liquids,
and harsh chemicals have no ill effect on Capacitive Touch Screen Technology.
Capacitive Touch Screen Technology utilizes a g lass panel with a c apacitive (charge
storing) material coating its surface. Circuits located on the screen corners measure the
capacitance when the overlay experiences a t ouch. Screen technology measures the
frequency changes to determine the X/Y coordinates of the command, giving fast and
accurate results. This type of touch screen technology can use a thin, sleek design and
robust characteristics for touch; screen technology limitations, however, make it
necessary to use only a finger, not a stylus.
2.2.7.2 Pin Assignment for Touch Screen Panel
Pin Description
1 Top electrode – differential analog
2 Right electrode – differential analog
3 Bottom electrode – differential analog
4 Left electrode – differential analog
2.2.8 SPEAKER
The speaker is capable of providing 73 dBA of volume at a distance of one meter during
alarm conditions. The processor drives the speaker in different patterns as specified for
the different alarm priorities and conditions.
2.2.9 RECORDER
The optional recorder module is installed in the right panel of the monitor. It provides users
with the capability to obtain hard-copy records of selected vital signs information. Basic
control of the recorder is implemented by two push-switch controls on the recorder front
panel. One of these is used to obtain continuous recordings of the real-time waveforms
- 23 -
displayed in two graphic frames. Along with the waveforms, the recorder prints the values
of the vital signs being displayed.
If scrolling is enabled in a display frame containing trend data when the Knob switch is
operated, then the trend record for that vital sign is printed.
Recording is accomplished on 50 -mm wide thermal paper at recorder speeds

programmable up to 50 mm/sec.
- 24 -
Paper
Detector
CPU
UART
User Interface
Thermal
Printer
Motor Drive Motor
FIGURE 2-15: RECORDER MODULE BLOCK DIAGRAM
2.2.9.1 PIN ASSIGNMENT FOR RECORDER MODULE
MCU
POW 1 SIO 1
FIGURE 2-16: PIN ASSIGNMENT FOR RECORDER MODULE

POW：
Pin Description
1 Ground
2 Ground
3 +8.3vdc from DC/DC module
4 +8.3vdc from DC/DC module
SIO：
Pin Description
1 Ground
2 RXD, RS232 interface of PRINTER
3 TXD, RS232 interface of PRINTER
- 25 -
2.2.10 RS-232
2.2.10.1 OVERVIEW
This is a rear panel 9-pin connector providing interfaces with other computer systems or
equipment. The driver for this port is a Universal Asynchronous Receive-Transmit (UART)
integrated circuit that interfaces this port with the microprocessor. The baud rate for this
serial transmission function is 57600 baud.
Patient data can be obtained through the RS-232 I/O connector on the rear panel of the
monitor by connecting it to an attached PC.
2.2.10.2 CABLE CONNECTION

The 9-pin connector mounted on the rear panel provides an access port for a serial
(RS-232) interface to a suitably configured personal computer. Its pins layout is seen as
following picture:
FIGURE 2-17: RS232 PIN NO. DIAGRAM
Table 2-1: RS-232 Serial Interface Connections

Pin # Signal Definition
1 not used
2 TXD Transmit Data
3 RXD Received Data
4 not used
5 GND Signal Ground
6 not used
7 not used
8 not used
9 +5V Power Supply
- 26 -
SECTION 3: PERFORMANCE VERIFICATION
3.1 INTRODUCTION
This section discusses the tests used to verify performance following repairs or during
routine maintenance. All tests can be performed without removing the OMNI covers.
If the OMNI fails to perform as specified in any test, repairs must correct the problem before
the monitor is returned to the user.
WARNING: Do not place the OMNI into operation after repair or maintenance has
been performed, until all Performance Tests have been performed. Failure to
perform all tests could result in erroneous monitor readings.
3.2 EQUIPMENT NEEDED
Table 3-1: Required Test Equipment

Equipment Description
Digital multimeter
Multi-parameter simulator medSim 300B or equivalent
SPO2 simulator INDEX 2LF or equivalent
NIBP simulator Fluke BP Pump2, Cufflink
Temperature simulator THCY-15 or equivalent
Safety analyzer CS2675F, C2670Y,
CS2678 or equivalent
Interactive Biomedical Universal Signal iBUSS or equivalent
Sources
3.3 PERFORMANCE TESTS
The battery charge and b attery performance test should be performed before monitor
repairs whenever the battery is suspected as being a source of the problems. All other tests
may be used following repairs or during routine maintenance (if required by your local
institution. Before performing the battery performance test, ensure that the battery is fully
charged (Paragraph 3.3.1).
This section is written using Infinium Medical factory-set power-up defaults. If your
institution has preconfigured custom defaults, those values will be displayed.
- 27 -
3.3.1 BATTERY CHARGE
Perform the following procedure to fully charge the battery.

1. Connect monitor to AC power source using proper power cord.
2. Verify AC icon is displayed. AC SOURCE indicator is lit.
3. Charge the battery for at least 4 hours.
Note: The battery may require a complete charge/discharge cycle to restore its normal
capacity, depending on its previous usage.
4. The only way to check for a f ull charge is to perform the procedure in paragraph 3.2.2
“Battery Performance Test.”
3.3.2 BATTERY PERFORMANCE TEST
1. The OMNI monitor is specified to typically operate on battery power about 60 minutes
with no printing, and one NIBP measurement every 15 minutes. Before performing this test,
ensure that the battery is fully charged (paragraph 3.3.1).
2. Connect all cables and leads.
3. Set NIBP simulator to simulate pressure setting of 120/80 mmHg and set ECG simulator
to simulate heart rate of 80 bpm.
4. Ensure monitor is not connected to AC power.
7. With OMNI turned off, press On/Standby switch and verify battery icon appears at top of
display and battery indicator is lit after power-on self-test is completed. Boxes in battery
icon should all be filled, indicating battery is charged.
8. Verify monitor is responding to SPO2 simulator signal and audi ble alarm is sounding.
Use knob to select SPO2 Setup menu and permanently silence SPO2 audible alarm.
9. Use knob to select NIBP Setup menu and s et Automatic Measurement Interval to 15
minutes. Exit menu and press front panel NIBP Start/Stop switch to manually initiate first
NIBP measurement. Subsequent NIBP measurements will be taken automatically every 15
minutes.
10. OMNI monitor must operate for at least 60 minutes before monitor automatically powers
down due to low battery condition.
11. Verify low battery alarm occurs when represents the 25% electric energy of the battery
before battery fully discharges.
12. Allow monitor to operate until it automatically powers down due to low battery condition.
Press Alarm Silence switch to terminate this audible alarm.
13. If monitor passes this test, immediately recharge battery (paragraph 3.3.1, steps 1–3).
3.3.3 POWER-ON SELF-TEST
1. Connect monitor to AC power source and verify AC SOURCE indicator is lit.
- 28 -
2. Do not connect any input cables to monitor.

3. Observe the monitor front panel. With the monitor off, press the STANDBY/ON button.
The display backlight illuminates, but display is blank. The INFINIUM logo then appears for
a few seconds, with monitor type, version numbers of boot and operational software will
displayed in centre of display.
Note: Power-on self-test takes approximately 4 seconds to complete.

a. Upon successful completion of power-on self-test, display will be in normal monitoring
screen configuration.
b. No vital signs numeric values or waveforms will be displayed.
3.3.4 HARDWARE AND SOFTWARE TESTS
3.3.4.1 Power Supply Source Test
This procedure uses normal system components to test circuit operation. The power supply
source LED is used to indicate the power supply source type (battery or AC).
1. Connect an AC power cable to the socket on the rear panel of the monitor, press the
ON/STANDBY button to turn the monitor on. If AC SOURCE indicator is lit with green,
which means the AC SOURCE LED can work normally.
2. Power off the monitor. Unplug an AC power cable from the socket of the rear panel for
monitor, insert a charged batteries into battery housing (notice insertion direction, refer to
user’s manual, see its insert indication labeling on the battery), press the ON/STANDBY
button to turn the monitor on. If DC SOURCE indicator is lit with green, which means the DC
SOURCE LED can work normally. And the monitor works by battery.
3. Leave the sensor open with the LED and photo detector visible.
4. After the monitor completes its normal power-up sequence, verify that the sensor LED is
brightly lit.
3.3.4.2 Speaker Test
Press the ON/STANDBY button to turn the monitor on. After the normal power-up sequence,
click the screen, the speaker should sound. Press the ALARM SILENCE button on the front
panel of the monitor. The speaker is temporarily silenced.
3.3.4.3 Cooling Fan Test
Connect an AC power cable to the socket on the rear panel of the monitor and press the
ON/STANDBY button to turn the monitor on. If the cooling fan on the rear panel of the
monitor works with rotating and sounds a hum, that means the cooling fan works normally.
- 29 -
3.3.5 OPERATION WITH A HUMAN SUBJECT
Patient monitoring involves connecting the monitor to a human subject for a qualitative test.
1. Connect all cables, leads, electrodes, blood pressure hose, blood pressure cuff and
sensors to monitor according to directions for use.
2. Clip the oxygen probe to subject as recommended in sensor directions for use.
3. Apply appropriate subject according to the cuff directions for use.
4. Press On/Standby switch to turn monitor on and verify monitor is operating.
5. Monitor should stabilize on subject’s physiological signal in about 15 to 30 seconds.
6. Verify oxygen saturation, heart and respiration rates are reasonable for subject.
7. Press NIBP Start/Stop switch on front panel of monitor.
8. Verify that blood pressure values are reasonable for subject.
3.4 SAFETY TESTS
OMNI safety tests meet the standards of, and are performed in accordance with, IEC 601-1
for instruments classified as Class I and TYPE CF and BF.
3.4.1 Protective Earth Continuity

This test checks the integrity of the power cord ground wire from the AC plug to the
instrument chassis ground. The current used for this test is less than or equal to 6 Volts
RMS, 50 to 60 Hz, and 25 Amperes.
1. Connect the monitor AC mains plug to the analyzer as recommended by the analyzer
operating instructions.
2. Connect the analyzer resistance input lead to the equipotent terminal (ground lug) on the
rear of the instrument. Verify that the analyzer indicates 100 milliohms or less.
3.4.2 Electrical Leakage

The following tests verify the electrical leakage of the monitor:
· 3.4.2.1 Earth Leakage Current
· 3.4.2.2 Enclosure Leakage Current
· 3.4.2.3 Patient Leakage Current
· 3.4.2.4 Patient Source Current (Mains on Applied Part)
· 3.4.2.5 Patient Auxiliary Current
3.4.2.1 Earth Leakage Current

This test is in compliance with IEC 601-1 (earth Leakage current). The applied voltage for
IEC 601-1 the voltage is 264 Volts AC, 50 to 60 Hz. All measurements shall be made with
the power switch in both “On” and “Off” positions.
1. Connect the monitor AC plug to the electrical safety analyzer as recommended by the
- 30 -
analyzer operating instructions.

2. Perform test as recommended by analyzer operating instructions.
Note: Earth leakage current is measured under various conditions of the AC mains and
protective earth conductor. For each condition, the measured leakage current must not
exceed that indicated in Table 3-2.
Table 3-2: Earth Leakage Current Values
Test Condition Allowable Leakage
Current (microamps)
N.C. 500
S.F.C. 1000
N.C.：Normal Condition
S.F.C.: Single Fault Condition
3.4.2.2 Enclosure Leakage Current

This test is in compliance with IEC 601-1 (enclosure leakage current). This test is for
ungrounded enclosure current, measured between enclosure parts and earth. The applied
voltage for IEC 601-1 the applied voltage is 264 Volts AC at 50 to 60 Hz.
1. Connect the monitor AC plug to the electrical safety analyzer as recommended by the
2. Place a 200 cm 2 foil in contact with the instrument case making sure the foil is not in
contact with any metal parts of the enclosure that may be grounded.
3. Measure the leakage current between the foil and earth.
Note: The analyzer leakage current indication must note exceed the values listed in Table
3-4.
Table 3-3: Enclosure Leakage Current
Current (microamps)
N.C. 100
S.F.C. 500
3.4.2.3 Patient Leakage Current

This test measures patient leakage current in accordance with IEC 601-1, clause 19, for
Class I, type CF equipment. Patient leakage current in this test is measured from any
individual patient connection to earth (power ground).
1. Configure the electrical safety analyzer as recommended by the analyzer operating
instructions.
2. Connect the monitor’s AC mains power cord to the analyzer as recommended by the
3. Connect the ECG test cable between the ECG connector on t he OMNI and the
appropriate input connector on the analyzer.
- 31 -
4. Turn on the OMNI.

5. Perform the patient leakage current test as recommended by the analyzer operating
instructions.
Note: Patient leakage current is measured under various conditions of the AC mains and
protective earth conductor. For each condition, the measured leakage current must not
exceed that indicated in Table 3-3.
6. Repeat the patient leakage current test for the SPO2 and temperature patient
connections, using the appropriate test cables.
Note: This test requires a test cable for each patient connector. For example, the ECG test
cable consists of the ECG wires connector, with all conductors shorted together, and
connected to a test lead from the electrical safety analyzer. Test cables for SPO2 and
temperature can be configured in a similar manner, by wrapping each sensor end
individually with aluminum foil filled with conductive gel (only enough gel to ensure
conductivity).
Attach a wire to the foil that is connected to a test lead from the electrical safety analyzer.
Table 3-4: Patient Leakage Current Values
Current (microamps)
N.C. 100(SPO2)，10（ECG, temperature）
S.F.C. 100(SPO2)，50（ECG, temperature）
3.4.2.4 Patient Leakage Current - (Mains Voltage on the Applied Part)

This test measures patient leakage current in accordance with IEC 601-1, clause 19, for
Class I, type CF equipment. In this test, 110% of mains voltage is applied between each
patient connection and earth (power ground). Patient leakage current is then measured
from any individual patient connection to earth.
Note: This test requires the same test cables for each patient connector as described in
paragraph 3.4.2.3.
Warning: AC mains voltage will be present on the applied part terminals during
this test. Exercise caution to avoid electrical shock hazard.
1. Configure electrical safety analyzer as recommended by analyzer operating instructions.

2. Connect monitor’s AC mains power cord to analyzer as recommended by analyzer
3. Connect ECG test cable between ECG connector on OMNI and appropriate input
connector on analyzer.
4. Turn on OMNI.
- 32 -
5. Perform test as recommended by analyzer operating instructions.

Note: Patient leakage current is measured with normal and r everse mains polarity. For
each condition, the measured leakage current must not exceed that indicated in Table 3-4.
6. Repeat test for SpO2 and temperature patient connections, using appropriate test
cables.
Table 3-5: Patient Leakage Current Values— Mains Voltage on Applied Part
Current (microamps)
S.F.C. 5000(SPO2)
50（ECG, temperature）
3.4.2.5 Patient Auxiliary Current

This test measures patient auxiliary current in accordance with IEC 601-1, clause 19, for
Class 1, type CF equipment.
The applied voltage for IEC 601-1 the voltage is 264 volts, 50 to 60 Hz.
Patient auxiliary current is measured between each ECG test lead and b etween each
sensor connection for all possible connections.
Note: This test requires the same test cables for each patient connector as described in
paragraph 3.4.2.3.
1. Configure the electrical safety analyzer as recommended by the electrical analyzer’s
2. Connect the monitor’s AC mains power cord to the electrical analyzer as recommended
by the electrical analyzer’s operating instructions.
3. Connect the patient test lead combination in table 3-6 to the appropriate input connector
on the electrical analyzer.
4. Turn on the OMNI.
5. Perform patient auxiliary current test per table 3-7 as recommended by electrical
analyzer’s operating instructions.
6. Repeat the patient auxiliary current test for each test lead combination as listed in Table
3-5 and measure each patient auxiliary current.
- 33 -
Table 3-6: Test Lead Combinations
First Test Lead Second Test Lead
ECG (LA) ECG (LL)
ECG (LA) ECG (RA)
ECG (LL) ECG (RA)
ECG (LA) Temperature
ECG (LL) Temperature
ECG (RA) Temperature
ECG (LA) SPO2
ECG (LL) SPO2
ECG (RA) SPO2
Temperature SPO2
Table 3-7: Allowable Leakage Current

Current (microamps)
N.C. 100(SPO2)，10（ECG, temperature）
S.F.C. 500(SPO2)，50（ECG, temperature）
- 34 -
SECTION 4: ROUTINE MAINTENANCE
4.1 CLEANING
4.2 PERIODIC SAFETY AND FUNCTIONAL CHECKS
4.3 BATTERIES
4.4 ENVIRONMENTAL PROTECTION
4.1 CLEANING
WARNING: Do not immerse the OMNI or its accessories in liquid or clean with
caustic or abrasive cleaners. Do not spray or pour any liquid on the monitor or its
accessories.
To clean the OMNI, dampen a cloth with a commercial, nonabrasive cleaner and w ipe the
exterior surfaces lightly. Do not allow any liquids to come in contact with the power
connector or switches. Do not allow any liquids to penetrate connectors or openings in the
instrument. For cables, sensors and cuffs, follow the cleaning instructions in the directions
for use that accompany these accessories.
For the touch panel:

(1) Clean and soft clothes with neutral detergent and with isopropyl alcohol may be used for
cleaning.
(2) Do not use any chemical solvent, acidic or alkali solution.
(3) The panel is designed with air groove. Insulation and cushioning pads should be
designed around the edges of the panel to prevent water and dust.
4.2 PERIODIC SAFETY AND FUNCTIONAL CHECKS
The OMNI requires no r outine service or calibration other than cleaning and b attery
maintenance. The following performance verification tests may be used following repair or
during routine maintenance (if required by your local institution).
1. Inspect the exterior of the OMNI for damage.
2. Inspect labels for legibility. If the labels are not legible, contact Infinium Medical Technical
Services Department or your local Infinium Medical representative.
3. Verify that the unit performs properly as described in paragraph 3.3.
4. Perform the electrical safety tests detailed in paragraph 3.4. If the unit fails these electrical
safety tests, do not attempt to repair. Contact Infinium Medical Technical Services
Department or your local Infinium Medical representative.
4.3 BATTERY
If the OMNI has not been used for a long period of time, the battery will need charging. To
charge the battery, connect the OMNI to an AC outlet.
- 35 -
Note: Storing the OMNI for a l ong period without charging the battery may degrade the
battery capacity. A complete battery recharge requires 4 hours. The battery may require a
full charge/discharge cycle to restore normal capacity.
Infinium Medical recommends that the OMNI’s sealed, lead-acid batteries be replaced at
2-year intervals. Refer to Section 5, Disassembly Guide.
4.4 ENVIRONMENTAL PROTECTION
Follow local governing ordinances and recycling plans regarding disposal or recycling
batteries and other device components.
- 36 -
SECTION 5: DISASSEMBLY GUIDE
5.1 INTRODUCTION
5.2 HOW TO USE THIS SECTION
5.3 DISASSEMBLY FLOW CHARTS
5.4 CLOSED CASE DISASSEMBLY PROCEDURES
5.5 FRONT CASE DISASSEMBLY PROCEDURES
5.6 REAR CASE DISASSEMBLY PROCEDURES
5.1 INTRODUCTION
Before disassembling the unit, perform the following:

• Turn off the unit and remove the line cord
• Remove all cables and hoses
• Remove the battery
• Perform all maintenance on a properly grounded work station.
The OMNI can be disassembled down to all major component parts, including:
 PCBs
 Battery
 Cables
 Recorder
 Speaker
 TFT and touch screen
 Function switches and sockets
 Chassis enclosures
The following tools are required:
• Small, Phillips-head screwdriver
• Medium, Phillips-head screwdriver
WARNING: The TFT backlight driver generates high voltage. Exercise

caution when operating monitor with covers open.
WARNING: In order to prevent fingerprints or stain on the products, and get

a cut by sharp edges of glass, clean finger sacks or glove and mask are
required during handing.
Do not touch the viewing area of the touch panel.
Do not handle the tail (connector) of touch panel directly, when you handle
the touch panel. It will cause the problem of combination and reliability.
- 37 -
The step-by-step procedures that are used to access replaceable parts of the OMNI are
illustrated in the Disassembly Sequence Flow Charts. As indicated in the flow charts, the
monitor consists of two main assemblies, the Front Case Assembly and Rear Case
Assembly. The Mainboard assembly is separable from the front case assembly.
The rectangular boxes on the flow charts represent the various spare components or
subassemblies. The Disassembly Flow Charts are organized so that minimum
disassembly is required to remove and replace defective items.
5.3 DISASSEMBLY FLOW CHARTS
FIGURE 5-1: OMNI DISASSEMBLY SEQUENCE FLOW CHART, SHEET 1
- 38 -
FIGURE 5-2: OMNI DISASSEMBLY SEQUENCE FLOW CHART, SHEET 2
- 39 -
Handling Precautions:
a) Since front polarizer is easily damaged, pay attention not to scratch it.
b) Be sure to turn off power supply when inserting or disconnecting from input
connector.
c) Wipe off water drop immediately. Long contact with water may cause discoloration or
spots.
d) When the panel surface is soiled, wipe it with absorbent cotton or other soft cloth.
e) Since the panel is made of glass, it may break or crack if dropped or bumped on hard
surface.
f) Since CMOS LSI is used in this module, take care of static electricity and insure
human earth when
g) Handling.
h) Do not open nor modify the Module Assembly.
i) Do not press or pat the panel surface by fingers, hand or tooling.
j) Do not press the reflector sheet at the back of the module to any directions.
k) In case if a module has to be put back into the packing container slot after once it was
taken out from the
l) Container, do not press the center of the CCFL reflector edge. Instead, press at the
far ends of the CCFL
m) Reflector edge softly. Otherwise the TFT module may be damaged.
n) At the insertion or removal of the Signal Interface Connector, be sure not to rotate nor
tilt the Interface
o) Connector of the TFT module.
p) After installation of the TFT module into an enclosure (Desktop monitor Bezel, for
example), do not twist
q) Nor bend the TFT Module even momentary. At designing the enclosure, it should be
taken into
r) Consideration that no b ending/twisting forces are applied to the TFT module from
outside. Otherwise the
s) TFT module may be damaged.
t) Excessive force or strain to the panel or tail is prohibited for the touch panel.
u) Retain at least 0.3 mm clearance between touch panel and display module.
v) Gasket or cushion pads around the edge of the touch panel may segregate water
and/or dust contamination.
- 40 -
SECTION 6: PARTS
6.1 INTRODUCTION
This section contains exploded views of the Duo monitor, internal modules, and parts list,
along with part numbers, are shown in Table 6-1 partly. “Item No.” corresponds to the
circled callout numbers in Figure 6-1.
Figure 6-1: OMNI Exploded View
- 41 -
Table 6-1: OMNI parts list
Item No. Description Part No.
01 Alarm Indicator-lamp Cover PA-OMN-105
02 Front Case Assembly PA-OMNI-103
03 Silicon Standby Button PA-OMNI-104
04 Touchscreen PA-OMNI-602
05 Keyboard PA-OMNI-331
06 Fix Board for TFT Screen PA-OMNI-004
Mainboard PA-OMNI-309
07 Fix Chassis for Modules PA-OMNI-008
AC/DC Module PA-OMNI-301
DC/DC Module PA-OMNI-302
NIBP Module PA-303
08 Thermal Recorder PA-OMNI-801
09 Recorder Cover PA-OMNI-111
10 Rear Case PA-OMNI-108
11 ETCO2 Module PA-OMNI-334
12 ETCO2 Socket PA-507
13 ETCO2 Cover PA-OMNI-114
14 Shield for Side Panel PA-OMNI-028
15 Side Panel Bracket PA-OMNI-023
16 Speaker PA-OMNI-814
17 Fan PA-OMNI-813
- 42 -
Table 6-2: OMNI Accessories
Description Part No.

NBP Cuff for Adult PA-401
NBP Cuff for Children PA-402
NBP Cuff for Pediatric PA-403
NBP Cuff for Neonate PA-404
SpO2 Sensor for Adult (Analog) PA-405
SpO2 Sensor for Children (Analog) PA-406
SpO2 Sensor for Neonate (Analog,Y type) PA-407
SpO2 Sensor for Adult (Digital) PA-408
SpO2 Sensor for Children (Digital) PA-409
SpO2 Sensor for Neonate (Digital, Y type) PA-410
ECG Cable & Leadwires PA-411
Dual IBP Sensor PA-414
Dual IBP Cable PA-415
Temp Probe for Esophageal/Rectal PA-412
Temp Probe for Skin Surface PA-413
NBP Tubing and Connector PA-417
SpO2 Extension Cable ( 2.1m, DB9 connector) PA-418
Disposable SPO2 Probe for Adult PA-419
Disposable SPO2 Probe for Pediatric PA-420
Disposable SPO2 Probe for Neonate PA-421
Thermal Recorder PA -801
Thermal Paper PA- 802
Battery PA-OMNI-804
ETCO2 Bracket PA -806
Holder PA-OMNI-807
AC Power Cord PA -810
Grounding Clip & Line PA -812
- 43 -
SECTION 7: TROUBLESHOOTING
7.1 INTRODUCTION
7.3 WHO SHOULD PERFORM REPAIRS
7.4 REPLACEMENT LEVEL SUPPORTED
7.5 OBTAINING REPLACEMENT PARTS
7.6 TROUBLESHOOTING GUIDE
7.1 INTRODUCTION
This section explains how to troubleshoot the OMNI if problems arise. Tables are supplied
that list possible monitor difficulties, along with probable causes, and recommended
actions to correct the difficulty.
Use this section in conjunction with Section 4, Performance Verification. And Section 5,
Spare Parts. To remove and replace a part you suspect is detected, follow the instructions
in Section 6, Disassembly Guide. The circuit analysis section in the Technical Supplement
offers information on how the monitor functions.
7.3 WHO SHOULD PERFORM REPAIRS
Only qualified service personnel should open the monitor housing, remove and replace
components, or make adjustments. If your medical facility does not have qualified service
personnel, contact Infinium Medical Technical Services or your local Infinium Medical
representative.
7.4 REPLACEMENT LEVEL SUPPORTED
The replacement level supported for this product is to the printed circuit board (PCB) and
major subassembly or component level. Once you isolate a suspected PCB, follow the
procedures in Section 4, Disassembly Guide, to replace the PCB with a known good PCB.
Check to see if the trouble symptom disappears and that the monitor passes all
performance tests. If the trouble symptom persists, swap back the replacement PCB with
the suspected malfunctioning PCB (the original PCB that was installed in the monitor
before you started troubleshooting) and c ontinue troubleshooting as directed in this
section.
7.5 OBTAINING REPLACEMENT PARTS
Infinium Medical Technical Services provides technical assistance information and
- 44 -
replacement parts. To obtain replacement parts, contact Infinium Medical or your Infinium
Medical representative.
7.6 TROUBLESHOOTING GUIDE
Problems with the OMNI are separated into the categories indicated in Table 7-1. Refer to
the paragraph indicated for further troubleshooting instructions.
NOTE: Taking the recommended actions discussed in this section will correct the majority
of problems you may encounter. However, problems not covered here can be resolved by
calling Infinium Medical Technical Services or your local representative.
Table 7-1: Problem Categories

Problem Area Refer to
Paragraph
1. Power
• No power-up
7.6.1
• Fails power-on self-test
• Powers down without apparent cause
2. Switches
7.6.2
• Monitor does not respond properly to switches
3. Display/Audible Tones
• Display does not respond properly 7.6.3
• Tones do not sound properly
4. Operational Performance
• Displays appear to be operational, but monitor shows no readings
• Modules trouble 7.6.4
• Suspect readings
• Recorder not responding
5. Serviceable Hardware Error Messages 7.6.5
- 45 -
7.6.1 Power
Table 7-2 Lists recommended actions to address power problems

Condition Recommended Action
1. The OMNI fails to power-up 1. Ensure power cord is plugged into operational AC
when the On/Standby switch is outlet of appropriate voltage and frequency. Ensure
pressed. green AC SOURCE indicator is lit. If indicator is not
lit, repair power supply assembly.
2. Check fuses located on EMI filter above AC inlet
receptacle. Replace fuses if necessary.
3. Inside monitor, check main cables and ensure
that it is connected to PCBs and power supply
assembly.
4. Ensure keyboard is connected with power supply
PCB. If connection is good, repair keyboard.
5. If the problem persists, replace power supply
PCB.
2. The OMNI turns on, then shuts 1. Ensure AC power cord is connected and green
off and no error code is displayed. AC SOURCE indicator is lit, or ensure green
BATTERY CHARGING indicator is lit.
If the monitor operates successfully, the battery may
be discharged.
2. Recharge battery as directed in paragraph 3.3.1.
If battery fails to hold charge, replace battery or
battery housing.
3. If problem persists, check power supply PCB.
4. If problem persists, check mainboard.
7.6.2 Switches
Table 7-3 lists recommended actions to address problems with the On/Standby switch
and touch screen panel.
- 46 -
Table 7-3: Switches/Knob Problems
1. OMNI fails to power-up when 1. Take steps as noted in paragraph 7.6.1.
the On/Standby switch is pressed. 2. If the problem persists, check whether there is a
trouble on the power supply PCB.
2. OMNI powers up, but some or 1. Ensure keyboard connector and touch screen
no any respond on the touch panel are plugged into mainboard. If connection is
screen panel. good, check the keyboard or the touch screen
panel.
7.6.3 Display/Audible Tones
Table 7-4 lists recommended actions to address problems with the display and audible
tones.
Table 7-4: Display/Audible Tones Problems
1. TFT screen is not illuminated or 1. Ensure status indicator LED, located on the
no display. mainboard is flashed. Otherwise replace the FPGA
(UF1) microprocessor chip or mainboard.
2. Ensure TFT cable is connected to mainboard.
4. If problem persists, check TFT assembly.
2. OMNI responds to click touch, 1. Ensure speaker cable is connected to power
but click tone fails to sound. supply assembly and keyboard.
2. If problem persists, check speaker assembly.
3. If problem persists, check power supply PCB or
touch panel.
3. Audible alarm does not sound. 1. Verify alarm volume setting in Alarm/Limits menu.
2. Ensure speaker cable is connected to power
supply assembly.
3. If problem persists, replace speaker assembly.
- 47 -
7.6.3 Operational Performance
Table 7-5 lists recommended actions to address problems related to operational

performance.
Table 7-5: Operational Performance Problems
1. Monitor appears to be 1. Ensure internal ECG, temperature and SPO2
operational, but physiological cables are connected to mainboard. Ensure hoses
values are suspect or nonexistent. in pneumatic system are properly connected, and
NIBP pump motor is connected to power supply
PCB.
3. If problem persists, check TFT screen.
2. ECG measurement has 1. Check the “HR CALCULATE SOURCE” item’s
waveforms display, but no heart lead selection in the “ECG setup” menu.
rate value displays. 2. Check whether the QRS waveform is smooth and
evident.
3. NIBP module can’t be inflated 1. Check whether the pump is bad.
2. Check the NIBP module’s power supply.
4. Inflation pressure can’t reach 1. The maximum inflation pressure value cannot
the normal level. exceed 150mmHg (20kPa).
2. Check whether the pump is bad.
3. Check whether there has an air leakage trouble.
If it exists, check whether the valves, cuff and
relevant connectors work normally.
5. Air leak Air leakage in NIBP cuff or hose, check all
connections and test the cuff tightness using venous
stasis.
6. NIBP Signal weak NIBP weak or unstable oscillation signal due to:
1. Improper cuff position or attachment, small air
leakage.
2. Weak or abnormal blood circulation.
3. Slow heart rate associated with artifacts.
4. Patient is moving or disturbed during
measurement.
7. Recorder paper will not 1. Open recorder door and check paper is present.
advance. Press recorder module firmly into monitor to ensure
recorder module is fully engaged with connector on
mainboard.
- 48 -
2. Cycle power on m onitor. Recorder should

execute a line feed at conclusion of power up
sequence.
3. If problem persists, ensure main ribbon cable is
connected to recorder PCB, power supply, and
mainboard.
4. If problem persists, check recorder.
5. If problem persists, check recorder PCB.
8. Recorder paper will advance, 1. Open recorder door and check paper is oriented
but paper remains blank when correctly; paper should exit from bottom of roll. See
recording should be present. user’s manual for an illustration of correct paper
orientation.
2. If problem persists, replace recorder module.
7.6.5 Serviceable Hardware Error Messages

The error messages that correspond to hardware problems, and the recommended
actions to take should such an error encountered.
Table 7-6: Serviceable Hardware Error Messages
Messages Recommended
ECG Com Error ECG communication trouble
1. Ensure ECG module is properly connected with relevant periphery
modules.
2. Check the power supply to the ECG PCB.
3. Check ECG module section.
4. If problem persists, replace ARM-FGPA PCB.
ECG Lead Off 1. The relevant wire is disconnected or off the patient.
ECG Lead RA Off
2. If lead I is lead off, check whether lead RA and lead LA are
ECG Lead LA Off
ECG Lead RA LA Off attached well.
ECG Lead LL Off
3. If all leads are lead off, check the lead RL is attached well. Or
ECG Lead RA LL Off
ECG Lead LA LL Off replace the mainboard.
ECG Lead RA LA LL Off
ECG Lead V Off
ECG Lead RA V Off
ECG Lead LA V Off
ECG Lead RA LA V Off
ECG Lead LL V Off
ECG Lead RA LL V Off
ECG Lead LA LL V Off
SpO2 Com Error SPO2 communication trouble
1. Ensure SPO2 module is properly connected with mainboard.
- 49 -
2. Check the power supply to the SPO2 PCB.

3. Replace SPO2 circuit.
4. If problem persists, replace mainboard.
Searching For Pulse. . . Monitor is searching for pulse oximetry signal.
Search Too Long Monitor searches the pulse oximetry signal for a long time.
1. Check whether the SPO2 sensor’s LED is lit, when the sensor is
clipped a finger, this LED should lit normally. Otherwise it is
flashed.
2. Reapply the SPO2 sensor.
3. Replace the SPO2 transducer.
Cuff Error Ensure the cuff’s type is correct.
Reset error！ 1. Replace NIBP module.
Zero reset error！ 1. Replace NIBP module.
Serial error 1. Replace NIBP module.
NIBP selfcheck error！ Replace NIBP module.
NIBP inter error！ Replace NIBP module.
Patient type error！ Ensure the cuff’s type is correct.
Temp1 Probe Off The temperature 1 probe is disconnected or off the patient.
Temp2 Probe Off The temperature 2 probe is disconnected or off the patient.
Resp Com Error The respiration 1 probe is disconnected or off the patient.
IBP1 Sensor Off The IBP1 transducer is disconnected or off the patient.
IBP2 Sensor Off The IBP2 transducer is disconnected or off the patient.
EtCO2 Sensor Off The ETCO2 transducer is disconnected or off the patient.
GAS Sensor Off The gas sensor is disconnected or off the patient.
Multi-Gas Module Error 1. Ensure multi-gas module is properly connected with mainboard.
2. Check the power supply to the multi-gas.
3. Replace multi-gas circuit.
ERAM Error! err_bits = Fault ERAM circuit on the main board. Contact authorized service
0xFFFF
personnel.
Low Battery The battery’s capacity is low
Recorder UnLink！ 1. Printer is not connected or is not turned on.
2. Printer cable is loose or broken.
Recorder No Paper There is no paper in recorder
- 50 -
SECTION 8: PACKING FOR SHIPMENT

8.1 GENERAL INSTRUCTIONS
8.2 REPACKING IN ORIGINAL CARTON
8.3 REPACKING IN A DIFFERENT CARTON
8.1 GENERAL INSTRUCTIONS
Pack the monitor carefully. Failure to follow the instructions in this section may result in
loss or damage to the monitor. If the original shipping carton is not available, use another
suitable carton.
Prior to shipping the monitor, contact Infinium Medical’s Technical Services Department or
your local Infinium Medical representative. Mark the shipping carton and any shipping
documents. Return the monitor by any shipping method that provides proof of delivery. To
pack the monitor for return, disconnect all cables. It is not necessary to return sensors,
patient cables, NIBP hose and cuff, temperature probe, or external power supply.
8.2 REPACKING IN ORIGINAL CARTON
If available, use the original carton and packing materials. Pack the monitor as follows:
1. Place the monitor in original packaging.
2. Place in shipping carton and seal carton with packaging tape.
3. Label carton with shipping address, return address and RGA number, if applicable.
8.3 REPACKING IN A DIFFERENT CARTON
If the original carton is not available, use the following procedure to pack the
Monitor:
1. Place the monitor in a plastic bag.
2. Locate a corrugated cardboard shipping carton with at least 200 pounds per square
inch (psi) bursting strength.
3. Fill the bottom of the carton with at least 2 inches of packing material.
4. Place the bagged unit on the layer of packing material and fill the box completely
with packing material.
5. Seal the carton with packing tape.
6. Label the carton with the shipping address, return address.
- 51 -
SECTION 9: SPECIFICATIONS
SAFETY
Meet the requirement of EN60601 series, CE marking according to MDD93/42/EEC
Equipment not suitable for use in the presence of a flammable anaesthetic mixture with air or with
oxygen or nitrous oxide
Type of Protection: Class I (on AC power) , Internally powered (on battery power)
Degree of Protection: Type BF, defibrillation-proof CF - Applied part
Sterilization or Disinfection 70% isopropyl alcohol solution or a nonstaining disinfectant.
methods:
Operation Mode: Continuous Operation
Protection Against Ingress IPX0
of Liquid’s:
APPLICATION
Neonatal, pediatric and adult patients
Physical Dimensions & Weight
Base Unit: 310×270×145mm
Weight: 4.7kgs
PEFORMANCE SPECIFICATIONS
Display: 10.1〞color TFT
Resolution: 1024×860
Trace: 3 or 6 waveforms
Waveforms ECG(I, II, III, aVR, aVL, aVF, V1-V6), PLETH, RESP, IBP1, IBP2,
ETCO2
Indicator: Alarm indicator
Power indicator
QRS beep and alarm sound
Trend time: From 30 minutes to 72 hours
ECG
Input: 5 lead or 3 lead ECG cable and s tandard AAMI line for
connection
Lead Choice: I，II，III，aVR，aVF，aVL，V
Gain Choice: ×0.5，×1.0，×2.0
CMRR (common mode >100 dB at 50 Hz or 60 Hz
rejection ratio):
Frequency Characteristic: 0.67～40 Hz （+3dB attenuation）
ECG Waveforms: 7 channels
Sweep Speed: 12.5, 25 and 50 mm/s
HR Display Range: 30～300bpm
Accuracy: ±1bpm or ±1%, whichever is greater
Alarm Limit Range Upper limit:80～400bpm
Lower limit: 20～150bpm
Input Dynamic Range: ±5 mV AC
Defibrillator Discharge: <5 sec
Differential Input mpedance: >5 MΩ
Bandwidth: 0.5 to 30 Hz (filter mode), 0.5 to 40 Hz (non filter mode)
Electrode Offset Potential ±300 mV

Tolerance:
Input Signal Range: ±5 mV
Recovery: <8 sec
Standards:
Meets the performance standards of ANSI/AAMI EC13:2002. Instead of a 1 mV
standardization voltage (section 4.2.2.9), a fixed, 1 cm reference bar is always present in the ECG
display, along with the ECG size setting expressed in mV/cm. The following references particular
sections of ANSI/AAMI EC13:2002.
- 52 -
Respiration, leads-off Sinusoidal signal, 260 μA, 40.5 kHz

sensing waveform. Noise Suppression: RL drive gain 44 dB max., max. voltage 1.8
Noise suppression Vrms
4.1.2.1(b)
Tall T-wave rejection. Exceeds ANSI/AAMI EC 13 Sect. 4.1.2.1(c) , Recommended less
4.1.2.1(c) than 1.2 mV T-Wave amplitude
Heart Rate Averaging Normally, heart rate is computed by averaging the 12 most recent
Method RR intervals. For runs of PVCs, up to 8 RR intervals are
4.1.2.1(d) averaged to compute the HR. If each of 4 consecutive RR
intervals is greater than 1200 ms (that is, rate less than 50 bpm),
then the 4 most recent RR intervals are averaged to compute the
HR. Thereafter computing by increasing 1 RR interval till recover
12 RR intervals.
The fresh rate for displaying HR value is 1 second.
Response to a) Ventricular bigeminy - 80 BPM
irregularrhythm. 4.1.2.1(e) b) Slow alternating ventricular bigeminy - 60 BPM.
c) Rapid alternating ventricular bigeminy - 120 BPM
d) Bi-directional systoles - 90 BPM
Heart rate meter response HR change from 80 to 120 bpm:
time. 4.1.2.1(f) Average: 10 seconds
HR change from 80 to 40 bpm:
Average: 10 seconds
Heart rate meter response 0.5 mV Average Time to Alarm
time. 4.1.2.1(g) 1 mV 10 sec
2 mV 10 sec
Waveform 4(b),Amplitude 10 sec
1 mV Average Time to Alarm
2 mV 10 sec
4 mV 10 sec
Pacemaker pulse rejection. With the exceptions noted below, the monitor will reject all
4.1.4.1, 4.1.4.3 pacemaker pulses having amplitudes of ±2 to ±700 mV and
pulse widths from 0.1 to 2.0 ms.
RESPIRATION
Measure Method: RA-LL impedance
Range: 0～120 rpm
Accuracy + 3 rpm
Alarm Upper-lower Limit Upper limit: 6～120 rpm，
Lower limit: 3～120 rpm
Sweep Speed: 12.5 and 25mm/s
NIBP
Measuring Technology: Automatic oscillating measurement
Cuff Inflating: <30s（0～300 mmHg，standard adult cuff）
Measuring Period: AVE<40s
Mode Manual, Auto, STAT
Measuring Interval in AUTO 2 min～4 hrs
Mode
Pulse Rate Range: 30 bpm～250 bpm
Measuring Range: Adult/Pediatric Mode
SYS 40～250 (mmHg)
DIA 15～200 (mmHg)
Neonatal Mode
SYS 40～135 (mmHg)
DIA 15～100 (mmHg)
Resolution: 1mmHg
Pressure Accuracy: Maximum Mean error: ±5mmHg
Maximum Standard deviation: 8mmHg
- 53 -
Overpressure Protection: Adult Mode 280(mmHg)

Neonatal Mode 150 (mmHg)
Alarm Limit: SYS 5 0～240 mmHg
DIA 1 5～180 mmHg
TEMPERATURE
Range: 25～50（℃）
Accuracy: + 0.2℃（25.0～34.9℃）
+ 0.1℃（35.0～39.9℃）
+ 0.2℃（40.0～44.9℃）
+ 0.3℃（45.0～50.0℃）
Display Resolution: 0.1℃
Alarm Upper-lower Limit: Upper limit 0～50℃，
Lower limit 0～50℃
Channel: 2 channels
Alarm Limit: 10～50（℃）
SPO2
ASpO 2 : Anti-motion SpO 2
SpO 2 % Range: 0～100%
SpO 2 Accuracy: + 2%（70～100%,non-motion）
+ 3%（70～100%, motion）
Pulse Rate Range: 30-250 bpm
Pulse Rate Accuracy: ±2 bpm(non-motion)

±3 bpm (motion)
Alarm Upper-lower Limit: Upper limit 70～100%，
Lower limit 70～100%
SpO 2 Probe: Red light LED wavelength 660nm±5nm
Infrared light LED wavelength 940nm±10nm
IBP(OPTION)
Measurement Range: -10～300mmHg
Channel: 2 channels
Pressure transducer: Sensitivity, 5µV/V/mmHg
Impedance range: 300～3000Ω
Transducer sites: ART, PA,CVP, RAP, LAP, ICP
Resolution: 1mmHg
Accuracy: ±1mmHg or ±2%, whichever is greater
Alarm range: -10～300mmHg
EtCO 2 (OPTION)
Mode of Sampling: Sidestream or Mainstream
Principle of Operation: Non-dispersive infrared (NDIR) single beam optics, dual
wavelength, no moving parts.
CO 2 measurement Range: 0 to 150 mmHg (0 to 19.7%, 0 to 20 kPa)
CO 2 Calculation Method: BTPS (Body Temperature Pressure Saturated)
CO 2 Resolution: 0.1mmHg(0-69mmHg), 0.25mmHg(70-150mmHg)
CO 2 Accuracy: 0～40 mmHg ± 2 mmHg
41～70 mmHg ± 5% of reading
Above 80 breath per minute ± 12% of reading
Sampling rate: 100Hz
Respiration Rate: 2～150 bpm
Respiration Rate accuracy: ±1 breath
Response Time: <3 seconds - includes transport time and rise time
- 54 -
Inspired CO 2 measurement 3～50 mmHg

Range:
NETWORKING
Wired Networking Industry standard: IEEE 802.3 wired network
Connected bedside number: Up to 16 bedside monitors
RJ45 interface or RS232 serial port
Wireless Networking Up to 100m indoors
Frequency Range: 2.412～2.484 GHz
Industry standard 802.11b/g wireless
Supports TCP/IP and UDP/IP Protocols
POWER
Source: External AC power and internal battery
AC Power: 100～240VAC, 50/60Hz, 150VA
Battery: Rechargeable Sealed Lead
Type: FB 1223 12v-2.3Ah
Operating time under the normal condition: 1 hour
Operating time after the first alarm of low battery: 10 Minutes
Manufacturer: Pilot Battery Co.,Ltd.
Charge Time: 4 hours
Operating Time: 1 hour
Fuse: T 3.0A/250V
ENVIRONMENTAL SPECIFICATIONS
Temperature: Operating: 5～40 °C
Storage: -10～45 °C
Humidity Range: Operating: ≤80 %
Storage: ≤80 %
RECORDER (OPTION)
Record Width: 48 (mm)
Paper Speed: 25 (mm/s)
Trace: 2 or 3
- 55 -

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SERVICE MANUAL

SECTION 2: INTRODUCTION AND SYSTEM DESCRIPTION .......................................................... 6

2.2.1.1 PIN ASSIGNMENT AND DESCRIPTION FOR AC-DC MODULE .......................................... 8

2.2.1.2 PIN ASSIGNMENT AND DESCRIPTION FOR DC-DC MODULE .......................................... 9

2.2.1.3 DC-DC MODULE TEST POINTS..................................................................................... 11

2.2.2 MAINBOARD (ARM-FPGA SYSTEM，ERT MODULE（ECG, RESP, TEMP,SPO2）) .......... 11

2.2.2.1 PIN ASSIGNMENT AND DESCRIPTION FOR MAINBOARD .............................................. 12

2.2.2.2 MAINBOARD TEST POINTS........................................................................................... 14

2.2.2.3 FPGA ................................................................................................................................ 14

2.2.2.4 ARM (ADVANCED RISC MACHINE).................................................................................. 14

2.2.2.5 ERT MODULE（ECG, RESP, TEMP, SPO2） ................................................................... 15

2.2.3 NIBP MODULE ................................................................................................................. 16

2.2.3.1 PIN ASSIGNMENT AND DESCRIPTION FOR NIBP MODULE ............................... 19

2.2.4 SPO2 MODULE................................................................................................................ 19

2.2.5 DISPLAY ........................................................................................................................... 20

2.2.5.1 PIN ASSIGNMENT FOR TFT LCD PANEL DRIVING ............................................... 20

2.2.6 KEYBOARD (SWITCHES) .............................................................................................. 22

2.2.7 TOUCH PANEL ................................................................................................................ 22

2.2.8 SPEAKER ......................................................................................................................... 23

2.2.9 RECORDER ..................................................................................................................... 23

2.2.9.1 PIN ASSIGNMENT FOR RECORDER MODULE ...................................................... 25

2.2.10 RS-232 ............................................................................................................................ 26

SECTION 3: PERFORMANCE VERIFICATION................................................................................. 27

3.3.2 BATTERY PERFORMANCE TEST ................................................................................ 28

3.3.3 POWER-ON SELF-TEST ................................................................................................ 28

3.3.4 HARDWARE AND SOFTWARE TESTS ........................................................................ 29

3.3.5 OPERATION WITH A HUMAN SUBJECT ..................................................................... 30

3.4 SAFETY TESTS............................................................................................................................. 30

SECTION 4: ROUTINE MAINTENANCE ............................................................................................ 35

SECTION 5: DISASSEMBLY GUIDE.................................................................................................. 37

SECTION 6: PARTS ............................................................................................................................. 41

SECTION 8: PACKING FOR SHIPMENT ........................................................................................... 51

SECTION 9: SPECIFICATIONS .......................................................................................................... 52

1.1 MANUAL OVERVIEW

1.2 WARNINGS, CAUTIONS AND NOTES

1.3 OMNI PATIENT MONITOR DESCRIPTION

1.4 RELATED DOCUMENTS

To perform test and troubleshooting procedures and to understand the principles of

2.1 SYSTEM OVERVIEW

2.1.1 The Complete OMNI Patient Monitor System

The monitor is essentially a b attery-powered instrument. An internal charging unit is

2.2 SYSTEM BLOCK DIAGRAM

FIGURE 2-1: OMNI SYSTEM BLOCK DIAGRAM

2.2.1 POWER SYSTEM

FIGURE 2-2: POWER SYSTEM BLOCK DIAGRAM

2.2.1.1 PIN ASSIGNMENT AND DESCRIPTION FOR AC-DC MODULE

FIGURE 2-3: PIN ASSIGNMENT FOR AC-DC MODULE

2.2.1.2 PIN ASSIGNMENT AND DESCRIPTION FOR DC-DC MODULE

FIGURE 2-4: PIN ASSIGNMENT FOR DC-DC MODULE

ASPO2:（Communicate with SPO2 module）

NET：(To RS232 Interface)

CONTROL:（Communicate with mainboard）

4 DVCC , +5vdc for mainboard power supply

NBP：（To NIBP module）

PRINTPOW：（To recorder module）

DC：（To AC/DC module）

FLY2：(To fan connector)

2.2.1.3 DC-DC MODULE TEST POINTS

2.2.2 MAINBOARD (ARM-FPGA SYSTEM，ERT MODULE（ECG, RESP, TEMP,SPO2）)

The ARM microcontroller completes functions of management of modules,

Serial User Indicator

FIGURE 2-5: MAINBOARD BLOCK DIAGRAM

2.2.2.1 PIN ASSIGNMENT AND DESCRIPTION FOR MAINBOARD