G30-G40 Servicio ENG

G30/G40
Patient Monitors
Service Guide
English
G30/G40
Patient Monitors
Service Guide
English
Product Information
Product model: G30/G40
Product name: Patient Monitor
Manufacturer
Shenzhen Goldway Industrial Inc.
Registered/Production Address:
No. 2 Tiangong Road, Nanshan District, Shenzhen, P. R. China 518057
Tel: +86 755 26980999

Fax: +86 755 26980222
Edition
Third Edition: Decemeber 2012
Shenzhen Goldway Industrial Inc.

All Rights Reserved.
Regulatory and Safety Specifications
Standard
The products are made under the ISO9001 and ISO13485 quality system certified by TUVPS. The products
have passed CE certification.
Declaration
The G30 and G40 monitors are Class IIb devices and comply with the requirements of the Council Directive
93/42/EEC concerning medical devices and carry CE-marking accordingly.
Authorized EU Representative
Shanghai International Holding Corp.GmbH (Europe)
Eiffestrasse 80, 20537
Hamburg, Germany
Tel: 0049-40-2513175
Fax: 0049-40-255726
Rx Only
Caution: United States Federal Law restricts the devices to sale by or on the order of a physician.
2 G30/40 Patient Monitors Service Guide

Explanation of Symbols
The following symbols appear on the monitor and its packaging.
Table 1 Monitor and Packaging Symbols
Symbol Description Symbol Description
CE mark Fragile, handle with care
Recyclable Keep upright
Recovery Maximum stacking
Humidity limitation Caution, consult accompanying

documents
BF applied part: including F CF applied part: including F

applied part (float/insulation) applied part (float/insulation)
and defibrillation-proof and defibrillation-proof
function. function.
Temperature limitation Atmospheric limitation
Keep dry Param Menu key
On/Standby key Waveform Freeze key
Main Menu key Alarm silence key
Print key NIBP key
SpO2 probe connector C.O. connector
ECG connector CO2 connector
G30/40 Patient Monitors Service Guide 3

Table 1 Monitor and Packaging Symbols(Continued)
Symbol Description Symbol Description
IBP1 connector IBP2 connector
NIBP cuff connector TEMP1 connector
TEMP2 connector Gas input
AC Power LED Charging LED
Date of manufacture Manufacturer address
Equipotential grounding post Dangerous voltage
EU representatives Display output
Nurse call connector ECG analog output port
Consult Instructions for use Serial Number
Protective grade USB port
Gas output Fuse
Protective grounding Ethernet port

Safety Standards
The following table describes the safety standard of the G30/G40 patient monitors.
Table 2 Safety Standards
Parameter Specification
Protection Class Class I, anti-shock, externally and internally powered equipment, per
IEC 60601-1
Degree of Protection Type CF defibrillator-proof: per IEC 60601-1

Degree of noxious-liquid proof as IPX1
Anti-shock degree as combination of BF and CF applied part.
According to the degree of safety of application in the presence of a
flammable anesthetic mixture with air or with oxygen or nitrous
oxide, the equipment is not suitable for use in the presence of a
flammable anaesthetic misture with air or with oxygen or nitrous
oxide.
Sterilization and disinfection As recommended by manufacturer
Mode of Operation Continuous
Product Support and Warranty Information

Goldway warranties the G30/G40 Patient Monitor for one year.
Keep the packing case for transport, storage, or maintenance.
Goldway is responsible for the safety, reliability and performance of the monitor when the:
• product is assembled, upgraded, altered, or maintained by authorized service representatives.

• location where the product is placed is that of a typical hospital environment.
• product is used according to this guide.
Goldway is not responsible for damage to the monitor under the following circumstances:
• damage is caused by the following:

– improper operation.
– improper connection of the monitor to other devices.
– accidental impact.
• the monitor is altered without written authorization from Goldway.
• the serial number of the monitor is removed or becomes illegible.

After Sales Service
When you need product support:
1. Contact your local Goldway representative.
2. For further support, contact Goldway Customer Service Department.
Customer Service Department of Shenzhen Goldway Industrial Inc.

No. 2 Tiangong Road, Nanshan District, Shenzhen, P. R. China 518057
International call center hours:
Monday – Friday (except Chinese statutory holidays)

BJT 08:30 – 12:00, 13:00 – 17:30 (GMT+8)
Tel: +86 755 86278308

Fax: +86 755 86278392
E-mail: goldway.service@philips.com
Service and support are available in Chinese and English only.
Before calling for service, note the following information:
• Model and serial number of the monitor

• Monitor problem
Safety Conventions
The guide uses the following conventions for Notes, Cautions, and Warnings.
Note — A Note calls attention to an important point in the text.
Caution A Caution calls attention to a condition or possible situation that could damage or destroy the product
or the user’s work.
Warning A Warning calls attention to a condition or possible situation that could cause injury to the user and/or
patient.

Safety Requirements
Note — The safety indications in this chapter apply to general monitor use. Safety indications in other
chapters apply to specific monitor measurements.
Follow the instructions of this service guide when using the monitor. However, conventional medical practices
always supersede this document. Significance of safety requirements set forth here in this manual is not in
order of reading sequence.
Warning Never rely exclusively on the alarm system for patient monitoring. Low alarm limits or turning the alarm
off during patient monitoring may result in patient danger. The most reliable method of patient
monitoring combines close, personal surveillance along with the correct operation of the monitor. You
must periodically check that monitor alarms are working properly.
Only use the monitor on one patient at a time.
Never use the monitor to monitor apnea.
Anyone who connects additional equipment to the signal input port or signal output port configures a
medical system and is therefore responsible to ensure that the system complies with the requirements of
standard IEC 60601-1. Never permanently install equipment connected to the signal input or output
ports. If in doubt, contact Goldway.
The monitor is not for home use.
The monitor is not for diagnostic or therapeutic use.
To avoid confusing patient records, clear all historical data of the last patient before monitoring a new
patient.
To avoid personal injury, only use accessories and parts produced or recommended by Goldway.
Ensure that the monitor is in good working condition and is placed in the proper position before
monitoring a new patient.
For pacemaker patients, rate meters may continue to count the pacemaker rate during occurrences of
cardiac arrest or arrhythmia. Do not rely entirely on rate meter alarms. Keep pacemaker patients under
close curveillance. See this manual for disclosure of the pacemaker pulse rejectioncapability of this
instrument.
Never use the monitor during MRIs or CT scans.
Never use cables with exposed conductors. Only use undamaged cables and connectors to avoid personal
injury.
Never simultaneously touch the patient and the input or output terminal of the monitor.
The monitor can be used with electrosurgical devices. To avoid burns or death, ensure that the
electrosurgical circuitry is properly connected.
Ensure that the patient is not connected to any metal, the surface of any conductors, or grounded parts of
any devices when a defibrillator is in use. Never touch the patient, table, or instruments during
defibrillation.
Never use the monitor in an environment of anesthetic gases.
Disconnect the AC power supply and remove the battery before disassembling the monitor.

Caution To avoid personal injury, only use accessories and parts producted or recommended by Goldway. Otherwise,
damage to the monitor can occur.
Position power cords and other cables to prevent tangling, patient contact, or electrical interference.
Always use a three-wire receptacle in order to properly ground the monitor. Use the monitor on battery
power only if you suspect any problem with external grounding or wiring.
The battery will discharge over time when stored inside a monitor with no AC power. Keep the monitor
plugged in when storing it and perform a monthly check of battery power.
If multiple devices are connected to a patient, the sum of the leakage currents may cause a dangerous
situation. Therefore, qualified service representatives should always perform current leakage tests before
setting up the connections. This ensures that leakage is within limits and prevents personal injury and
environmental damage. If any question remains, consult the manufacturer for correct usage.
The monitor must conform with the international standard IEC 60601-2 and other applicable EMC
standards. Interference takes place when electromagnetic energy is extremely high. Ensure that any
nearby instruments are also in compliance with EMC standards. Never turn on or use portable
communication devices like mobile phones or portable dual-channel radios near a monitor.
Unknown electromagnetic interference could be caused by radio transmitters or nearby televisions.

Move patient monitors away from these devices or insert shielding materials around the monitor.
Any devices connected to the monitor must comply with the IEC standard for that device. For example,
data processing devices must comply with IEC 60905 and medical devices must conform to IEC 60601-1.
The whole system must comply with the most recent IEC 60601-1-1 standards.
To ensure monitor safety, all service parts and accessories must comply with IEC 60601 standards. The
system configuration of the monitor must comply with IEC 60601-1-1 medical electrical standards.
If patient data is lost, closely monitor the patient or replace the monitor immediately until the monitor
restores normal function again.
To reduce the hazard of burns in high-frequency surgical neural connections, the leads and connectors must
be located away from the surgical site. Keep cables away from other devices.
Ensure that qualified service representatives annually calibrate and maintain the monitor.
Periodically check all reusable accessories for damage. Replace and dispose of damaged accessories
when necessary according to your local hospital waste disposal regulations.
ECG electrodes are displosable accessories for damage. Always properly dispose of ECG electrodes
according to your local hospital waste disposal regulations.
Clean and sterilize the monitor and accessories according to local requirements. Turn off the monitor
and disconnect the power cords before cleaning or sterilization.
Keep all monitor packing materials away from children, or dispose of them in accordance with your
local environmental regulations.
Always properly dispose of the monitor and all accessories. Dispose of batteries according to your local
regulations. Never incinerate batteries or expose them to high temperatures. Contact Goldway if you
have any questions concerning disposal.
Ensure that no water condenses into or on the monitor. Condensation can occur from changes in
temperature or exposure to humidity.

Table of Contents
1 General Introduction
1.1 Who Should Read This Guide. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-1
1.2 Repair Strategy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-1
1.3 Site Requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-2
1.3.1 Space Requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-2
1.3.2 Environmental Requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-2
1.4 G30/G40 Patient Monitors Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-3
1.4.1 Power Specifications. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-3
1.4.2 Main Components . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-3
1.4.3 Indications for Use . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-4
1.4.4 Intended Use . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-4
1.4.5 Networking Capabilities . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-4
1.4.6 RJ45 Port. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-4
1.4.7 HL7 Format. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-5
1.5 Before You Begin . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-5
1.6 Installing the Monitor . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-5
1.7 Before Powering On . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-6
1.8 Monitor and Accessories Inspection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-6
1.9 Setting Demo Mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-7
1.10 Configuring a Network . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-7
1.11 Upgrading the Software . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-9
2 Maintenance
2.1 Manufacturer’s Responsibility . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-1
2.2 Testing and Inspection Guidelines . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-1
2.3 Recommended Frequency . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-2
2.4 Required Test Equipment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-2
2.5 Test Recording . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-4
2.6 Performance Verification Tests. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-5
2.6.1 Visual Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-5
2.6.2 Power Supply Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-5
2.6.3 Display Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-5
2.6.4 Speaker Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-5
2.6.5 ECG Test. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-6
2.6.6 Respiration Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-6
2.6.7 Temperature Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-6
2.6.8 IBP Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-6
2.6.9 Pulse SpO2 Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-7
2.6.10 C.O.Test (BT and TI, G40 Only) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-7
2.6.11 NIBP Test and Calibration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-8
2.6.11.1 To Test the Overpressure. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-9
2.6.11.2 To Calibrate the NIBP. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-9
2.6.12 Microstream CO2 Calibration. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-9
2.6.13 IBP Calibration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-10
2.6.14 Networking Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-10
2.7 Electrical Safety Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-10
2.7.1 System Enclosure Leakage . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-11
2.7.2 S(2) Protective Earth Continuity. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-12
2.7.3 Patient Leakage Current with Mains Voltage . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-12
G30/40 Patient Monitors Service Guide Contents-1

2.8 Recorder Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-13
3 Theory of Operation
3.1 System Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-1
3.2 Theory of Operation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-1
3.2.1 System Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-1
3.2.2 Block Diagram Components. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-2
3.2.3 ARM Module . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-2
3.2.4 System Module . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-2
3.2.5 I/O Module Assembly. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-3
3.2.6 Speaker . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-3
3.2.7 Recorder . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-3
3.2.8 AC/DC Power Module . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-3
3.2.9 Keys and Navigation Wheel . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-3
3.2.10 NIBP Processing . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-3
3.2.11 SpO2 Processing . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-4
3.2.12 ECG Processing . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-4
3.2.13 IBP Processing . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-4
3.2.14 Temperature Processing . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-5
3.2.15 etCO2 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-5
3.2.16 C.O. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-5
3.2.17 Power Management. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-6
3.2.18 Nurse Call Contacts . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-6
4 Troubleshooting
4.1 Power Problems. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-1
4.2 Display Problems . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-3
4.3 Alarm Problems. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-4
4.4 NIBP Problems . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-4
4.5 Temperature Problems . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-5
4.6 SpO2 Problems . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-6
4.7 etCO2 Problems . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-6
4.8 C.O. Problems (G40 Only) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-6
4.9 ECG/Respiration Problems . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-7
4.10 Recorder Problems . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-7
4.11 Performance Verification Testing . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-8
5 Repairing the G40 Patient Monitor
5.1 Service tools . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-1
5.2 Removing/Replacing the Batteries . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-1
5.3 Removing the AC power connector fuse . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-2
5.4 Removing the recorder . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-2
5.5 Separating the Front Case Assembly and the Rear Case Assembly . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-3
5.6 Disassembling the Front Case . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-5
5.6.1 Removing the ARM Module. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-5
5.6.2 Removing the LCD Display Assembly. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-6
5.6.3 Removing the Inverter . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-6
5.6.4 Removing the Alarm LED board . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-7
5.6.5 Removing the Keypad Board . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-8
5.6.6 Removing the Code Board . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-8
5.7 Disassembling the Rear Case . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-9
5.7.1 Removing the SpO2 Module. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-9
5.7.2 Removing the IBP and C.O. Module . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-10
Contents-2 G30/40 Patient Monitors Service Guide

5.7.3 Removing the Main Frame From the Rear Frame . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-11
5.7.4 Removing the ECG Module . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-12
5.7.5 Removing the CO2 module . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-13
5.7.6 Removing the NIBP Module . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-15
5.7.7 Removing the Main Board Module . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-16
5.7.8 Removing the AC/DC Power Module . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-16
5.7.9 Removing the Battery Board . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-17
5.7.10 Removing the AC Power Connector. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-18
5.7.11 Removing the I/O Module . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-19
5.8 Disassembling the Rear Frame . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-20
5.8.1 Removing the Fan and the Speaker Assembly . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-20
5.8.2 Removing the Handle Assembly . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-21
5.8.3 Installing the Handle Assembly . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-23
6 Repairing the G30 Patient Monitor
6.1 Service tools . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-1
6.2 Removing/Replacing the Batteries . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-1
6.3 Removing the AC Power Connector Fuse . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-2
6.4 To remove the recorder . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-2
6.5 To Separate the Front Case Assembly and the Rear Case Assembly . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-3
6.6 Disassembling the Front Case. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-5
6.6.1 Removing the ARM Module . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-5
6.6.2 Removing the Backlight Board. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-6
6.6.3 Removing the LED Display Assembly. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-6
6.6.4 Removing the Alarm LED Board . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-7
6.6.5 Removing the Keypad Board . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-8
6.6.6 Removing the Code Board . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-8
6.7 Disassembling the Rear Case . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-9
6.7.1 Removing the Main Frame From the Rear Frame . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-9
6.7.2 Removing the Connector Panel . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-11
6.7.3 Removing the SpO2 Module . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-14
6.7.4 To remove the IBP/TEMP Module. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-15
6.7.5 Removing the ECG Module . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-15
6.7.6 To remove the CO2 module . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-16
6.7.7 Removing the NIBP Module . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-16
6.7.8 Removing the Main Board Module . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-17
6.7.9 Removing the AC/DC Power Module . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-18
6.7.10 Removing the Battery Board . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-18
6.7.11 Removing the AC Power Connector Assembly . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-19
6.7.12 Removing the I/O Module . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-20
6.8 Rear Frame disassembly . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-21
6.8.1 Removing the Fan and the Speaker Assembly . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-21
6.8.2 Removing the Handle Assembly . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-22
7 Assembly Diagrams and Spare Parts
7.1 G40 Main Assembly Exploded Diagram . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-1
7.2 G40 Front Case Assembly and Parts. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-2
7.3 G40 Rear Frame Assembly and Parts . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-4
7.4 G40 Main Frame Assembly and Parts . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-5
7.5 G30 Main Assembly Exploded Diagram . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-8
7.6 G30 Front Case Assembly and Parts. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-9
7.7 G30 Rear Frame Assembly and Parts . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-10
7.8 G30 Main Frame Assembly and Parts . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-11
G30/40Patient Monitors Service Guide Contents-3

7.9 Spare Parts List . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-12
8 Electromagnetic Compatibility
8.1 Instructions for Use . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-1
8.2 Guidance and Manufacturer's EMC Declaration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-1
8.2.1 Electromagnetic Emissions for all Equipment and Systems. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-2
8.2.2 Electromagnetic Immunity for all Equipment and Systems . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-2
8.2.3 Electromagnetic Immunity for Equipment and Systems not Life-Supporting . . . . . . . . . . . . . . . . . . . . . . . . . 8-4
8.2.4 Recommended Separation Distances . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-5
8.2.5 Interference Test Results. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-5
Contents-4 G30/40 Patient Monitors Service Guide

1
General Introduction
This manual describes how to troubleshoot and repair the G30/G40 patient monitors. For more information
on maintaining, using, and cleaning the monitor during normal use, see the G30/G40 Patient Monitors
Instructions for Use.
1.1 Who Should Read This Guide

This guide is for qualified service personnel or technicians responsible for troubleshooting, repairing, and
maintaining the G30/G40 Patient Monitor (Service number is G30 : 865258, G40 : 865259).
A qualified service person or technician must be familiar with standard medical equipment installation
procedures, and familiar with current conventional technical terms used in this manual.
Before you start to service or repair the product, read this service guide and the G30/G40 Patient Monitors
Instructions for Use.
1.2 Repair Strategy

This service guide will help you determine whether a fault is a hardware or software problem.
Repair and/or replacement of individual board components is not supported and should never be attempted.
The disassembly, repair, or replacement of the G30/G40 Patient Monitor and its accessories without the
written authorization of Goldway will invalidate the warranty. The main replaceable parts are:
• Front case assembly
• Rear frame assembly
• ARM module
• LCD Display
• Inverter
• Keypad board
• Alarm LED board
• Code board
• Connectors panel
• SpO2 module
• TEMP module
• IBP/TEMP module
• IBP/TEMP/C.O. module (only for G40)
• ECG module
• NIBP module
• CO2 module
• System board
• AC power connector assembly
• AC/DC power module
• I/O module assembly
• Battery board
• Speaker
• Fan
• Recorder
G30/40 Patient Monitors Service Guide 1-1

Site Requirements
For diagrams and part numbers, see Chapter 7 "Assembly Diagrams and Spare Parts". For repair details, see
Chapter 5 "Repairing the G40 Patient Monitor" and Chapter 6 "Repairing the G30 Patient Monitor".
For tests after repairing, see "Testing and Inspection Guidelines" on page 2-1.
1.3 Site Requirements
1.3.1 Space Requirements

Situate the G30/G40 Patient Monitor in a place where the clinical staff is able to monitor the patient with
relative ease, with all patient connectors and controls readily available, and the displays clearly visible. The
location should also allow access for service personnel without excessive disruption and should have sufficient
clearance all around to allow air circulation.
For detailed physical specifications of the G30/G40 Patient Monitor, see Appendix B, “Specifications” in the
G30/G40 Patient Monitors Instructions for Use.
1.3.2 Environmental Requirements

The environment where clinicians will use the G30/G40 Patient Monitor should be free from vibration, dust
and corrosive or explosive gases. The ambient operating and storage conditions for the G30/G40 Patient
Monitor must be observed. If these conditions are not met, system accuracy could be affected and damage
might occur.
Table 1-1 Environmental Specifications
Environmental Specifications
Temperature Range Operating 10 oC to 40 oC (50 oF to 104 oF)
Storage and Transportation -20 oC to 55 oC (-4oF to 131 oF)
Relative Humidity Operating ≤80 % (non-condensing)

Storage and Transportation ≤95 % (non-condensing)
Barometric Pressure Operating 70 kPa to 106 kPa
Storage and Transportation 50 kPa to 106 kPa
1-2 G30/40 Patient Monitors Service Guide

G30/G40 Patient Monitors Overview
1.4 G30/G40 Patient Monitors Overview

The G30/G40 patient monitor collects the physiological signals of ECG, RESP, NIBP, SpO2,TEMP, IBP, C.O.
and CO2, and converts the above into digital data which is analyzed and displayed. You may not have all of
these functions, depending on the monitor configuration purchased.
1.4.1 Power Specifications

The following table describes the power specifications.
Table 1-2 Power Specifications
AC Power Parameter Specification

Mains power input 100 - 240V, 50Hz/60Hz
Power input 115VA
Fuse T1.6A, 250V
Battery Power Parameter Specification

Capacity Lead acid, 12V/2.3Ah per pcs
Charging time 8 hours
Typical operating time G30: 1.5 hours

G40: 2 hours (2 batteries)
Charge mode Automatic (with charge protection feature) when the

monitor is connected to an AC power source.
Discharge protection When the monitor is powered by battery, the monitor

powers off if the battery power is almost depleted.
1.4.2 Main Components

The monitor can contain these components:
• Main unit
• ECG
• RESP
• NIBP
• SpO2
• TEMP
• IBP
• C.O. (Only for G40)
• CO2
• Recorder
The following table lists the available configurations, the standard features in each monitor, as well as optional
features. In the table, a solid circle indicates a standard feature and a hollow circle, an optional feature.

G30/G40 Patient Monitors Overview
Table 1-3 Product Configurations
Parameter G30 G40

ECG (3, 5 leads) ● ●
TEMP1 ● ●
TEMP2
RESP ● ●
NIBP ● ●
SpO2 ● ●
CO2 ○ ○
IBP1 ○ ○
IBP2
C.O. N/A ○
Recorder ○ ○
Display Screen 10.4 inches 12.1 inches
Max. Number of Batteries 1 2
Ethernet Port ● ●
1.4.3 Indications for Use

The G30/G40 Patient Monitors are indicated for use by healthcare professionals whenever there is a need for
monitoring the physiological parameters of patients.
1.4.4 Intended Use

The G30/G40 Patient Monitors are intended for for monitoring, recording, and alarming of multiple
physiological parameters of adults, pediatrics and neonates in healthcare environments. Additionally, the
monitor is intended for use in transport situations and for connectivity to clinical networks.
1.4.5 Networking Capabilities

You can use the G30/G40 Patient Monitor along with other Goldway equipment to create a central monitoring
system that allows remote monitoring. The monitor communicates with the UT4800 Central Monitoring
System via an RJ45 port on the back of the monitor.
1.4.6 RJ45 Port

The monitor connects to the central monitoring system through the standard RJ45 port Ethernet interface.
When the monitor is connected to the network, a network symbol appears in the top right of the display. For
more information on connecting to the network, see your system manager or “Connecting to a network ” on
page 3-3 of the G30/G40 Patient Monitors Instructions for Use.

Before You Begin
1.4.7 HL7 Format

The G30/G40 Patient Monitor includes data export capability. The monitor can export data in HL7 format via
TCP/IP over Ethernet links to third party servers. The server stores the data or can forward it to the hospital
electronic medical record (EMR) system. You use the ethernet port on the back of the monitor for Ethernet
connections.
The G30/G40 Patient Monitor supports the parameters and alarm data export for standard monitor modules
such as ECG/RESP, HR/PR, SpO2, NIBP, IBP, and CO2. The Waveform data export for all standard monitor
modules and Cardiac Output/Multi-Gas export are not supported at present time.
1.5 Before You Begin

Before you start using the monitor:
1. Unpack the equipment and make sure that you have the following:
– 1 patient monitor
– Instructions for Use
– Service Guide CD
– AC power cord (country-specific)
– Set of accessories
If anything from the packing list is missing, immediately contact Goldway or a Goldway agent.
2. Keep the packaging for future transport or storage. If it is damaged, immediately contact the courier
company.
3. Examine the monitor for cleanliness and general physical condition. Make sure that the:
– Housing is not cracked or broken.
– Power plugs and cords are in good condition and plug prongs are not bent.
– External cables and accessories are in good condition and that the insulation is intact.
Caution If the equipment or packaging show signs of damage, do not use the equipment.
1.6 Installing the Monitor

Place and use the monitor in any appropriate location that conforms to the environmental specifications in the
G30/G40 Patient Monitors Instructions for Use. Ensure the following conditions exist in any area in which
you plan to use the monitor:
• Observation and operation of the monitor is convenient.
• The area is free from dust and corrosive or explosive gases.
• There is a minimum space of five centimeters from the top, bottom, and sides of the monitor to ensure
good ventilation and smooth heat dissipation.
Warning Never block the monitor’s air vent during operation.

Before Powering On
1.7 Before Powering On

Before turning the monitor on, check the available AC source as follows:
1. Ensure that the AC power source complies to any AC power regulations.
Note — Only connect the monitor to a power outlet with correct protective grounding. If no grounded power
is available, only use the monitor with internal batteries.
2. Connect the power cord to the monitor and to a single-phase AC power source.
3. Check that the power light on the front panel is yellow.
This means that the AC power is correctly connected.
Warning Personnel connecting additional devices to input and output connectors are responsible for system
compliance with the IEC 60601-1-1 standard. If you cannot determine the safety of the monitor when
combining it with another medical device, contact Goldway to ensure that the combined devices are safe
and will not cause electric shock or other hazards.
When safety (for example an electrical shock caused by the sum of current leakage) can not be determined
from the specific combination of the monitor and other medical devices, please contact service representative,
to ensure necessary safety.
1.8 Monitor and Accessories Inspection

1. Before turning on the power, check the monitor and accessories to make sure there is no damage and the
extension cables are correctly connected to the fittings.
2. Plug one end of the power cord into an AC power supply with a protective grounding wire. Plug the
other end into the power connector on the monitor. If the monitor is powered by batteries, make sure
enough power remains.
3. Power on the monitor and enter the main screen after the start-up screen.
4. Ensure that the patient cable and sensors are correctly connected.
5. Ensure that all settings like patient type, alarm limits, and so on, are correct.
6. Test the measurements and verify that the monitor is working correctly.
Warning Never attempt to open the monitor case. Only qualified personnel should service the monitor. Only use
the instructions in this guide to disassembly and repair the monitor.
Caution To maintain normal operation of the monitor, develop a good maintenance plan for periodic cleaning,
maintenance and service. For more information, see Chapter 2, Maintenance.

Setting Demo Mode
1.9 Setting Demo Mode

Demo mode lets you demonstrate the monitor without monitoring parameters. Demo mode does NOT
generates alarms when alarm settings are exceeded.
To set the Demo mode:
1. Press the Main Menu key on the front panel.
2. Rotate the navigation wheel to System menu and press the navigation wheel.
3. The System menu appears, and then rotate the navigation wheel to Demo then press the navigation
wheel.
4. The Logging On menu appears and rotate the navigation wheel to the Password, press the navigation
wheel. A password window appears. Enter the password (8727) by turning the wheel to select the digit,
and then press the wheel to save the first digit. Repeat this for the next three digits of the password.
5. Press OK.
1.10 Configuring a Network

You can use the G30/G40 Patient Monitors independently or with other Goldway equipment to create a central
monitoring system that allows remote monitoring. The monitor communicates with the Goldway Central
Monitoring System via the Ethernet port on the back of the monitor.
To enable a network:
1. Press the Main Menu key on the front panel to display the Main menu.
2. Rotate the navigation wheel to System and press the wheel.
3. Rotate the navigation wheel to Network Connection and press the wheel.
4. Rotate the navigation wheel to Network Port and press the wheel.
5. Rotate the navigation wheel to the X in the top right corner and press the wheel.
6. Repeat to return to the Main menu.
Rotate the navigation wheel to Exit to exit the Main menu.
To disconnect from a network:

1. Repeat above steps 1-3.
2. Rotate the navigation wheel to None and press the wheel.
4. Repeat to return to the Main menu.
Rotate the navigation wheel to Exit to exit the Main menu.
To configure the network connection:

1. Press the Main Menu key on the front panel to display the Main menu.
2. Rotate the navigation wheel to System and press the wheel.
3. Rotate the navigation wheel to Network Connection and press the wheel.
4. Rotate the navigation wheel to Network Port and press the wheel.
6. Rotate the navigation wheel to Network Setup and press the wheel.
A Network Setup window appears.

Configuring a Network
7. Check the IP configuration of the Goldway Central Monitoring System.

8. Set the G30/G40 monitor network as follows:
– Host IP: Must be different from other monitors connected to the Goldway Central Monitoring
System
– DVCP: No
– Server IP: Same as the Goldway Central Monitoring System
– Port: 8010, same as the Goldway Central Monitoring System
– Netmask: Same as the Goldway Central Monitoring System
– Gateway: Same as the Goldway Central Monitoring System
– Wireless: No
– Broadcast IP: N/A
– Mac ID: N/A
9. Rotate the navigation wheel to the OK and press the wheel to save the settings.

Upgrading the Software
1.11 Upgrading the Software

Before you begin a software upgrade, you need a USB stick, at least 1GB, with LED indicator.
To perform a software upgrade:
1. Format the USB stick with FAT or FAT 32.
2. Copy new version software to the USB stick.

3. Delete the version number from from all files listed as shown below.
4. Power on the G30/G40 patient monitor.

5. Press the Main Menu key and press the navigation wheel to select System.
6. Rotate the navigation wheel to About... and press the wheel.
7. Record the current software version.
8. Power off the G30/G40 patient monitor.
9. Insert the USB stick into the monitor.
10. Power on the monitor.
The system software will upgrade to the new version automatically. The USB stick LED indicator will blink
during the update.
11. Power off the monitor when the LED on the USB stick stops blinking. Remove the USB stick.
12. Repeat steps 4-6 to check software version.
13. Reset the MAC ID immedicately.
The software upgrade is complete.
Warning Before updating the software, record the MAC ID first. After software updating, re-set the MAC ID
according to the record immediately.

Upgrading the Software

2
Maintenance
This chapter describes how to inspect and maintain the G30/G40 patient monitors. It contains the testing
and maintenance procedures to ensure proper functioning of the monitor and accessories. The chapter also
contains information on preventive maintenance, performance assurance, and safety guidelines.
Perform the procedures as indicated in Table 2-1 Testing and Inspection Guidelines. The recommendations
in this table do not supersede local requirements.
For more information on how to clean and sterilize the monitor and accessories, see Chapter 15 “Cleaning
and Care” in the G30/G40 Patient Monitors Instructions for Use.
2.1 Manufacturer’s Responsibility

If hospital staff does not follow and adhere to the maintenance plan, which can lead to monitor inaccuracy,
as well as patient or operator hazard, the manufacturer shall not undertake any responsibility unless
otherwise agreed by both parties.
2.2 Testing and Inspection Guidelines

The following table lists the tests that Goldway requires to be completed after performing monitor
installations, repairs, or software upgrades.
Table 2-1 Testing and Inspection Guidelines
After... Complete These Tests...

Installing or exchanging a monitor Visual Test
Power Supply Test
Display Test
Upgrading the software Visual Test

Power Supply Test
Display Test
Opening the monitor for any reason Power Supply Test

Display Test
Speaker Test
All safety tests
Replacing any internal parts Power Supply Test

All safety tests
Display Test (front case assembly parts)
Applicable performance verification test
Connecting to central monitoring system Networking Test
Replacing recorder Recorder Test
G30/G40 Patient Monitors Service Guide 2-1

Recommended Frequency
2.3 Recommended Frequency

Perform the test procedures at the recommended frequency outlined in Table 2-2.
Caution The frequencies specified in the following table do not supersede local requirements. Always perform
locally required testing and the testing outlined in the table.
Table 2-2 Recommended Frequency
Suggested Testing Frequency

Preventive Maintenance
NIBP calibration Once a year, or more often if specified by local laws.
Microstream CO2 calibration First calibration at 1,200 hours of continuous use.

After first calibration, once a year or after 4,000 hours-
whichever comes first. Perform following any
instrument repairs or the replacement of any instrument
parts. Replace entire CO2 module after 20,000 hours
continuous use.
Performance
ECG Test Once a year, or if you suspect the measurement is

incorrect.
Respiration Test
Temperature Test
IBP Test
Pulse SpO2 Test
C.O.Test (BT and TI, G40 Only)
NIBP Test and Calibration
CO2 accuracy Once a year.
Safety Test (In accordance with IEC 60601-1)
• System enclosure leakage current Once every year and after repairs where the unit has
been opened (front and back separated) or the monitor
• Ground integrity
has been damaged by impact.
• Patient leakage current
2.4 Required Test Equipment

The following table lists the additional test equipment that you need to perform each of the tests in this
chapter. Many of these tests also use the standard accessories that are shipped with the monitor. Multi-
functional simulator, ECG trunk cable, 5-lead ECG lead set, blood pressure cuff and host, TEMP probe, digital
pressure meter, SpO2 simulator and SpO2 sensor etc.
2-2 G30/G40 Patient Monitors Service Guide

Required Test Equipment
Table 2-3 Required Test Equipment
To Perform This Test... You Need...

Visual Test None
Power Supply Test None
Display Test None
Speaker Test None
ECG Test Patient simulator

ECG trunk cable and lead set
Respiration Test Patient simulator

ECG trunk cable and lead set
Temperature Test MPS450 patient simulator (with 0.1oC or 0.2oF)

TEMP test cable 4G-450 (p/n: 453564310241)
IBP Test MPS450 Patient simulator

IBP test cable 4G-450 (p/n: 453564310231)
medSim 300B patient simulator
IBP test cable 4G-300B (p/n: 453564310211)
Pulse SpO2 Test Adult SpO2 sensor
C.O.Test (BT and TI, G40 Only) MPS450 simulator

Cardiac output adapter box
NIBP Test and Calibration Reference manometer (includes hand pump and valve),
accuracy 0.2% of reading
Expansion chamber (volume 500 ml +/- 10%)
Appropriate tubing
Microstream CO2 Calibration Standard tools, such as screwdriver, tweezers

• Electronic flow meter
• Gas calibration equipment:
– Cal gas (5% CO2)
– Cal gas flow regulator
– Cal tube
IBP Calibration IBP cable
Networking Test None
Electrical Safety Test Safety Tester and Multimeter
Recorder Test Print paper

Test Recording
2.5 Test Recording

Authorized Goldway personnel report test results back to Goldway to add to the product development
database. Hospital personnel, however, do not need to report results. The following table describes what to
record on the service record after you complete the tests in this chapter.
Table 2-4 Testing Record
Test What to Record

Visual Test V:P1 or V:F2
Power Supply Test PS:P or PS:F
Display Test V:P or V:F
Speaker Test S:P or S:F
ECG Test ECG:P or ECG:F
Respiration Test R:Por R:F
Temperature Test T:P or T:F
IBP Test IBPT:P or IBPT:F
Pulse SpO2 Test SpO2:P or SpO2:F
C.O.Test (BT and TI, G40 Only) CO:P or CO:F
NIBP Test NIBP:P or NIBP:F
NIBP Calibration NIBP:P/X31/X2/X3 or

NIBP:F/X1/X2/X3
Microstream CO2 Calibration CO2C:P or CO2C:F
IBP Calibration IBPC:P or IBPC:F
Networking Test N:P or N:V
Safety S(1):P/X1/X2 or
S(1):F/X1/X2
S(2): P/X1 or
S(2): F/X1
S(3): P/X1 or
S(3): F/X1
1. Pass
2. Fail
3. X= Measured value as defined in tests in this chapter

Performance Verification Tests
2.6 Performance Verification Tests

This section details the periodic maintenance recommended for the monitor, transducer and accessories.
Service personnel must inspect the monitor thoroughly and verify performance before the monitor is put into
service and every 12 months, or whenever necessary thereafter.
2.6.1 Visual Test

To perform the visual test:
1. Inspect the system for obvious signs of damage (example: cracks, cuts, or breakage).
2. Check all external cables and accessories (example: cuts, kinks, wrong connections).
3. Ensure that all markings and labeling are legible.
4. Check for any obstructions to mechanical parts.
The expected test result is that the system has no obvious signs of damage or obstruction.
2.6.2 Power Supply Test

To perform a monitor power supply and battery test:
1. Plug the monitor into an AC power outlet and apply power to the monitor.
2. The power LED should glow in one of the following colors:
– Green: the monitor is powered on and working normally.
– Yellow: the monitor is connected to AC power but not turned on.The internal battery is charging.
3. Unplug the AC power cord.
4. Verify that the power LED is green and a battery icon displays in the status box on the screen.
5. Perform an ECG test.
6. Reconnect the monitor to AC power and start the tests.
The power supply test is complete.
2.6.3 Display Test

To perform the display test:
1. Power on the G30/G40 Patient Monitor.
A start-up image appears.
2. Verify the image can be clearly displayed on the monitor, no blur, no distortion.
The display test is complete.
2.6.4 Speaker Test

To perform the speaker test:
1. Turn on the G30/G40 Patient Monitor.
2. Press the Main Menu button.
3. Rotate the navigation wheel to Vol & Light and press the wheel.
4. Rotate the navigation wheel to Alarm Volume and press the wheel.
5. Rotate the navigation wheel to adjust the alarm volume.
You should hear a tone from the speaker. The speaker test is complete.

2.6.5 ECG Test

To perform the ECG test, set the ECG simulator to: Heart rate: 80bpm; ECG gain: 1mV
1. Connect one end of the ECG cable to the ECG connector on the monitor and the other end to the
simulator.
2. Confirm that the patient simulator has been properly connected to the monitor. Ensure that the: ECG
lead II is displayed in the ECG channel, without noise. Heart rate display: 80 ± 2bpm. When R wave
appears, you can hear a “beep”.
3. Check every ECG lead to see if there is any ECG waveform and noise interference.
4. Adjusting ECG gain to 2mV, observe if there is any change in ECG waveform.
5. Unplug the RA from simulator, and then observe if the screen prompts “lead off”.
6. Reconnect RA lead.
7. Set 1mV calibration in the ECG setting menu, and observe if a 1mV calibration square wave is
overlapped over the ECG waveform.
The ECG test is complete.
2.6.6 Respiration Test

To perform the respiration test:
1. Connect the ECG cable to the ECG connector.
2. Set the simulator as follows: respiration baseline resistance: 500 Ohm, Respiration Delta R: 0.5 Ohm,
Respiration lead: I or II. Respiration rate: 30rpm
3. Set the monitor respiration lead to be RA-LA or LL-RL and set the respiration waveform channel.
4. Ensure that the respiration parameter area displays a reading of 30 ± 2rpm, and that the waveform
channel displays a respiration waveform.
5. Change the monitor respiration lead and repeat step 4.
6. Unplug the ECG cable.
The respiration test is complete.
2.6.7 Temperature Test

To perform the temperature test:
1. Connect the patient simulator to the temperature connector on the monitor through TEMP test cable.
2. Configure the patient simulator to 37 oC (98.6 oF).
3. Wait for the monitor to display the static temperature value.
4. The value should be 37 oC ± 0.1 oC (98.6 oF ± 0.18 oF).
5. If the value is not within tolerance, see "Temperature Problems" on page 4-5.
The temperature test is complete.
2.6.8 IBP Test

To perform the IBP test:
1. Set the simulator to: IBP output ATM.
2. Connect the IBP test cable to the IBP1 socket on the simulator and the other one to IBP1 socket on the
monitor.
3. Reset the monitor by resetting the IBP setting.
4. Select ART. Check if there is IBP measurement in the IBP area of the monitor, and also check if the IBP
waveform is shown in the relevant channel (the channel should be set in settings)

5. Change the IBP output of the simulator to 200mmHg.

6. Verify that the number on the screen is 200 ± 4mmHg (0.53kPa), whichever is greater.
7. Unplug the cable between the monitor and the simulator.
The IBP test is complete.
2.6.9 Pulse SpO2 Test

To perform the SpO2 test:
1. Adjust SpO2 simulator to X%.
2. Connect an adult SpO2 transducer that you know to be working correctly to the SpO2 connector on the
monitor. Ensure that the red LED in the sensor in the transducer is lit.
3. Connect the other end of the transducer to SpO2simulator.
4. Verify that the SpO2 value displayed on the monitor is X ± 2%.
The SpO2 test is complete.
2.6.10 C.O.Test (BT and TI, G40 Only)

To perform the C.O. test:
1. Connect the cardiac output adapter box to MPS450 simulator.
2. Connect one end of the C.O. cable to the C.O. connector, and the other end to the cardiac output box.
3. Connect the injection temp. sensor to the C.O. cable.
4. Power on the monitor.
A BT reading will be displayed on monitor’s screen.
5. Verify that the BT value displayed on the monitor is 37 ± 0.1oC.
The BT test is complete.
6. Rotate the navigation wheel to BT and press the wheel.
A Cardiac Setup window appears.
7. Rotate the navigation wheel to C.O. Measurement and press the wheel.
A C.O. Measurement window appears.
8. Rotate the navigation wheel to Setting and press the wheel.
A Setting window appears.
9. Rotate the navigation wheel to Injectate Mode and press the wheel.
10. Rotate the navigation wheel to Auto and press the wheel.
11. Rotate the navigation wheel to OK and press the wheel.
12. Rotate the navigation wheel to Start and press the wheel.
A TI reading will be displayed on monitor’s screen.
13. Verify that the TI value displayed on the monitor is approximately ambient temperature.
The TI test is complete.
14. Rotate the navigation wheel to Cancel and press the wheel.
15. Rotate the navigation wheel to Setting and press the wheel.
A Setting window appears.
16. Set the following items:
– Injectate Mode: Manual
– Catheter: 131HF7

– Injectate Vol.: 10cc

– Injectate Temp.: 0oC (32oF) or 24oC (75.2oF)
– Constant. : 0.542 (0oC) or 0.595 (24oC)
17. Rotate the navigation wheel to OK and press the wheel.
18. Adjust the simulator to X l/m, 0oC or 24oC.
Note — For more information on how to setup the MPS450, refer to the MPS450 Operations Manual.
19. Rotate the navigation wheel to Start and press the wheel.
20. Press the RUN button on the simulator.
A C.O. reading will be displayed on monitor’s screen.
21. Verify that the TI value displayed on the monitor is X l/m ±10%.
The C.O. test is complete.
2.6.11 NIBP Test and Calibration

Before you start, see "Required Test Equipment" on page 2-2 for a list of the equipment that you need to
perform this test.
Always check to see if the cuff or hose has a leak. Replace the cuff or hose as necessary. If a pressure reading,
when compared with a precise blood pressure meter, differs by more than 3% (beyond the range of ±3mmHg),
the monitor needs pressure calibration. Authorized personnel can perform the required calibrations.
These tests check the performance of the non-invasive blood pressure measurement. Perform each of these
NIBP checks and procedures when checking the NIBP unit:
• NIBP accuracy
• NIBP calibration procedure (if required)
• NIBP overpressure valve
To perform the NIBP accuracy test:
1. Connect the manometer and the pump with tubing to the NIBP connector on the G30/G40 Patient
Monitors.
2. Connect the tubing to the expansion chamber (500ml cylinder).
Figure 2-1 Connect the Tubing
3. Press the Main menu button. The Main Menu window appears. Rotate the wheel to the System button,
press the wheel.
4. Rotate the wheel to the System Maintenance .... Enter this menu.

5. Rotate the wheel to the Pressure Test. Press the wheel to start test.
6. Squeeze the manometer pump and apply a pressure of 50mmHg.
7. Note the pressure displayed in the NIBP Test window and record this result as X1 (see Test
Recording). It should be 50mmHg +/- 3mmHg.
8. Squeeze the manometer pump to apply a pressure of 250mmHg to the monitor.
9. Note the pressure displayed in the NIBP Test window and record this result as X2. The pressure in the
NIBP Test window should be 250mmHg +/- 3mmHg.
10. Press the NIBP button to stop the test.
If the difference between the manometer and displayed values is greater than 3mmHg, calibrate the monitor. If
not, skip to To Test the Overpressure.
2.6.11.1 To Test the Overpressure
press the wheel.
2. Rotate the wheel to the System Maintainence .... Enter this menu.
3. Rotate the wheel to the Pressure Test. Press the wheel to start test.
4. In the Adult,squeeze the manometer pump and apply a pressure of 290mmHg.
5. Verify the valves open, releasing the pressure on the manometer.
6. In the Neo., squeeze the manometer pump and apply a pressure of 150mmHg.
7. Verify the valves open, releasing the pressure on the manometer.
8. If you do not get the expected result see Chapter 4 “Troubleshooting”.
The overpressure test is complete.
2.6.11.2 To Calibrate the NIBP
press the wheel.
2. Rotate the wheel to the System Maintainence .... Enter this menu .
3. Rotate the wheel to Pressure Compensation. Press the wheel. The Pressure Compensation window
appears.
4. Rotate the wheel to select the appropriate value (Vadj).
5. Exit.
The calibrate test is complete.
2.6.12 Microstream CO2 Calibration

To check the calibration of the CO2 gas measurement:
1. Press the Param Menu key; rotate the navigation wheel to CO2 Setup, and press the wheel. The CO2
Setup menu appears.
2. Rotate the wheel to the Work Mode button and press the wheel. The Work Mode menu appears.
3. Rotate the wheel to the Work Mode button and press the wheel, rotate the wheel to the Standby, press
to exit.
4. Rotate the wheel to the CO2 Calibration button and press the wheel, the CO2 Calibration window
appears.
5. Connect one end of the Filter Line tubing to the CO2 inlet on the monitor; leave the other end
unconnected.
6. Connect the other end of the Filter Line tubing to the gas controller equipment inlet with a 5% gas
concentration.

Electrical Safety Test
7. Open the valve on the gas controller equipment to allow 5% CO2 gas to flow into the monitor.
8. In the CO2 Calibration window, rotate the wheel to the Two-Point Calibration. Press the wheel to
start calibration. The calibration message is displayed in the CO2 Calibration window.
Note — The calibration may take up three minutes to complete.
9. If calibration is successful, rotate the wheel to the Exit to leave the test. If not, calibration again. If
calibration is still not successful, replace the CO2 module.
2.6.13 IBP Calibration

To calibrate the IBP:
1. Connect one end of the IBP accessory to the IBP inlet on the monitor; leave the other end unconnected.
2. Press the Param Menu key; rotate the navigation wheel to IBP1 Setup and press the wheel. The IBP1
Setup menu appears.
3. Rotate the wheel to the IBP Calibration. Press the wheel to start calibration to atmospheric pressure.
Note — The IBP calibration can take up several seconds to complete.
4. Repeat the above steps to calibrate the IBP2.

If IBP2 can not be calibrated, do the calibration again. If IBP2 still can not be calibrated, replace the IBP
module.
2.6.14 Networking Test

Network the monitor with the UT4800 Central Monitoring System. Check that the ECG waveform displayed
on the monitor is properly displayed on the Central Monitoring System display.
2.7 Electrical Safety Test

Electrical safety test inspects whether the monitor has potential hazards to patients or operators.
In order to establish a systematic maintenance plan, we recommend all safety tests and records shall be made
under the following circumstances: Upon reception of the monitor, every year, and the monitor is opened for
repair.
Use the following safety test procedures for verifying safe installation or service of the monitor. The setups
used for these tests and the acceptable ranges of values are derived from local and international standards but
may not be equivalent. These tests are not a substitute for local safety testing where it is required for an
installation or a service event. If using the Metron Safety tester, perform the tests in accordance with your local
regulations, for example in Europe use IEC60601-1/IEC60601-1-1. The Metron Report should print results
with the names listed below, together with other data.
The monitor safety tests include:

• System Enclosure Leakage
• Ground integrity
• Patient leakage current with mains voltage

2.7.1 System Enclosure Leakage

S(1) Part 1: System Enclosure Leakage Current - NC (normal condition)
Expected Test Results:

Normal condition maximum leakage current x1 ≤ 100μA
This measures leakage current of exposed metal parts of Instrument under Test (IUT) and between parts of the
system within the patient environment; normal and reversed polarity using S2.
Safety test according IEC 60601-1 / UL60601-1.
S(1) Part 2: System Enclosure Leakage current - Single Fault (open earth)

Single Fault maximum leakage current x2 ≤ 500μA (IEC 60601-1)≤ 300μA (UL60601-1) This measures
leakage current of exposed metal parts of Instrument under Test (IUT) with Protective Earth (PE) open circuit
(S4 = open) and between parts of the system within the patient environment; normal and reversed polarity
using S2.

2.7.2 S(2) Protective Earth Continuity

With mains cable, maximum impedance x = 100 mOhms (IEC 60601-1 and UL60601-1)
This measures impedance of Protective Earth (PE) terminal to all exposed metal parts of Instrument under Test
(IUT), which are for safety reasons connected to the Protective Earth (PE). Test current 25 Amp applied for 5
to 10 seconds.
2.7.3 Patient Leakage Current with Mains Voltage

S(3) Patient Leakage current - Single Fault Condition (S.F.C.) mains on applied part

Maximum leakage current, x = 50μA @ 250V (IEC60601-1 and UL60601-1)
Measures patient leakage current from applied Part to earth caused by external main voltage on applied Part
with switch S5 open and closed. Each polarity combination possible is tested using S2 and S6. This test is
applicable for every measurement input.

Recorder Test
2.8 Recorder Test

To test the recorder, you load paper and press the Print key to start printing. For information on loading the
paper and printing, see the G30/G40 Patient Monitors Instructions for Use.

Recorder Test

3
Theory of Operation
This chapter introduces system theory of operation of G30/G40 Patient Monitors.
3.1 System Configuration
3.2 Theory of Operation

This chapter contains a high-level overview of the theory of operation of some major functional
components of the G30/G40 Patient Monitors.
3.2.1 System Overview

This chapter contains a system overview for the G30/G40 Patient Monitors, including a high-level block
diagram. This block diagram shows major components of the monitor, including the power supply, NIBP
control, SpO2 and CO2 processing, and microcontroller etc., The monitor is a full function monitor for use
on adult, pediatric, and neonatal patients. The functions performed by the system include:
• Monitoring patient ECG, heart rate and respiration rate
• Blood pressure
• Blood oxygen saturation
• Carbon dioxide
• Cardiac output
• Temperature
In addition to monitoring and displaying the status of physiological parameters, the monitor performs
various microprocessor-programmed analytical functions, including:

Theory of Operation
• Creating both visual and audible alarm signals when settings are violated
• Creating and displaying warning messages when conditions are detected that would degrade or prevent
valid measurements
• Creating and displaying trend waveforms or tabular data
• Providing ECG Analog Output.
• Providing input to an optional recorder for printout of current or trend waveforms or tabular data
The G30/G40 Patient Monitor operates from either an AC power source or battery power. The monitor charges
the battery when powered by AC.
3.2.2 Block Diagram Components

The G30/G40 Patient Monitors contain several major blocks, including:
• Functional module (including ECG, SpO2, NIBP, IBP/TEMP, CO2, C.O.(optional for G40), and
Recorder)
• ARM module
• Main Board assembly
• I/O module assembly
3.2.3 ARM Module

The ARM module contains these components:
• ARM9 microprocessor
• Flash memory
• SDRAM
• Silicon Motion Multimedia Processor
• Connectors
– Display assembly
– Main Board assembly (wire to Main Board assembly)
– I/O module assembly (wire to I/O module assembly)
• USB
• Voltage regulator
3.2.4 System Module

The system board contains a DC/DC voltage converter, which provides power and communication to:
• IBP
• ECG
• SpO2
• NIBP
• IBP/Temp
• CO2
• C.O. (optional for G40)
• Recorder
• ARM board
• Inverter / Backlight Board
• Speaker

Theory of Operation
• Keys
• Battery charging module
3.2.5 I/O Module Assembly

The output interface board provides the connector socket for the following applications:
• Display output port
• Nurse call port
• USB Port
• Ethernet port
• ECG analog output port
• Connection to the ARM Module
3.2.6 Speaker
The speaker is driven by an amplifier. The speaker provides the monitor’s audio during alarm conditions. The
microprocessor outputs different audio tones specified by different alarm priorities and conditions.
3.2.7 Recorder
The recorder contains the following functions:
• Motor (paper drive) and driver circuitry
• Selectable print speed
– 12.5mm/s, 25mm/s, Auto
• Selectable channel waves to print
Print head control logic is implemented on the Main Board. The microprocessor sends data to the recorder via
a serial port.
3.2.8 AC/DC Power Module

The G30/G40 Patient Monitor contains a medical grade power supply module and circuitry that converts AC
(100-240V) to DC (15V). Power consumption is 115 VA.
3.2.9 Keys and Navigation Wheel

The keys and navigation wheel generate pulses to the Main Board assembly during use, and the Main Board
assembly encodes the message to the ARM module, the patient monitor can respond to all kinds of operations.
3.2.10 NIBP Processing

The NIBP assembly and circuitry contain these elements:
• Pump
• Valves (2-valve system of dump and safety valve)
• Pressure measurement and control circuitry
Pressure data is converted to digital format and conveyed to the processor. The NIBP pump uses an
oscillometric method that employs stepwise pressure deflation. Pump software eliminates most ambient noise
and motion interference. Applications are neonatal, pediatric and adult patients. The blood pressure range is:
Systolic, 30-254 mmHg and Diastolic, 10-220 mmHg. Accuracy is Maximum Mean Error ±5 mmHg with
Max. Standard Deviation 8 mmHg.

Theory of Operation
NIBP processing uses an oscillometric technique to provide needed measurements at selected intervals. This
technique uses an inflatable sphygmomanometer cuff similar to those used by clinicians in routine
measurements. A motorized pump inflates the cuff to approximately 170 mmHg (adult mode) initially, at
which point the pressure effectively stops the flow of blood. Then, under monitor control, the pressure in the
cuff is gradually reduced, while a pressure transducer detects the pressure and transmits the parameter signal to
the NIBP input circuitry. As the pressure is reduced, blood flows in the previously occluded artery, and
changes the measurements made by the transducer. The point at which oscillation increases sharply is defined
as systolic pressure. As the cuff keeps deflating, the oscillation amplitude increases to maximum, and then
decreases. The peak oscillation amplitude is defined as the mean arterial pressure. The point at which the
system detects a rapid decrease in oscillation is defined as the diastolic pressure.
3.2.11 SpO2 Processing

SpO2 is a measurement of oxygen saturation in the blood that uses an optical spectrophotometry technique. It
is based on the differences in the absorption of red and Infrared light by oxygenated and de-oxygenated
Hemoglobin. A pulse oximeter passes red and infrared light into an arteriolar bed and measures changes in
light absorption during the pulsatile cycle. The light sources are red and infrared light emitting diodes (LEDs).
A photo diode provides detection. To identify the oxygen saturation of arterial hemoglobin, the G30/G40
Patient Monitor use the pulsatile nature of arterial flow. During systole, a new pulse of arterial blood enters the
vascular bed, and both blood volume and light absorption increase. During diastole, blood volume and light
absorption reach their lowest point. The measurement is based on the difference between maximum and
minimum absorption, focusing on the pulsatile arterial blood. In addition to the oximetry function, the
measurement can also provide the heart rate.
3.2.12 ECG Processing

The monitor measures the patient's ECG signals by sensing the varying potential difference between several
points at the skin surface which respond to the electro-chemical actions of the muscular activity of the heart.
Up to five electrodes are attached to the patient’s body. The varying potentials at these locations are sent to the
ECG circuitry. These signals are amplified and filtered and then digitized before being transmitted to the
microprocessor.
The microprocessor executes algorithms to:
• Calculate the ECG data
• Compute the heart rate
• Perform the ARR and ST analysis
• Detect a lead-off condition if one of the electrode connections is disrupted
• Detect the presence of pacemaker signals within the QRS waveform complex of the ECG
• Generate an analog output for external use with defibrillators
Note — The ECG analog output is available at a connector on the back of the monitor.
3.2.13 IBP Processing

The invasive blood pressure (IBP) measurement produces real-time waveforms and numeric values for
systolic, diastolic, and mean arterial blood pressure. IBP measurements use an A/D converter. An isolation
transformer and opto-coupler provide the required isolation between isolated and grounded chapters of the
monitor. Software algorithms filter typical artifacts like respiratory variation and pressure changes caused by
flushing the line or drawing blood samples.

Theory of Operation
3.2.14 Temperature Processing

Resistance temperature detectors (RTDs) measure temperatures using the physical principle of the positive
temperature coefficient of electrical resistance of metals. The hotter they become, the larger – or higher –the
value of their electrical resistance. The advantage is stable outputs for long periods of time, ease of
recalibration, and accurate readings over relatively narrow temperature spans. The monitor’s input circuitry
conditions and processes the signal to drive the numeric display.
3.2.15 etCO2
The etCO2 module contains a:
• CO2 sensor assembly
• Flow system, including pump
• Signal processing PCB and peripherals
• Serial interface
• Power supply
• FRS (FilterLine Recognition Safeguard) to identify correct usage of a MicroStream FilterLine®
• Input gas connector with FRS interface
The G30/G40 Patient Monitor uses the Microstream® sidestream etCO2 method to measure carbon dioxide
(CO2). The sidestream measurement method samples the respiratory gas with a constant flow from the
patient’s airway and analyzes it with a remote CO2 sensor built into the monitor.
The CO2 measurement produces:
• A CO2 waveform
• An end tidal (etCO2) value: the CO2 value measured at the end of the expiration phase
• An inspired minimum CO2 (InCO2) value: the smallest value measured during inspiration
• An airway respiration rate (awRR): the number of breaths per minute, calculated from the CO2
waveform
All infrared gas measuring instruments, including the CO2 module, consist of a radiation source, a cell through
which samples of gas flow and a detector that transmits a signal related to the intensity of the radiation that is
detected. The quantitative aspects of photometric measurement are stated by the Beer-Lambert law:
A = Log (Io/I) = εlc
Under carefully controlled conditions at a select absorption band, the absorbency of a sample (A) is
proportional both to the concentration of the sample (c) and the depth of the absorbing layer (l). The molar
extinction coefficient (ε) is a wavelength dependent constant characterizing the sample. (Io) is the light
intensity at zero absorbency and (I) is the light intensity after some of the light is absorbed by the sample. The
CO2 module, as most continuous monitors of carbon dioxide, uses a non dispersive infrared (NDIR) light
source. All CO2 monitoring instruments, except those manufactured by Oridion, that use a NDIR infrared light
source, use the broad band energy from a black-body source. A mechanical chopper modulates the light beam
and makes possible the monitoring of the sample, reference and dark signals from which the concentration of
carbon dioxide can be determined. The CO2 module uses the energy generated by an infrared source that
includes a proprietary gas filled lamp and driver circuit. This energy contains only specific wavelengths which
match the absorption bands of the CO2. The CO2 module's infrared source is electronically modulated by the
driver circuit.
3.2.16 C.O.
The Cardiac Output (C.O.) measurement invasively measures cardiac output and other hemodynamic
parameters using a technique called thermodilution. This can be used to determine the flow rate of a system by
introducing a cold solution into the system and measuring the resulting drop in the temperature at a
downstream site. Two temperature sensors are used to measure the C.O. value. One is used to measure the
temperature of the cold solution, and the other is used to measure the temperature of the human blood. This
temperature change is displayed as a curve and the monitor calculates the C.O. value from this curve. As

Theory of Operation
cardiac output varies continuously, a series of measurements must be carried out to achieve a reliable C.O.
average value. Always use the average of multiple thermodilution measurements for therapy decisions.
3.2.17 Power Management

The G30/G40 Patient Monitor contain a medical grade power supply module and circuitry that converts AC
(100-240V) to DC (15V). Power consumption is 115 VA.
The power management module contains:
• Lead-acid batteries
– 12 V, 2.3 AH
• Battery charger
• DC/DC converter
The power management circuitry charges the battery through a battery charger(s). Both the battery(s) and the
AC/DC power module can power the system through several DC/DC converters that provide various voltage
outputs required by various chips. Isolated transformers provide the power to the front ends floating area.
3.2.18 Nurse Call Contacts

The nurse call alarm contacts are available through a 3.5mm, miniature insulated phone jack on the back of the
unit. The alarm contacts close (open) for any alarm condition detected by the monitor.
The alarm contacts are the three switching signals associated with a single pole, double throw relay:
• Normally open contact (NO)
• Common contact
• Normally closed contact (NC)
Contact Rating of:

NO = 1A @ < 25Vac
Common contact = 1A @ < 60Vdc
Isolation of 1.5kV

4
Troubleshooting
This chapter describes how to troubleshoot monitor problems. After using this chapter to diagnose a
problem, see Chapter 5, Repairing the G40 Patient Monitor and Chapter 6, Repairing the G30 Patient
Monitor to repair the monitor or to remove and replace a part or assembly.
4.1 Power Problems
Symptom Possible cause Action

I cannot turn on the The cord is unplugged or Ensure that the AC power cord is plugged into
monitor by AC. broken. an outlet.
The fuse is blown. Replace the fuse. See "Removing the AC power
connector fuse" on page 5-2 or "Removing the
AC Power Connector Fuse" on page 6-2.
The AC socket board has Replace the AC socket board. See "Removing
malfunctioned. the AC Power Connector" on page 5-18 or
"Removing the AC Power Connector
Assembly" on page 6-19 .
The AC/DC Power Check output voltage on AC/DC Power

Module has Module. If you do not capture 15 V, replace the
malfunctioned. AC/DC Power Module. See "Removing the
AC/DC Power Module" on page 5-16 or
"Removing the AC/DC Power Module" on
page 6-18 .
The DC power cable has Replace the AC connector.See "Removing the

malfunctioned. AC/DC Power Module" on page 5-16 or
"Removing the AC/DC Power Module" on
page 6-18 .
The main board module Ensure that the AC power cord is plugged into.
cable is unplugged or Replace the main board module cable. See
broken. "Removing the Main Board Module" on
page 5-16 or "Removing the Main Board
Module" on page 6-17.
The main board module is Replace the key&system module. See

The ARM board module Replace the ARM board module. See
has malfunctioned. "Removing the ARM Module" on page 5-5 or
"Removing the ARM Module" on page 6-5.

Power Problems

I cannot turn on the The battery or connector is Reseat both the battery and battery cable.
monitor by battery. loose.
The battery board has Replace the battery board. See "Removing the
malfunctioned Battery Board" on page 5-17 or "Removing the
Battery Board" on page 6-18.
The main board module Ensure that the AC power cord is plugged into.
cable is unplugged or Replace the main board module cable. See
The main board module is Replace the main board module. See
The ARM module has Replace the ARM module. See "Removing the
malfunctioned. ARM Module" on page 5-5 or "Removing the
ARM Module" on page 6-5.
The battery has run out. Charge the battery. For more information, see
"Removing/Replacing the Batteries" on
page 5-1 or "Removing/Replacing the
Batteries" on page 6-1.
The battery will not Replace the battery. For more information, see
charge. "Removing/Replacing the Batteries" on
page 5-1 or "Removing/Replacing the
Batteries" on page 6-1.
The inverter has Replace the inverter. See "Removing the

malfunctioned. Backlight Board" on page 6-6.
The backlight board has Replace the backlight board. See

malfunctioned Appendix , ?$paratext[ChapTitle(App)]>?
May be the display has Check the display, replace the display. See
malfunctioned. "Removing the LCD Display Assembly" on
page 5-6 or "Removing the LED Display
Assembly" on page 6-6.

Display Problems
4.2 Display Problems

Power is on, but the There is a bad connection Ensure that there is a proper connection between
monitor screen is blank with the backlight LCD the cable, LCD, backlight and Main board
module.
There is a bad LCD. Replace the Display assembly. See "Removing

the LCD Display Assembly" on page 5-6 or
"Removing the LED Display Assembly" on
page 6-6.
There is a bad inverter. Replace the inverter. See "Removing the

Inverter" on page 5-6.
There is a back backlight Replace the backlight board. See "Removing the
board. Backlight Board" on page 6-6.
The main board module Replace the main board module. See "Removing
has malfunctioned. the Main Board Module" on page 5-16 or
"Removing the Main Board Module" on
page 6-17.
The monitor displays The LCD cable is not Open the monitor and reseat the LCD signal
random/ distorted attached correctly cable.
graphics with a white
background. The LCD has Replace the Display assembly. See "Removing
malfunctioned. the Inverter" on page 5-6 or "Disassembling the
Rear Case" on page 6-9.
The main board module Replace the main board module. See "Removing
has malfunctioned. the Main Board Module" on page 5-16 or
"Removing the Main Board Module" on
page 6-17.
I turn on the monitor The ARM module has Replace the ARM module. See "Removing the
and the opening screen malfunctioned. ARM Module" on page 5-5 or "Removing the
and/or color bar starts, ARM Module" on page 6-5.
but then just hangs.
The monitor does not There is a bad connection Ensure that all connectors to the main board
respond to the to the main board module. module are seated correctly.
navigation wheel or
front panel buttons The monitor keypad or Replace the front case, See "Disassembling the
navigation wheel is Front Case" on page 5-5 or "Disassembling the
broken. Front Case" on page 6-5.

Alarm Problems
4.3 Alarm Problems

Audible alarms do not There is a bad connection Ensure that the connection to speaker is correct.
sound to the speaker.
The speaker is bad. Replace the fan & speaker assembly. See
"Removing the Fan and the Speaker Assembly"
on page 5-20 or "Removing the Fan and the
Speaker Assembly" on page 6-21.
There is a bad connection Ensure that all connectors to the main board
to the main board module. module are seated correctly.
4.4 NIBP Problems

The NIBP cuff does not The tube or cuff is kinked. Straighten the tube or cuff.
inflate
There is an air leak in the Replace the cuff and ensure that there is no air
air tube or cuff. leakage in the tube.
The NIBP module has not Reset the NIBP module case.
set in correctly.
The NIBP module has Replace the NIBP module. See "Removing the
malfunctioned. Main Board Module" on page 5-16 or "Removing
the NIBP Module" on page 6-16.

Temperature Problems

There are no NIBP Wrong cuff size or Use proper cuff size, ensure proper cuff
readings incorrect cuff placement. placement.
The tube is kinked or there Ensure that the tube is straight and not kinked.
is air leakage in the air Replace the cuff and ensure that there is no air
tube or cuff. leakage in tube.
There has been some Ensure that all external blood pressure reading
external problem. requirements are met and that the patient is not
moving excessively.
The NIBP module has not Reset the NIBP module case.
set in correctly.
The NIBP module has Replace the NIBP module. See "Removing the
malfunctioned. Main Board Module" on page 5-16 or "Removing
the NIBP Module" on page 6-16.
I am getting unreliable Wrong cuff size or Use proper cuff size, ensure proper cuff
NIBP readings incorrect cuff placement. placement.
There have been some Ensure that all external blood pressure reading
external problems. requirements are met and that the patient is not
moving excessively.
4.5 Temperature Problems

There are no The probe is off. Ensure that the temperature probe is connected.
temperature readings
The temperature is over Ensure that temperature readings are in the range
range. of 0oC-50oC.
The probe has Replace the temperature probe.

malfunctioned.
The Temperature module Replace the Temperature module. See

has malfunctioned. "Removing the IBP and C.O. Module" on
page 5-10 or "To remove the IBP/TEMP
I am getting unreliable The probe has Replace the temperature probe.

temperature readings malfunctioned.
The Temperature module Replace the Temperature module. See

has malfunctioned. "Removing the IBP and C.O. Module" on
page 5-10 or "To remove the IBP/TEMP

SpO2 Problems
4.6 SpO2 Problems

There are no SpO2 The SpO2 sensor has Replace the SpO2 sensor.
readings malfunctioned.
The SpO2 module has Replace SpO2 module. See "Removing the SpO2
malfunctioned. Module" on page 5-9 or "Removing the SpO2
The ARM module has Replace the ARM Module. See "Removing the
The SpO2 readings are There has been some Ensure that all external SpO2 reading
unreliable external problem. requirements are met and that the patient is not
moving excessively.
4.7 etCO2 Problems

There are no CO2 The CO2 module is Wait until initialization is complete.
readings initializing.
The CO2 tube is kinked. Check the tube to ensure that it is straight.
The CO2 module has Replace the CO2 module. See "Removing the
malfunctioned. CO2 module" on page 5-13 or "To remove the
CO2 module" on page 6-16.
The CO2 readings area The CO2 tube is kinked. Check the tube and make sure that it is straight.
unreliable
There have been some Ensure that all external CO2 reading
external problems. requirements are met and that the patient is not
moving excessively.
4.8 C.O. Problems (G40 Only)

There are no C.O. There are no TI or BT Replace the IBP/C.O. module. See "Removing
readings readings. the IBP and C.O. Module" on page 5-10.

ECG/Respiration Problems
4.9 ECG/Respiration Problems

There are no ECG The ECG leads are off. Ensure that the leads are connected.
readings
The ECG cable is broken. Ensure that the cable is in good working order.
The ECG 3/5 lead set is Correct the ECG configuration.

not configured correctly.
The ECG module has Replace the ECG module. See "Removing the
malfunctioned. ECG Module" on page 5-12 or "Removing the
ECG Module" on page 6-15.
I am getting unreliable The ECG leads are off. Ensure that the ECG leads are connected.
ECG readings
There has been some Ensure that all external ECG reading
external problem. requirements are met and that the patient is not
moving excessively. Ensure proper skin
preparation has been performed.
There are no respiration The respiration leads are Ensure that the respiration leads are connected.
readings off.
The ECG module has Replace the ECG module. See "Removing the
malfunctioned. ECG Module" on page 5-12 or "Removing the
ECG Module" on page 6-15.
The respiration There has been some Ensure that all respiration reading requirements
readings are unreliable external interference. are met and that the patient is not moving
excessively. Ensure that the correct ECG lead set
is being used.
4.10 Recorder Problems

The recorder paper is The paper is not installed Remove paper and reinstall correctly.
jamming correctly.
The recorder is using Use only the recommend recorder paper.

improper paper.
The recorder has a Reset or replace the recorder module.

mechanical problem.

Performance Verification Testing

The recorder does not The paper is out and/or the Install a new paper supply. Open the recorder
print recorder door is open. door, and then close it again.
The system does not Check the recorder’s physical connections.

recognize the recorder.
The recorder module has Replace the recorder module.

malfunctioned.
The main board has Replace the main board. See "Removing the
malfunctioned. Main Board" on page 5-11.
4.11 Performance Verification Testing

After repairing the monitor, Goldway recommends that you perform Performance Verification Testing. See
"Performance Verification Tests" on page 2-5 and "Electrical Safety Test" on page 2-10.

5
Repairing the G40 Patient Monitor
This chapter describes the procedures for disassembling and assembling the G40 Patient Monitor in order to
replace or repair defective assemblies/components.
5.1 Service tools

Only standard tools are required to perform service on this product.
Following tools are recommended:
• One Phillips screwdriver 5mm (at least 100mm long)
• One Phillips screwdriver 3mm
• One Flat-Head screw driver 5mm
• One Wire cutter
• One Long flat nose plier or Spanner
• One Hexagon Nut driver 5.5mm
5.2 Removing/Replacing the Batteries
Caution Before removing the battery, perform a monitor shutdown and disconnect the monitor from AC
power.
To remove the batteries:

1. Push the battery cover in the direction indicated on the cover.
2. Remove the batteries by using one thumb to push on the batteries, and your other thumb to rotate the
lock bar.

Removing the AC power connector fuse
5.3 Removing the AC power connector fuse

To remove the AC power connection fuse:
1. Use a flat-head screwdriver to lift the fuse holder away from AC power connector.
2. Pull out the fuse holder and remove and replace the fuse as shown.
3. To replace the fuse holder, push it back into the power connector until it snaps into the place.
5.4 Removing the recorder

To remove the recorder:
1. Open the recorder door.

Separating the Front Case Assembly and the Rear Case Assembly
2. Remove the paper roll, and remove the two M3X6 screws, round head with a 3mm Phillips head
screwdriver.
3. Use your thumbs to grip the inside walls of the recorder case and pull it straight out of the assembly and
remove the recorder connector cable.
Recorder
Connector Cable
5.5 Separating the Front Case Assembly and the Rear Case Assembly
To separate the front case assembly and the rear case assembly:
1. Turn the monitor over and remove the two M3×8 screws.

Separating the Front Case Assembly and the Rear Case Assembly
2. Remove the two M3×12 screws as shown.
3. Turn the monitor upright, the front case and the rear case are held by the notch buckle. Gently open the
monitor.
4. Use the wire cutter to remove the cable tie and unplug all connector cables to separate the front case
assembly and the rear case assembly.
LED Alarm Cable
Power Cable
Keypad Cable
Grounding Wire
ARM Cable

Disassembling the Front Case
5.6 Disassembling the Front Case

The front case assembly including following main components:
• ARM module
• LCD display assembly
• Inverter
• Alarm LED board
• Keypad board
• Code board
5.6.1 Removing the ARM Module

1. Remove the six M3x6 screws and the LCD connector cable.
LCD Connector Cable
2. Remove the ARM module.

5.6.2 Removing the LCD Display Assembly

To remove the LCD display assembly:
1. Remove the seven M3x8 screws.
2. Remove the LCD gently.
LCD Inverter
5.6.3 Removing the Inverter

To remove the inverter:
1. Remove the two M3x6 screws to remove the inverter shield.

2. Remove all connector cables.
LCD Driver
Cable
Inverter Control
Cable
LCD Driver
Cable
3. Use hexagon nut driver (5mm) to remove the two M3 nuts, .
4. Remove the inverter.
5.6.4 Removing the Alarm LED board

To remove the alarm LED board:
1. Remove the two M3x8 self-tapping screws.
2. Remove the alarm LED board.

5.6.5 Removing the Keypad Board

To remove the keypad board:
1. Remove the code board cable and the six M3x8 self-tapping screws.
2. Remove the keypad board.
5.6.6 Removing the Code Board

To remove the code board:
1. Remove the silicon key.
2. Unplug the navigation wheel cap.
Pull Upright
3. Use Hexagon nut driver to remove the nut and remove the code board.

Disassembling the Rear Case
5.7 Disassembling the Rear Case

The rear case assembly includes following main components:
• Main frame assembly:
– SpO2 module
– IBP and C.O. module
– ECG module
– CO2 module
– NIBP module
– System board
– AC/DC power module
– Battery charging board
– AC power connector assembly
– I/O module
• Rear frame assembly:
– Fan
– Speaker
5.7.1 Removing the SpO2 Module

To remove the SpO2 module:
1. Remove the two plastic M3X6 screws and the SpO2 connector cable.
SpO2 Connector Cable
2. Gently remove the SpO2 module.

5.7.2 Removing the IBP and C.O. Module

To remove the IBP and C.O. module:
1. Remove the four M3x6 screws.
2. Remove all connector cables.
IBP2 Connector Cable
IBP1 Connector Cable
C.O. Connector Cable
TEMP1/TEMP2 Connector
Cable
Caution Note the order of all connector cables. Especially IBP1 and IBP2 connectors.
3. Remove the IBP and C.O. module gently.

5.7.3 Removing the Main Frame From the Rear Frame

To remove the main frame from the rear frame:
1. Remove the five M3x6 screws and remove the fan and speaker cables as well
Speaker Cable Fan Cable
2. Remove the three M3x8 screws on the bottom.
3. Press the connector panel in the direction of the aarow and slide the connector panel out.

4. Separate the main frame and the rear frame.
Main Frame
Rear Frame
5.7.4 Removing the ECG Module

To remove the ECG module:
1. Remove the three M3X6 screws and all connector cables.
ECG Cable ECG Connector

Cable
2. Remove the ECG module gently.

5.7.5 Removing the CO2 module

To remove the CO2 module:
1. Remove the two connector cables and the four M3X6 screws.
CO2 Cable CO2 Connector Cable

2. Remove the CO2 tube and socket.
3. Remove the CO2 module gently.

To install the CO2 socket:

1. Install the tube to the outlet.
2. Install the fixed socket.
3. Set the socket into the connector panel, and rotate it anticlockwise.
4. Install the screws.

5.7.6 Removing the NIBP Module

1. Remove the NIBP cable and the four M3X6 screws.
NIBP Cable
2. Remove the four M3X6 screws.
3. Remove the NIBP module gently.

5.7.7 Removing the Main Board Module

1. Remove the eight M3x6 screws.
2. Remove the Main Board gently.
5.7.8 Removing the AC/DC Power Module

1. Remove AC power cable and DC power cable.
AC Power DC Power
Cable Cable

3. Remove the power module gently.
5.7.9 Removing the Battery Board

2. Remove the battery board gently.

5.7.10 Removing the AC Power Connector

1. Remove the two M3x4 flat head screws.
2. Use the long flat nose plier or spanner to remove the nut.
Nut
3. Remove the AC power connector gently.

5.7.11 Removing the I/O Module

1. Unplug the cables, remove the three M3x4 flat head screws.
2. Remove the module gently.
3. Remove the CRT cable and two M3x6 screws.
CRT Cable
4. Remove the I/O board.

Disassembling the Rear Frame
5. Use the Hexagon Nut driver to remove the two nuts.
6. Remove the CRT socket.
5.8 Disassembling the Rear Frame
5.8.1 Removing the Fan and the Speaker Assembly

1. Remove the white-clip M3x8 screw with washes and the four M3x6 screws.
M3x8
2. Remove the fan and the speaker.

5.8.2 Removing the Handle Assembly

To remove the handle assembly:
1. Remove the six screws at A, B, and C.
A
A
B C C B
B: M 3x6 screws
with washes C: M 3x8
A: M 3x25 screws Self-tapping
with washes Screws
2. Press the handle assembly and remove it.
3. Remove the handle fixing frame.

4. Remove the two M3x8 screws and washes.
5. Separate the front carry handle and the back carry handle assembly.
Back Carry Handle

Front Carry Handle Assembly
6. Remove the M3x8 screws and washes.
7. Remove the left and right pothook.
Back Carry Handle
Left Pothook Right Pothook

5.8.3 Installing the Handle Assembly

To install the handle assembly:
1. Install the handle fixing frame.
2. Install the two M 3x8 self-tapping screws and washes.
3. Install the handle assembly.

4. Install the two M 3x8 screws and washes.
5. Install the two M 3x25 screws and washes.

6
Repairing the G30 Patient Monitor
This chapter describes the procedures for disassembling and assembling the G30 Patient Monitor in order to
replace or repair defective assemblies/components.
6.1 Service tools

Only standard tools are required to perform service on this product.
Following tools are recommended:
• One Phillips screwdriver 5mm (at least 100mm long)
• One Phillips screwdriver 3mm
• One Flat-Head screw driver 5mm
• One Wire cutter
• One Long flat nose plier or Spanner
• One Hexagon Nut driver 5.5mm
6.2 Removing/Replacing the Batteries
Caution Before removing the battery, perform a monitor shutdown and disconnect the monitor from AC
power.
To remove the batteries:

1. Open the battery door.
2. Remove the batteries by using one thumb to push on the batteries, and your other thumb to rotate the
lock bar.

Removing the AC Power Connector Fuse
6.3 Removing the AC Power Connector Fuse

To remove a fuse in AC power connector:
1. Use a flat-head screwdriver to lift the fuse holder away from AC power connector.
2. Pull out the fuse holder and remove and replace the fuse as shown. To replace the fuse holder, push it
back into the power connector until it snaps into the place.
6.4 To remove the recorder

To remove the recorder:
1. Open the recorder door.

To Separate the Front Case Assembly and the Rear Case Assembly
2. Remove the two M3x6 screws.
3. Use your thumbs to grip the inside walls of the recorder case and pull it straight out of the assembly and
remove the recorder connector cable.
6.5 To Separate the Front Case Assembly and the Rear Case Assembly
To separate the front case assembly and the rear case assembly:
1. Turn the monitor over. Remove the two M4x8 screws and washes as shown.

To Separate the Front Case Assembly and the Rear Case Assembly
2. Remove the two M4x8 screws and washes.
3. Turn the monitor upright, the front case and the rear case are held by the notch buckle. Gently open the
monitor.
4. Use the wire cutter to remove the cable tie and unplug all connector cables to separate the front case
assembly and the rear case assembly.
Keypad Cable
I/O Cable
Backlight Board Cable
ARM Cable Grounding Wire
LED Connection
Cable

6.6 Disassembling the Front Case

The front case assembly including following main components:
• ARM module
• LCD display assembly
• Backlight board
• Alarm board
• Keypad board
• Code board
6.6.1 Removing the ARM Module

1. Remove the cable tie, the six M3x6 screws and the LED connection cable.
LED Connection Cable
2. Remove the ARM module.

6.6.2 Removing the Backlight Board

To remove the backlight board:
1. Remove the backlight cable and four M3x6 screws to remove the backlight board..
Backlight Board Cable
6.6.3 Removing the LED Display Assembly

To remove the LED display assembly:
1. Remove the six M3x8 screws.
LED Connection
Cable
Backlight Board
Cable
2. Remove the LCD Display with metal fixing plate gently and remove the ARM cable and the backlight
board cable.

3. Remove the four M2.5x6 screws and remove the LCD Display and LCD Display Connection cable.
6.6.4 Removing the Alarm LED Board

To remove the Alarm LED board:
1. Remove the alarm LED cable.
2. Remove the two M3x8 self-tapping screws.
3. Remove the alarm LED board.

6.6.5 Removing the Keypad Board

To remove the keypad board:
1. Remove the code cable and the alarm LED cable.
Code Cable Alarm LED cable
2. Remove the six M3x8 self-tapping screws.
3. Remove the keypad board.
6.6.6 Removing the Code Board

To remove the code board:
1. Unplug the navigation wheel cap.
Pull Upright
2. Use Hexagon nut driver to remove the nut.

3. Remove the code board.
6.7 Disassembling the Rear Case

The rear case assembly includes following main components:
• Main frame assembly:
– Connector panel
– SpO2 module
– IBP/TEMP module
– ECG module
– CO2 module
– NIBP module
– System board
– AC/DC power module
– Battery board
– AC power connector assembly
– I/O module
• Rear frame assembly:
– Fan
– Speaker
6.7.1 Removing the Main Frame From the Rear Frame

To remove the main frame from the rear frame:
1. Remove the five M3x6 screws and remove speaker and fan cables.
Speaker Cable
Fan Cable

2. Turn the monitor over and remove three M4x6 screws.
3. Press the connector panel and gently pull out the main frame from the rear frame.

6.7.2 Removing the Connector Panel

To remove the connector panel:
1. Remove the IBP/TEMP connector cable and SpO2 connector cable.
SpO2 Connector Cable
IBP Connector Cable
TEMP Connector Cable
2. Remove ECG cable and NIBP tube.
ECG Cable
NIBP Tube
3. Remove CO2 tube and socket.

4. Remove the connector panel.
5. Remove the four M3x8 self-tapping screws and remove the TEMP connetor assembly.
TEMP Connector Assembly
6. Remove the Fixing Auxiliary board and temputer Procetive sockets. Then remove the TEMP connector.
Fixing Auxiliary Board
Procetvie Socket
7. Remove the eight M3x8 self-tapping screws and remove the IBP connetor.

8. Remove the four M3x8 self-tapping screws and remove the ECG connetor.
9. Remove the threefour M3x8 self-tapping screws and remove the SpO2 connetor.
To install the CO2 socket:

1. Install the tube to the outlet.
2. Install the fixed socket.

3. Set the socket into the connector panel, and rotate it anticlockwise.
4. Install the screws.
6.7.3 Removing the SpO2 Module

To remove the SpO2 module:
1. Remove the two M3X6 screws.
2. Remove the SpO2 module gently.

6.7.4 To remove the IBP/TEMP Module

To remove the IBP/TEMP module:
2. Remove the IBP/TEMP module gently.
6.7.5 Removing the ECG Module

To remove the ECG module:
1. Remove the three M3X6 screws.
2. Remove the ECG module gently.

6.7.6 To remove the CO2 module

To remove the CO2 module:
1. Remove CO2 cable and the four M3X6 screws.
CO2 Cable
2. Remove the CO2 module gently.
6.7.7 Removing the NIBP Module

1. Remove the NIBP cable and the four M3X6 screws.
NIBP Cable

2. Remove the NIBP module gently.
6.7.8 Removing the Main Board Module

1. Remove the eight M3x6 screws.
2. Remove the Main Board gently.

6.7.9 Removing the AC/DC Power Module

2. Remove the power module gently.
6.7.10 Removing the Battery Board

2. Remove the battery board gently.

6.7.11 Removing the AC Power Connector Assembly

2. Use the long flat nose plier or spanner to remove the nut.
Nut
3. Remove the AC power connector assembly gently.

6.7.12 Removing the I/O Module

1. Remove the three M3x4 screws.Remove the I/O module gently.
2. Remove the CRT cable and two M3x6 screws.
CRT Cable
3. Remove the I/O board.
4. Use the Hexagon Nut driver to remove the two nuts.

Rear Frame disassembly
5. Remove the CRT socket.
6.8 Rear Frame disassembly
6.8.1 Removing the Fan and the Speaker Assembly

1. Remove the white-clip M3X6 screw and four screws.
2. Remove the fan and the speaker.

6.8.2 Removing the Handle Assembly

To remove the handle assembly:
2. Remove the handle fixing frame.
Handle Fixing Frame
3. Pull out the handle assembly.
4. Remove the four M3x8 screws and washes.

5. Separate the front and back carry handle.
Front Carry Handle Back Carry Handle


7
Assembly Diagrams and Spare Parts
This Chapter describes the assembly diagrams and the parts that are replaceable on G30/G40 Patient
Monitor.
7.1 G40 Main Assembly Exploded Diagram
Figure 7-1 G40 Main Assembly Exploded Diagram

G40 Front Case Assembly and Parts
Item Description P/N

1 Front Case NA
2 Main Frame NA
3 G-3G4G Function Panel Standard (Connector Panel) 453564312881
G-3G4G Function Panel W/ SPO2 IBP (standard + IBP) 453564312891
G-3G4G Function Panel W/ SPO2 CO2 (standard + CO2) 453564312901
G-3G4G Function Panel W/ SPO2 IBP CO2 (standard + IBP + CO2) 453564312911
G-4G Function Panel W/ SPO2 IBP CO2 C.O. (standard + IBP + 453564312921
CO2 + C.O.)
4 Rear FrameAssembly NA
5 GR Thermal Recorder, Ver B 453564287591
Table 7-1 G40 Main Assembly Part List
7.2 G40 Front Case Assembly and Parts
Figure 7-2 G40 Front Case Assembly Exploded Diagram-1

9
7
Figure 7-3 G40 Front Case Assembly Exploded Diagram-2

1 Inverter TPI-02-0426-K 12V(G40) 453564297351
2 ARM Module 2 (G30/G40) 453564324091
3 Front Case and Display Assembly (G40) N/A
4 DSPL 12.1'' LCD Display, AU, G121SN01 V3 (Display 453564290941

Assembly G40)
5 G-4G Front Panel ASSY White 453564439891
6 G-6G PLAST Navigation Wheel 453564297341
7 PCA Alarm LED Board C-ALARM012A 453564312681
8 PCA Code Board C-CODE011D 453564297371
9 PCA Key Board M-7C1K11C Pb free (G40) 453564341811
Table 7-2 G40 Front Case Assembly Parts List

G40 Rear Frame Assembly and Parts
7.3 G40 Rear Frame Assembly and Parts
Figure 7-4 G40 Rear Frame Assembly Exploded Diagram

1 G-3G4G Speaker ASSY 453564312821
2 UT-4B CBL Main Unit Fan Connection (Fan ASSY) 453564339711
3 G-4G Rear Case ASSY White 453564439901
Table 7-3 G40 Rear Frame Assembly Parts List

G40 Main Frame Assembly and Parts
7.4 G40 Main Frame Assembly and Parts
Figure 7-5 G40 Main Frame Assembly Exploded Diagram-1

1 SS PCA SpO2 For Service 453564403911


2 PCA TEMP Module C-IBPTEMPCO013A 453564312731
(IBP/TEMP Module)
PCA IBP/TEMP Module C-IBPTEMPCO013A 453564290881
PCA Isolated IBPTEMPCO C-IBPTEMPCO013A 453564289421

(G40)
C.O. Module Assembly G40COL01A 453564290151
3 PCA SYS Board (Main Board Assembly G30/G40) 453564356621
Table 7-4 G40 Main Frame Assembly Parts-1
Figure 7-6 G40 Main Frame Assembly Exploded Diagram-2

1 PCA AC PWR Interface BD, C-G40F011A V1.0 453564312751
(AC Power Assembly G40)
2 PCA ECG Module C-ECG7131C V1.2 453564304531

(ECG Module)


3 PCA NIBP Module Assembly C-NIBP312B 453564288791
(NIBP Module)
4 PCA ORI-CO2 MDL, MINIMEDICO2-9, RS-08630 453564312671

(CO2 Module)
5 PCA External Output Board M-4B2C02B 453564312711

(I/O Module Assembly G30/G40)
Table 7-6 G40 Main Frame Assembly Exploded Diagram-3
Item Description Philips P/N

1 ASSY-PWR SMPS LPS54-M 15V 60W ASTEC 453564288691
(AC/DC Power Module)
2 G-4G Batteries Connect ASSY 453564312791

(Battery Board G40)
3 Lead-acid Battery 989803166441

G30 Main Assembly Exploded Diagram
7.5 G30 Main Assembly Exploded Diagram
3
1 2
4
Figure 7-7 G30 Main Assembly Exploded Diagram

1 Front Case NA
2 Main Frame NA
3 G-3G4G Function Panel Standard (Connector Panel) 453564312881
G-3G4G Function Panel W/ SPO2 IBP (standard + IBP) 453564312891
G-3G4G Function Panel W/ SPO2 CO2 (standard + CO2) 453564312901
G-3G4G Function Panel W/ SPO2 IBP CO2 (standard + IBP + CO2) 453564312911
4 Rear Frame NA
5 GR Thermal Recorder, Ver B 453564287591
Table 7-8 G30 Main Assembly Exploded Diagram List

7.6 G30 Front Case Assembly and Parts
7
9
Figure 7-8 G30 Front Case Assembly Exploded Diagram

1 G-3G Front Panel ASSY (G30) White 453564439911
2 ARM Module 1 (G30 only) 453564369871
ARM Module 2 (G30/G40) 453564324091
3 PCA G40TSLP01A V1.0 W/O TS Pb Free (Backlight 453564425671

Board)
4 DSPL 10.4'' LCD Display, AU, G104SN03 V1 453564400761

(Display Assembly G30)
5 PCA Key Board M-G301K01A Pb free (G30) 453564341911
6 G-3G PLAST Silicon Keys, PHILIPS 453564353711
Table 7-9 G30 Front Case Assembly Parts List

G30 Rear Frame Assembly and Parts
7.7 G30 Rear Frame Assembly and Parts
1
2
Figure 7-9 G30 Rear Case Assembly Exploded Diagram

1 G-3G4G Speaker ASSY 453564312821
2 UT-4B CBL Main Unit Fan Connection (Fan ASSY) 453564339711
3 G-3G Rear Case ASSY White (G30) 453564439921
Table 7-10 G30 Rear Case Assembly Parts List

7.8 G30 Main Frame Assembly and Parts
3 13
12
11 10
6
7 8 9
Table 7-11 G30 Main Frame Assembly Exploded Diagram

2 PCA IBP/TEMP Module C-IBPTEMPCO013A 453564290881

(IBP/TEMP Module)
PCA TEMP Module C-IBPTEMPCO013A 453564312731

5 G-3G Battery Connect ASSY (Battery Board G30) 453564312811
6 G-3G PCA AC Power CONN Board Ver1.1 453564312741

(AC power assembly G30)
7 SLC-YD MACH PWR Cord Lock Catch, SUS304 453564297361
8 PCA ORI-CO2 MDL, MINIMEDICO2-9, RS-08630 (CO2 453564312671

Module)
9 PCA NIBP Module Assembly C-NIBP312B (NIBP Module) 453564288791

Spare Parts List

10 PCA ECG Module C-ECG7131C V1.2 (ECG Module) 453564304531
11 G-4G PLAST External Output Panel Film 453564325191

Table 7-12 G30 Main Frame Assembly Parts List
7.9 Spare Parts List

G30
Item Descriptions P/N

1 PCA Main Board C-ARM211B V1.1 Pb Free (ARM Module 1) 453564369871
2 PCA Main Board C-ARM211B V1.1 (ARM Module 2) 453564324091
3 PCA G40TSLP01A V1.0 W/O TS Pb Free (Backlight Board) 453564425671
4 DSPL 10.4'' G104SN03 V5 TFT LVDS LED AU(LCD 453564400761

Display)
5 XFMR Inverter TPI-01-0110 12V 453564311421
6 DSPL 10.4'' LCD Display, AU, G104SN03 V1 (Display 453564290871

Assembly G30)
10 PCA Key Board M-G301K01A Pb free (G30) 453564341911
12 G-3G CBL LED Display Connection (LED Connection Cable) 453564416611
13 G-3G CBL 10'' LED Screen Backlight (Backlight Board Cable) 453564409511
14 UT-4B CBL Alarm LED Connection (Alarm Cable) 453564311541
15 UT-4B CBL Encode Connection (Code Cable) 453564311521
16 G-3G Front Panel ASSY (G30) Blue 453564312841
17 G-3G Front Panel ASSY (G30) White 453564439911

(IBP/TEMP Module)

Spare Parts List


(ECG Module)

(NIBP Module)

Module)
26 G-3G PCA AC Power CONN Board Ver1.1 453564312741


28 G-3G Battery Connect ASSY (Battery Board G30) 453564312811
30 G-4G CBL ECG Board Connection ( ECG -- System board) 453564326311
31 CBL Oridion-CO2 Socket Connection (CO2 -- System board) 453564311681
32 CBL 1x7PIN, 2.54, 55mm (NIBP---System board) 453564312531
33 CBL 1x8PIN, 2.54, 140mm (Recorder---System board) 453564311701
34 UT-4B CBL Inverter Power (Backlight board --- System board) 453564311491
35 CBL 2x8PIN, 2.0, 120mm (Keypad board -- System board) 453564311721
36 CBL 2x15PIN, 2.0, 180mm (ARM board -- System board) 453564311711
37 CBL 2x17PIN, 2.0, 180mm (ARM board -- I/O board) 453564312591
38 UT-7C CBL CRT Connection (CRT cable) 453564311551
39 CBL LCD Display Grounding 453564311961
40 G-4G CBL TEMP Socket Connection 453564340041
41 G-4G CBL ECG Socket Connection 453564340081
42 CBL Picosat-SPO2 Socket Connection 453564312581
43 G-4G CBL Dual-IBP Socket Connection 453564311691
44 G Function Panel Standard 3G/4G 453564312881
45 G Function Panel W/ SPO2 IBP 3G/4G 453564312891
46 G Function Panel W/ SPO2 CO2 3G/4G 453564312901
47 G Function Panel W/ SPO2 IBP CO2 3G/4G 453564312911
48 Main Unit Fan 12V 60*60*20 453564339711
49 G Speaker ASSY 3G/4G 453564312821
51 G-3G Rear Case ASSY(Blue) 453564312861

Spare Parts List

52 Thermal Recorder Ver.B GR50 453564287591
53 G-3G PLAST Function Panel Film, Standard 453564325211
54 G-4G PLAST FCTN Panel Film, STD/IBP 453564390491
55 G-4G PLAST Function Panel Film, STD/CO2 453564353101
56 G-4G PLAST FCTN PNL Film, STD/CO2/IBP 453564353091
58 CONN Quick NIBP Socket, with Nut 453564311991
60 G-3G PLAST Front Carry Handle, PHILIPS (White) 453564353681
61 G-3G PLAST Front Carry Handle, PHILIPS (White) 453564353691
62 G-3G PLAST Ver B Back Carry Handle (Blue) 453564353491
63 G-3G PLAST Ver B Front Carry Handle (Blue) 453564390471
G40:

1 PCA Main Board C-ARM211B V1.1 (ARM Module 2) 453564324091
2 XFMR Inverter TPI-02-0426-K 12V 453564297351
3 DSPL 12.1'' LCD Display, AU, G121SN01 V3 453564290941
7 PCA Key Board M-7C1K11C Pb Free 453564341881
9 G-4G CBL LCD Connection, STM Housing 453564311771
10 UT-4B CBL Alarm LED Connection (Alarm Cable) 453564311541
11 UT-4B CBL Encode Connection (Code Cable) 453564311521
12 G-4G Front Panel ASSY 453564312831
13 G-4G Front Panel ASSY White 453564439891

(IBP/TEMP Module)
17 PCA Isolated IBPTEMPCO C-IBPTEMPCO013A 453564289421

Spare Parts List

18 C.O. Module Assembly G40COL01A 453564290151


(ECG Module)

(NIBP Module)

Module)
24 PCA AC PWR BD, C-G40F011A V1.0 Pb Free 453564312751


26 G-4G Batteries Connect ASSY (Battery Board G40) 453564312791
28 G-4G CBL ECG Board Connection ( ECG -- System board) 453564326311
29 CBL Oridion-CO2 Socket Connection (CO2 -- System board) 453564311681
30 CBL 1x7PIN, 2.54, 55mm (NIBP---System board) 453564312531
31 CBL 1x8PIN, 2.54, 140mm (Recorder---System board) 453564311701
32 CBL 1x6PIN, 1.25, 310mm (Inverter --- System board) 453564312511
33 CBL 2x8PIN, 2.0, 120mm (Keypad board -- System board) 453564311721
34 CBL 2x15PIN, 2.0, 180mm (ARM board -- System board) 453564311711
35 CBL 2x17PIN, 2.0, 180mm (ARM board -- I/O board) 453564312591
36 UT-7C CBL CRT Connection (CRT cable) 453564311551
37 CBL LCD Display Grounding 453564311961
38 G-4G CBL TEMP Socket Connection 453564340041
39 G-4G CBL ECG Socket Connection 453564340081
40 CBL Picosat-SPO2 Socket Connection 453564312581
41 G-4G CBL Dual-IBP Socket Connection 453564311691
42 G Function Panel Standard 3G/4G 453564312881
43 G Function Panel W/ SPO2 IBP 3G/4G 453564312891
44 G Function Panel W/ SPO2 CO2 3G/4G 453564312901
45 G Function Panel W/ SPO2 IBP CO2 3G/4G 453564312911
46 G-4G Function Panel W/ SPO2 IBP CO2 C.O. 453564312921
47 Main Unit Fan 12V 60*60*20 453564339711

Spare Parts List

48 G-4G PLAST Front Carry Handle, PHILIPS White 453564325151
49 G-4G PLAST Front Carry Handle, PHILIPS White 453564325131
50 G-4G PLAST Carry Handle Left Pothook White 453564325171
51 G-4G PLAST Carry Handle Right Pothook White 453564325181
52 G-4G PLAST Ver B Front Carry Handle Blue 453564353431
53 G-4G PLAST Ver B Back Carry Handle Blue 453564353421
54 G-4G PLAST Carry Handle Left Pothook Blue 453564353441
55 G-4G PLAST Carry Handle Right Pothook Blue 453564353451
56 G Speaker ASSY 3G/4G 453564312821
58 G-4G Rear Case ASSY Blue 453564312851
59 Thermal Recorder Ver.B GR50 453564287591
60 G-3G PLAST Function Panel Film, Standard 453564325211
61 G-4G PLAST FCTN Panel Film, STD/IBP 453564390491
62 G-4G PLAST Function Panel Film, STD/CO2 453564353101
63 G-4G PLAST FCTN PNL Film, STD/CO2/IBP 453564353091
64 G-4G PLAST FCTN Panel Film STD+IBP+C.O. 453564398981
66 G-4G PLAST Function Panel Film 453564398991
67 CONN Quick NIBP Socket, with Nut 453564311991

8
Electromagnetic Compatibility
This chapter lists the tests and compliance levels that make the G30/G40 patient monitor suitable for use in
the specified electromagnetic environment according to IEC 60601-1-2:2000/A1:2007.
8.1 Instructions for Use

Medical electrical equipment can either generate or receive electromagnetic interference. This product has
been evaluated for electromagnetic compatibility (EMC) with the appropriate accessories according to
IEC60601-1-2:2007, the international standard for EMC for medical electrical equipment. This IEC
standard has been adopted in the European Union as the European Norm, EN 60601-1-2:2007. Radio
frequency (RF) interference from nearby transmitting devices can degrade performance of the product.
Electromagnetic compatibility with surrounding devices should be assessed prior to using the product.
Fixed, portable, and mobile radio frequency communications equipment can also affect the performance of
medical equipment. See your service provider for assistance with the minimum recommended separation
distance between RF communications equipment and the product.
The cables, sensors/transducers, and other accessories for which compliance is claimed are listed in this
service guide.
Warning Use of accessories, transducers, and cables other than those specified may result in increased emissions
and/or decreased immunity of the G30/G40 patient monitor.
G30/G40 patient monitor should not be used adjacent to or stacked with other equipment. If adjacent
or stacked use is necessary, the monitor should be observed to verify normal operation in the
configuration in which it is used.
Caution The following ports on G30/G40 patient monitor are sensitive to electrostatic discharge during patient
monitoring:
• SpO2
• ECG
Follow these guidelines to reduce electrostatic discharge:
• Do not touch the connector pins of the port.
• When connecting and disconnecting cables to the ports, use ESD precautionary measures.
Precautionary measures may include the following:
– Make sure you are grounded prior to connection or touch grounded metal.
– Wear an ESD grounding strap and an ESD protective garment.
– Provide ESD training to all users. Users should understand what electrostatic discharge is, how
damage can occur, and how to prevent ESD.
8.2 Guidance and Manufacturer's EMC Declaration

The G30/G40 patient monitor is intended for use in the electromagnetic environment specified in the
following tables. The customer or the user of the G30/G40 patient monitor should assure that it is used in
such an environment.

Guidance and Manufacturer's EMC Declaration
8.2.1 Electromagnetic Emissions for all Equipment and Systems
Table 8-1 Electromagnetic Emissions for all Equipment and Systems
Emission test Compliance Electromagnetic Environment Guidance
RF emissions Group 1 The G30/G40 patient monitor uses RF energy only for its internal
function. Therefore, its RF emissions are very low and are not
CISPR 11
likely to cause any interference in nearby electronic equipment.
RF emission Class A
CISPR 11 The G30/G40 patient monitor is suitable for use in all
establishments, other than domestic establishments and those
Harmonic emissions Class A directly connected to the public low-voltage power supply network
IEC 61000-3-2 that supplies buildings used for domestic purposes.
Voltage fluctuations/ Complies

flicker emissions
IEC 61000-3-3
8.2.2 Electromagnetic Immunity for all Equipment and Systems
Table 8-2 Electromagnetic Immunity for all Equipment and Systems
Electromagnetic Environment
Immunity Test IEC 60601 Test Level Compliance Level
– Guidance
Electrostatic ±6 kV contact ±6 kV contact Floors should be wood, concrete or

discharge (ESD) ceramic tile. If floor are covered
±8 kV air ±8 kV air
with synthetic material, the relative
IEC 61000-4-2
humidity should be at least 30%.
Electrical fast ±2 kV for power supply ±1 kV for power supply Mains power quality should be that
transient/burst lines lines of a typical commercial or hospital
environment. It recommends the use
IEC 61000-4-4
of filters on power input lines.
Surge ±1 kV differential mode ±1 kV differential mode Mains power quality should be that
of a typical commercial or hospital
IEC 61000-4-5 ±2 kV common mode ±2 kV common mode
environment.

Table 8-2 Electromagnetic Immunity for all Equipment and Systems (Continued)
Electromagnetic Environment
Immunity Test IEC 60601 Test Level Compliance Level
– Guidance
Voltage dips, short <5% UT1 <5% UT Mains power quality should be that
interruptions and (>95% dip in UT) (>95% dip in UT) of a typical commercial or hospital
voltage variations on for 0.5 cycle for 0.5 cycle environment. If the user of the G30/
power supply input G40 Patient Monitor requires
lines continued operation during power
40% UT
40% UT mains interruptions. It is
IEC 61000-4-11 (60% dip in UT) (60% dip in UT) recommended that the G30/G40
for 5 cycles for 5 cycles Patient Monitor be powered from an
uninterruptible power supply or a
70% UT battery.
70% UT
(30% dip in UT)
(30% dip in UT)
for 25 cycles
for 25 cycles
<5% UT
<5% UT
(>95% dip in UT)
(>95% dip in UT)
for 5 sec
for 5 sec
Power frequency (50/ 3A/m 3A/m Power frequency magnetic fields

60Hz) magnetic field Should be at levels characteristic of
a typical location in a typical
IEC61000-4-8
commercial or hospital
environment.
1. UT is the AC mains voltage prior to application of the test level.

8.2.3 Electromagnetic Immunity for Equipment and Systems not Life-Supporting

Table 8-3 Electromagnetic Immunity for Equipment and Systems not Life-Supporting
IEC60601 Test Compliance

Immunity Test Electromagnetic Environment – Guidance
Level Level
Portable and mobile RF communications equipment

should be used no closer to any part of the G30/G40
Patient Monitor, including cables, than the recommended
separation distance calculated from the equation
applicable to the frequency of the transmitter.
Recommended separation distance

Conducted RF 3 Vrms 3 Vrms
 3 .5 
IEC 61000-4-6 150 kHz to 80 MHz d =  P
 V1 
Radiated RF 3 V/m 3 V/m

IEC 61000-4-3 80 MHz to 2.5 GHz
 3.5 
d =  P
 V1 
7
d = ----- P
E1
Where P is the maximum output power rating of the
transmitter in watts (W) according to the transmitter
manufacturer and d is the recommended separation
distance in meters (m).
Field strengths from fixed RF transmitters, as determined
by an electromagnetic site survey,1 should be less than
the compliance level in each frequency range.2
Interference may occur in the vicinity of equipment
marked with the following symbol:
1. Field strengths from fixed transmitters, such as base stations for radio (cellular/cordless) telephones and land mobile
radios, amateur radio, AM and FM radio broadcast and TV broadcast cannot be predicted theoretically with accuracy.
To assess the electromagnetic environment due to fixed RF transmitters, an electromagnetic site survey should be con-
sidered. If the measured field strength in the location in which the G30/G40 patient monitor is used exceeds the appli-
cable RF compliance level above, the G30/G40 patient monitor should be observed to verify normal operation. If
abnormal performance is observed, additional measures may be necessary, such as reorienting or relocating the G30/
G40 patient monitor.
2. Over the frequency range 150 kHz to 80 MHz, field strengths should be less than 3 V/m.

8.2.4 Recommended Separation Distances

The G30/G40 patient monitor is intended for use in an electromagnetic environment in which radiated RF
disturbances are controlled. The customer or the user of the G30/G40 patient monitor can help prevent
electromagnetic interference by maintaining a minimum distance between portable and mobile RF
communications equipment (transmitters) and the G30/G40 patient monitor as recommended below, according
to the maximum output power of the communications equipment.
Table 8-4 Recommended Separation Distances Between Portable and Mobile RF Communications
Equipment and G30/G40 patient monitor
Separation Distance According to Frequency of Transmitter (m) 1
Rated Maximum Output 150 kHz to 80 MHz 80 MHz to 800 MHz 800 MHz to 2.5 GHz
Power Of Transmitter
(W) 3.5 3.5 7
d = ------- P d = ------- P d = ----- P
V1 E1 E1
0.01 0.12 0.12 0.23
0.1 0.37 0.37 0.74
1 1.17 1.17 2.33
10 3.69 3.69 7.38
100 11.67 11.67 23.33
1. For transmitters rated at a maximum output power not listed above, the recommended separation distance (d) in
metres (m) can be estimated using the equation applicable to the frequency of the transmitter, where P is the maxi-
mum output power rating of the transmitter in watts (W) according to the transmitter manufacturer.
Note — At 80 MHz and 800 MHz, the separation distance for the higher frequency range applies. These
guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection
from structures, objects and people.
8.2.5 Interference Test Results

The following interference test results do not affect patient diagnoses.
Table 8-5 Interference Results
Immunity Test IEC 60601 Test Level Compliance Level Results
Electrical fast ±2 kV for power supply lines 1 kV for power supply Adding ±2 kV interference to the
transient/burst lines power supply line heavily interfered
with the ECG waveform.
IEC 61000-4-4
Decreasing interference to ±1 kV
slightly interfered with the
waveform. Removing the
interference returned the waveform
to the previous operating mode
within 10 seconds with no loss of
stored data.


Index
C front case, 5-2, 5-3
alarm LED board, 5-7
configuration
arm module, 5-5
system, 3-1
code board, 5-8
inverter, 5-6
D keypad board, 5-8
demo mode LCD display, 5-6
set, 1-7 installing CO2 socket, 5-14
rear case
E , 5-9
AC power connector, 5-18
EMC
battery board, 5-17
electromagnetic emissions
CO2 module, 5-13
all, 8-2
ECG module, 5-12
electromagnetic immunity
fan and speaker, 5-20
all, 8-2
I/O module, 5-19
not life-supporting, 8-4
IBP and C.O., 5-10
instructions for use, 8-1
main borad module, 5-16
interference test, 8-5
main frame, 5-11
separation distances, 8-5
NIBP module, 5-15
exploded diagram
SpO2 module, 5-9
G30, 7-8
recorder, 5-2
G40, 7-1
tools, 5-1
exploded diagram, G30
G40, disassembly
front case, 7-9 fuse, 5-2
main frame, 7-11
G40,disassembling
rear frame, 7-10
rear case
exploded diagram, G40 AC/DC power module, 5-16
front case, 7-2
main frame, 7-5
rear frame, 7-4 N
network
G configure the connection, 1-7
disconnect, 1-7
G30, disassembling enable, 1-7
bettery, 6-1
front case, 6-3
alarm LED board, 6-7 P
backlight board, 6-6 parts
code board, 6-8 all, 7-12
keypad board, 6-8 parts, G30
LCD display, 6-6 front case, 7-9
fuse, 6-2 main frame, 7-11
installing CO2 socket, 6-13 rear frame, 7-10
rear case parts, G40
AC power connector, 6-19 front case, 7-2
AC/DC power module, 6-18 main frame, 7-5
battery board, 6-18 rear frame, 7-4
CO2, 6-16 product
connector panel, 6-11 configurations, 1-4
ECG module, 6-15 installing requirment, 1-5
fan and speaker, 6-21 main components, 1-3
I/O module, 6-20 networking capabilities, 1-4
IBP and TEMP module, 6-15 overview, 1-3
main board module, 6-17 repair strategy, 1-1
main frame, 6-9 replaceable parts, 1-1
NIBP module, 6-16 service, i-6
SpO2 module, 6-14 unpack, 1-5
recorder, 6-2 warranty information, i-5
tools, 6-1 product information
G40, disassembling manufacturer, i-2
battery, 5-1 manufacturer’s responsibility, 2-1
G30/G40 Patient Monitors Service Guide Index-1

standard, i-2 ECG processing, 3-4
etCO2, 3-5
R I/O module, 3-3
IBP processing, 3-4
regulatory and safety specifications, i-2 keys and navigation wheel, 3-3
requirements
NIBP processing, 3-3
enviromental, 1-2
nurse call contacts, 3-6
space, 1-2
power management, 3-6
RJ45 port, 1-4
recorder, 3-3
speaker, 3-3
S SpO2 processing, 3-4
safety specification, i-2 system module, 3-2
Safety Standards, i-5 temperature processing, 3-5
software troubleshooting
upgrade, 1-9 alarm, 4-4
specifications C.O., 4-6
power, 1-3 display, 4-3
standard ECG/Respiration, 4-7
safety, i-5 etCO2, 4-6
Symbols, i-3 NIBP, 4-4
symbols performance verification tests, 4-8
on monitor and packaging, i-3 power, 4-1
symbols, on monitor and packaging, i-3 recorder, 4-7
SpO2, 4-6
T temperature, 4-5
test
electrical safety, 2-10
ibp test cable, 2-3
recorder, 2-13
recording, 2-4
temp test cable, 2-3
test equipments, 2-2
test frequency, 2-2
test guidelines, 2-1
test, calibration
CO2, 2-9
IBP, 2-10
NIBP, 2-9
test, performance
C.O., 2-7
display, 2-5
ECG, 2-6
IBP, 2-6
network, 2-10
NIBP, 2-8
overpressure, 2-9
pluse SpO2, 2-7
power supply, 2-5
respiration, 2-6
speaker, 2-5
temperature, 2-6
visual, 2-5
test, safety
patient leakage current with mains voltage, 2-12
protective earth continuity, 2-12
system enclosure leakage, 2-11
testing
performance verification tests
IBP calibration, 2-10
theory
AC/DC power module, 3-3
arm module, 3-2
C.O., 3-5
Index-2 G30/G40 Patient Monitors Service Guide

Printed in China
Third Edition
453564308371 453564308371
3.0 3.0

G30-G40 Servicio ENG

Uploaded by

Copyright:

Available Formats

G30-G40 Servicio ENG

Uploaded by

Document Information

Copyright

Available Formats

Share this document

Share or Embed Document

Sharing Options

Did you find this document useful?

Is this content inappropriate?

Copyright:

Available Formats

G30-G40 Servicio ENG

Uploaded by

Copyright:

Available Formats

G30/G40

No. 2 Tiangong Road, Nanshan District, Shenzhen, P. R. China 518057

Tel: +86 755 26980999

Shenzhen Goldway Industrial Inc.

Regulatory and Safety Specifications

2 G30/40 Patient Monitors Service Guide

Table 1 Monitor and Packaging Symbols

Symbol Description Symbol Description

CE mark Fragile, handle with care

Recyclable Keep upright

Recovery Maximum stacking

Humidity limitation Caution, consult accompanying

BF applied part: including F CF applied part: including F

Temperature limitation Atmospheric limitation

Keep dry Param Menu key

On/Standby key Waveform Freeze key

Main Menu key Alarm silence key

Print key NIBP key

SpO2 probe connector C.O. connector

ECG connector CO2 connector

G30/40 Patient Monitors Service Guide 3

Symbol Description Symbol Description

IBP1 connector IBP2 connector

NIBP cuff connector TEMP1 connector

TEMP2 connector Gas input

AC Power LED Charging LED

Date of manufacture Manufacturer address

Equipotential grounding post Dangerous voltage

EU representatives Display output

Nurse call connector ECG analog output port

Consult Instructions for use Serial Number

Protective grade USB port

Gas output Fuse

Protective grounding Ethernet port

4 G30/40 Patient Monitors Service Guide

Table 2 Safety Standards

Degree of Protection Type CF defibrillator-proof: per IEC 60601-1

Sterilization and disinfection As recommended by manufacturer

Mode of Operation Continuous

Product Support and Warranty Information

Keep the packing case for transport, storage, or maintenance.

• product is assembled, upgraded, altered, or maintained by authorized service representatives.

• damage is caused by the following:

G30/40 Patient Monitors Service Guide 5

1. Contact your local Goldway representative.

2. For further support, contact Goldway Customer Service Department.

Customer Service Department of Shenzhen Goldway Industrial Inc.

International call center hours:

Monday – Friday (except Chinese statutory holidays)

Tel: +86 755 86278308

Service and support are available in Chinese and English only.

Before calling for service, note the following information:

• Model and serial number of the monitor

Note — A Note calls attention to an important point in the text.

6 G30/40 Patient Monitors Service Guide

Only use the monitor on one patient at a time.

Never use the monitor to monitor apnea.

The monitor is not for home use.

The monitor is not for diagnostic or therapeutic use.

Never use the monitor during MRIs or CT scans.