GE Logiq P5 Service Manual

							GE HEALTHCARE
DIRECTION 5394141, REVISION 1LOGIQ™ P5 SEVICE MANUAL
Section 1-3 - Safety Considerations 1-13
1-3-3 Mechanical Safety (cont’d)
NOTE: Special care should be taken when transporting the unit in a vehicle: • Secure the unit in an upright position.
• Lock the wheels (brake)
• DO NOT use the Control Panel as an anchor point.
• Place the probes in their carrying case.
• Eject DVD media from the system.
1-3-4 Electrical Safety
To minimize shock hazard, the eq uipment chassis must be connecte d to an electrical ground. The 
system is equipped with a three-conductor AC power  cable. This must be plugged into an approved 
electrical outlet with safety ground . If an extension cord is used with t he system, make sure that the total 
current rating of the system does not exceed the extension cord rating. 
The power outlet used for this equipment should  not be shared with other types of equipment.
Both the system power cable and the power connec tor meet international electrical standards.
CAUTIONKeep the heat venting holes on the monitor unobstructed to avoid overheating of the 
monitor.
WARNINGWARNINGDO NOT SERVICE OR DISASSEMBLE PARTS UNDER FRU UNIT LEVEL AT ANY 
CIRCUMSTANCES. 
						

							GE HEALTHCARE
DIRECTION 5394141, REVISION 1LOGIQ™ P5 SEVICE MANUAL 
1-14 Section 1-3 - Safety Considerations
1-3-5 Label Locations
1.) Identification and Rating Plate - USA/Asia 120V Console
2.) Identification and Rating Plate - Europe/Asia/Latin America 220V Console
3.) Identification and Rating  Plate - Japan 100V Console
4.) Identification and Rating  Plate - Korea 220V Console
5.) Identification and Rating Plate - China 220V Console
6.) UL Label Figure 1-1   OUTSIDE MARKINGS OF LOGIQ™ P5 (Rear) 
						

							GE HEALTHCARE
DIRECTION 5394141, REVISION 1LOGIQ™ P5 SEVICE MANUAL
Section 1-3 - Safety Considerations 1-15
1-3-5 Label Locations (cont’d)
1.) Possible Shock Hazard
2.) Label -”Do not use the following devices near this equipment.” 
3.) Label - “The equipment weighs approximately 75kg.
4.) Prescription Devices
5.) CE Mark Label (Left), WEEE Label (Right)
6.) CISPR Label
7.) Grounding reliability Label
8.) Voltage Range Indication and Power indication Label
9.) Standard LCD Arm & flexible LCD Arm Option Label & Mercury Label
10.) LCD Arm Rotation Label Figure 1-2   OUTSIDE MARKINGS OF LOGIQ™ P5 
						

							GE HEALTHCARE
DIRECTION 5394141, REVISION 1LOGIQ™ P5 SEVICE MANUAL 
1-16 Section 1-3 - Safety Considerations
1-3-6 Dangerous Procedure Warnings
Warnings, such as the examples below, precede pot entially dangerous procedures throughout this 
manual. Instructions contained in the warnings must be followed.
1-3-7 Lockout/Tagout Requir ements (For USA Only)
Follow OSHA Lockout/Tagout requirements by ensuring  you are in total control of the electrical Mains 
plug.
DANGERDANGEROUS VOLTAGES,  CAPABLE OF CAUSING DEATH, ARE PRESENT 
IN THIS EQUIPMENT. USE EXTREME  CAUTION WHEN HANDLING, TESTING 
AND ADJUSTING.
WARNINGWARNINGEXPLOSION WARNING
DO NOT OPERATE THE EQUIPMENT IN AN EXPLOSIVE ATMOSPHERE. 
OPERATION OF ANY ELECTRICAL EQ UIPMENT IN SUCH AN ENVIRONMENT 
CONSTITUTES A DEFINITE SAFETY HAZARD.
WARNINGWARNINGDO NOT SUBSTITUTE PART S OR MODIFY EQUIPMENT
BECAUSE OF THE DANGER OF INTRODUCING ADDITIONAL HAZARDS, DO NOT 
INSTALL SUBSTITUTE PARTS OR PERFORM ANY UNAUTHORIZED MODIFICATION 
OF THE EQUIPMENT. 
						

							GE HEALTHCARE
DIRECTION 5394141, REVISION 1LOGIQ™ P5 SEVICE MANUAL
Section 1-4 - EMC, EMI, and ESD 1-17
Section 1-4
EMC, EMI, and ESD
1-4-1 Electromagnetic Compatibility (EMC)
Electromagnetic compatibility describes a level of performance of a device within its electromagnetic 
environment. This environment consists of the device itself and its surroundings including other 
equipment, power sources and persons with which the device must  interface. Inadequate compatibility 
results when a susceptible device fails to perform as  intended due interference from its environment or 
when the device produces unacceptable levels of emission to its enviro nment. This interference is often 
referred to as radio–frequency or electromagneti c interference (RFI/EMI) and can be radiated through 
space or conducted over interconnec ting power of signal cables. In addition to electromagnetic energy, 
EMC also includes possible effects from electrical fields, magnetic fields, electrostatic discharge and 
disturbances in the electrical power supply.
1-4-2 CE Compliance
The LOGIQ™ P5 unit conforms to all applicable c onducted and radiated emission limits and to immunity 
from electrostatic discharge, radi ated and conducted RF fields, magnet ic fields and power line transient 
requirements.
For applicable standards refer to the Safe ty Chapter in the Basic User Manual.
NOTE: For CE Compliance, it is critical that all covers, screws, shielding, gaskets, mesh, clamps, are in  good condition, installed tightly without skew or stress. Proper installation following all 
comments noted in this  service manual is required in order to achieve full EMC performance.
1-4-3 Electrostatic Discharge (ESD) Prevention
WARNINGWARNINGDO NOT TOUCH ANY BOARDS WITH INTEGRATED CIRCUITS PRIOR TO TAKING 
THE NECESSARY ESD PRECAUTIONS: 
1.ALWAYS CONNECT YOURSELF, VIA AN ARM-WRIST STRAP, TO THE ADVISED 
ESD CONNECTION POINT LOCATED ON THE REAR OF THE SCANNER (TO THE 
RIGHT OF THE POWER CONNECTOR). 
2.FOLLOW GENERAL GUIDELINES FOR HANDLING OF ELECTROSTATIC  SENSITIVE EQUIPMENT. 
						

							GE HEALTHCARE
DIRECTION 5394141, REVISION 1LOGIQ™ P5 SEVICE MANUAL 
1-18 Section 1-5 - Customer Assistance
Section 1-5
Customer Assistance
1-5-1 Contact Information
If this equipment does not work as indicated in this service manual or in the User Manual, or if you 
require additional assistance, please contact the lo cal distributor or appropriate support resource, as 
listed below.
Prepare the following information before you call:
- System ID serial number.
- Software version.
Table 1-7    Phone Numbers for Customer Assistance
LocationPhone Number
USA/ Canada
GE Medical Systems
Ultrasound Service Engineering
4855 W. Electric Avenue
Milwaukee, WI 53219
Customer Answer Center 1-800–437–1171
1-800-682-5327
1-262-524-5698
Fax: +1-414-647-4125
Latin America
GE Medical Systems
Ultrasound Service Engineering
4855 W. Electric Avenue
Milwaukee, WI 53219
Customer Answer Center 1-262-524-5300
1-262-524-5698
Fax: +1-414-647-4125
Europe
GE Ultraschall Deutschland GmbH& Co. KG
BeethovenstraBe 239
Postfach 11 05 60, D-42665 Solingen
Germany Tel: +49 212 2802 208
+49 212 2802 207
Fax: +49 212 2802 431
Asia (Singapore/ Japan)
GE Ultrasound Asia
Service Department - Ultrasound
298 Tiong Bahru Road #15-01/06
Central Plaza
Singapore 169730 Tel: +65 291-8528
+81 426-482950
Fax: +65 272-3997
+81 426-482902 
						

							GE HEALTHCARE
DIRECTION 5394141, REVISION 1LOGIQ™ P5 SEVICE MANUAL
Section 1-5 - Customer Assistance 1-19
1-5-2 System Manufacturer
Table 1-8    System Manufacturer
ManufacturerFAX Number
GE Ultrasound Korea
462-120 65-1, Sangdaewon-dong, Joong-won-Gu,
Seongnam-Si, Gyeonggi-do,
Korea82-31-740-6436 
						

							GE HEALTHCARE
DIRECTION 5394141, REVISION 1LOGIQ™ P5 SEVICE MANUAL 
1-20 Section 1-5 - Customer Assistance 
						

							GE HEALTHCARE
DIRECTION 5394141, REVISION 1 LOGIQ™ P5 SERVICE MANUAL
Section 2-1 - Overview 2 - 1
Chapter 2
Pre-Installation
Section 2-1
Overview
2-1-1 Purpose of chapter 2
This chapter provides the information required to plan and prepare for the installation of a LOGIQ™ P5/
A5/A5Pro. Included are descriptions of the facility and electrical needs to be met by the purchaser of the 
unit. A checklist is also provided at the end of this  section to help determine whether the proper planning 
and preparation is accomplished before the ac tual equipment installation is scheduled.
Table 2-1    Contents in Chapter 2
SectionDescriptionPage Number
2-1 Overview 2-1
2-2 General Console Requirements 2-2
2-3 Facility Needs 2-7 
						

							GE HEALTHCARE
DIRECTION 5394141, REVISION  1LOGIQ™ P5 SERVICE MANUAL 
2 - 2 Section 2-2 - General Console Requirements
Section 2-2
General Console Requirements
2-2-1 Console Environmental Requirements 
2-2-1-1 Cooling
The cooling requirement for the LO GIQ™ P5/A5/A5Pro is 2000 BTU/hr. This figure does not include 
cooling needed for lights, people, or other equipment  in the room. Each person in the room places an 
additional 300 BTU/hr. demand on the cooling system.
2-2-1-2 Lighting Bright light is needed for system  installation, updates and repairs. However, operator and patient 
comfort may be optimized if the room light is su bdued and indirect. Therefore a combination lighting 
system (dim/bright) is recommended. Keep in mind that  lighting controls and diameters can be a source 
of EMI which could degrade image quality. These controls should be selected to minimize possible 
interface. Table 2-2    Environmental Requiremen ts for LOGIQ™ P5/A5/A5Pro Scanners
OperationalStorageTransport
Temperature
10 - 30 oC
50 - 104 oF -10 - 60 
oC
14 - 140 oF -40 - 60 
oC
-40 - 140 oF
Humidity30 - 85%
non-condensing 30 - 90%
non-condensing30 - 90%
non-condensing
Pressure700 - 1060hPa 700 - 1060hPa 700 - 1060hPa
Table 2-3    Environmental Requirements for an Ultrasound Room
ItemValues
Power Source
refer to Table 2-4 on page 2-3.
Current Rating7.5A (100V-120V); 3.5A (220-240V) 
Radiation ShieldingNONE REQUIRED for ULTRASOUND ENERGY
Temperature20-26 DEG. C (68-79 DEG F) for PATIENT COMFORT
Humidity50% to 70% for PATIENT COMFORT
Heat Dissipation2000 BTU/Hr. 
Floor Landing Approximately 680 - 800 kg/m2 without Accessories
Floor ConditionGradient: WITHIN 5 degrees
Weight75 kg (165lbs)   without Accessories