GE Logiq P5 User Manual

Safety Precautions
LOGIQ 5 Basic User Manual 2-23
Direction 2300002-100 Rev. 2
Patient Environmental Devices
 Figure 2-1. Patient Environmental Devices
100-120V  150VA Max12
3
45
86
7
9
10
11
15
16
17
12
18
19
1320
1421
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25 

Safety
2-24 LOGIQ 5 Basic User Manual
Direction 2300002-100 Rev. 2
Patient Environmental Devices (continued)
1.  Peripheral Device (Signals I/O Port, Power In)
2.  Front Panel (Signal I/O Port, Power Out)
3. Non-Imaging Probes
4. Imaging Probes
5. Probe Port
6. ECG Cable
7. PCG Sensor
8. Physio-Signal Input Panel
9. Rear Panel
10.  Signals I/O Port
11 .  P o w e r  O u t
12.  Signals I/O Port
13. Footswitch Connector
14. Power In
15. Peripheral Devices
16.  Signals I/O Port
17. Power In
18.  InSite Modem...

Safety Precautions
LOGIQ 5 Basic User Manual 2-25
Direction 2300002-100 Rev. 2
Acceptable Devices
The devices shown in Figure 2-1 are specified to be suitable for 
use within the PATIENT ENVIRONMENT.
Unapproved Devices
Accessories, Options, Supplies 
CAUTIONDO NOT connect any probes or accessories without approval 
by GE within the PATIENT ENVIRONMENT.
See ‘Peripheral Update for EC countries’ for more information.
CAUTIONThe unapproved devices shall be used out of patient 
environment.
If devices are...

Safety
2-26 LOGIQ 5 Basic User Manual
Direction 2300002-100 Rev. 2
Acoustic Output
Located on the upper right section of the system display monitor, 
the acoustic output display provides the operator with real-time 
indication of acoustic levels being generated by the system. See 
the Acoustic Output chapter in the Advanced Reference Manual 
for more information. This display is based on NEMA/AIUM 
Standards for Real-time Dispaly of Thermal and Mechanic 
Acoustic Output Indices on Diagnostic Ultrasound...

Safety Precautions
LOGIQ 5 Basic User Manual 2-27
Direction 2300002-100 Rev. 2
Controls Affecting Acoustic Output
The potential for producing mechanical bioeffects (MI) or 
thermal bioeffects (TI) can be influenced by certain controls. 
Direct. The Acoustic Output control has the most significant 
effect on Acoustic Output. 
Indirect. Indirect effects may occur when adjusting controls. 
Controls that can influence MI and TI are detailed under the 
Bioeffects portion of each control in the Optimizing the...

Safety
2-28 LOGIQ 5 Basic User Manual
Direction 2300002-100 Rev. 2
Warning Label Locations
Console Labels
 Figure 2-2. Label Location (a)
1.  Caution for Possible Injury: “Never put any device onto the 
Monitor.
2.  Caution for Hazardous movement (attached inside of OP 
rear cover).
3.  Defibrillator Label: “Do not use with Defibrillator” (attached 
on optional ECG).
(1)
(2)
(3) 

Safety Precautions
LOGIQ 5 Basic User Manual 2-29
Direction 2300002-100 Rev. 2
Console Labels (continued)
 Figure 2-3. Label Location (b)
220-240V  500VA MaxIncluding front printer panel
100~120V  500VA MaxIncluding front printer panel
Japan/USA/Asia Console (100~120V) Europe/USA Console (220V)
(1)
(3)
(4)
(5)
(6)
(2)
(7)
AC Line Input
Circuit Breaker
100-120V~ 50/60HzOn
Off 1250VA Max
I
AC Line InputCircuit Breaker220-240V~ 50/60HzOn
Off 1250VA Max
Ior (8)(9) 

Safety
2-30 LOGIQ 5 Basic User Manual
Direction 2300002-100 Rev. 2
Console Labels (continued)
Table 2-8: Label Location Explanations
1.  Possible shock hazard. Do not 
remove covers or panels. No user 
serviceable parts are inside. Refer 
servicing to qualified service 
personnel.
2.  Do not use the following devices near 
this equipment: cellular phone, radio 
receiver, mobile radio transimitter, 
radio controlled toy, etc. Use of these 
devices near this equipment could 
cause this equipment to perform...

Safety Precautions
LOGIQ 5 Basic User Manual 2-31
Direction 2300002-100 Rev. 2
Console Labels (continued)
 Figure 2-4. ETL and Identification/Rating Plate Label Location (c)
Korea 220V Console
(1)(2)
(3)
(4)
(5) (6)
GE MEDICAL SYSTEMS KOREA LTD.
LOGIQ 5
1250VA
1250VA
1250VA120V5
GE Medical Systems Korea GE MEDICAL SYSTEMS KOREA LOGIQ 5 

Safety
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Direction 2300002-100 Rev. 2
Console Labels (continued)
1.  ETL Label: NRTL Listing and Certification Mark is used to 
designate conformance to nationally recognized product 
safety standards.
2.  Identification and Rating Plate–USA/Asia 120V Console.
3.  Identification and Rating Plate–Europe/Asia/Latin America 
220V Console.
4.  Identification and Rating Plate–Japan 120V Console.
5.  Identification and Rating Plate–Korea 220V Console.