Technical Publications

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Rev. 6

LOGIQ™ E10s Release Notes

Software Version R3.x

Operating Documentation
Copyright© 2021 By General Electric Co.
Regulatory Requirement

This product complies with regulatory requirements of the 2017/745 EU Medical

Device Regulation concerning medical devices.

First CE Marked in 2021.

This manual is a reference for the LOGIQ E10s. It applies to all versions of
Software Version R3 Revision x.x for the LOGIQ E10s ultrasound system.

GE
P.O. Box 414, Milwaukee, Wisconsin 53201 U.S.A.
(Asia, Pacific, Latin America, North America)

GE Healthcare GmbH
Beethovenstrasse 239
Postfach 11 05 60
D-42655 Solingen GERMANY
TEL: 49 212.28.02.208; FAX: 49 212.28.02.380
Revision History
Reason for Change

DATE
REV (YYYY/MM/DD) REASON FOR CHANGE

Rev. 2 2021/07/06 Initial release

Rev. 3 2021/09/09 FDA Update

Rev. 4 2021/11/23 Version R3 Revision 1.x Updates

Rev. 5 2022/02/09 CH-REP Update

Rev. 6 2022/04/05 Remove EAC from Table 1-3.

List of Effective Pages

REVISION REVISION
PAGE NUMBER NUMBER PAGE NUMBER NUMBER

Title Page Rev. 6 Regulatory Requirements Rev. 6

Revision History Rev. 6 Notes and Workarounds Rev. 6

Please verify that you are using the latest revision of this document. Information
pertaining to this document is maintained on MyWorkshop. If you need to know the latest
revision, contact your distributor, local GE Sales Representative or in the USA call the
GE Ultrasound Clinical Answer Center at 1 800 682 5327 or 1 262 524 5698.

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Regulatory Requirements

Authorized EU Representative
European registered place of business:
GE Medical Systems SCS
283 rue de la Minière
78530 BUC, France

Authorized Swiss Representative

GE Medical Systems (Schweiz) AG
Europa-Strasse 31
8152 Glattbrugg
Switzerland

Manufacturer
GE Ultrasound Korea, Ltd.
9, Sunhwan-ro 214beon-gil, Jungwon-gu, Seongnam-si,
Gyeonggi-do,
KOREA

Full Listing
For a full listing of regulatory requirements, see the LOGIQ E10s
Basic User Manual, Direction 5860662-1xx.

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 Chapter 1

LOGIQ E10s R3.x

Release Notes

ATTENTION LOGIQ E10s USERS:

This document contains information concerning the

use of your LOGIQ E10s ultrasound system.
Precautions and instructions are included that
supplement the Basic User Manual and address
specific concerns related to the software versions
cited above. Keep this document with the Basic
User Manual and have all users become familiar
with its contents and organization before using
your system under these software versions.

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LOGIQ E10s R3.x Release Notes

Addendum

Overview
The content in these Release Notes includes an Addendum to
the Basic User Manual, Direction 5860662-1xx. Important
system Notes and Workarounds are also provided. Information
included in these Release Notes supersedes Basic User Manual
and Basic Service Manual content.

Updates to the Basic User Manual

The following are updates/changes to the Basic User Manual:
• Manual Probe Test
• Restore Region Imaging Presets
• B-Flow Visualization Probes
• Strain Elastography Clinical Applications
• System Data - Depth
• Measurement Bias Information Tables - ML4-20-D/
ML4-20VN-D
• Device Labels
• Wireless LAN (WLAN) Specifications
• Preset Restore User Interface Corruption
• Reusable Accessory Cleaning

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 Addendum

Manual Probe Test

When “Enable Automatic Probe Diagnostics” is selected on the
Utility->Admin page, the Probe Test utility appears on the
B-Mode Touch Panel Page 2 (see Figure 1-1). (The Probe Test
utility does not appear while Scan Assistant is running.) A
manual probe test can be run with this utility on the following
probes: C1-6-D, IC5-9-D, M5Sc-D, ML6-15 and RIC5-9-D.

Figure 1-1. Probe Test

Run Probe Test

Ensure the probe lens surface is clean and free of dirt, water or
coupling gel before beginning probe test.
1. Select the Probe Test button on the Touch Panel (see
Figure 1-1).
2. A pop-up appears specifying to ensure the probe lens
surface is clean. If the lens is clean, select Yes on the
pop-up (see Figure 1-2). The probe test takes approximately
5 to 10 seconds.

Figure 1-2. Probe Test Pop-up

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LOGIQ E10s R3.x Release Notes

Run Probe Test (continued)

3. When the probe test is complete, a pop-up displays

specifying if the probe “Passed” (1) or “Failed” (2) the test
(see Figure 1-3). If the probe passed the test, continue
using the probe. If the probe failed the test, follow the
instructions on the pop-up.

Figure 1-3. Probe Test Pass or Fail Pop-ups

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 Addendum

Restore Region Imaging Presets

The LOGIQ E10s R3 system supports only two region imaging
presets: Europe and None. LOGIQ E10s R2 region presets are
not transferred to the LOGIQ E10s R3 if the presets were
configured on the R2 system as: Americas, China, Europe or
Japan.
• R2 imaging presets configured as Americas, China or Japan
do not transfer to R3 imaging presets.
• R2 imaging presets configured as Europe do not transfer to
R3 imaging presets configured as Europe. The R3 Europe
default imaging presets will remain.
When restoring imaging presets using Detailed Restore, if the
pop-up message below appears, the imaging settings from R2
regional imaging presets are not compatible with R3 and will not
be transferred.

Figure 1-4. Region Preset Error

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LOGIQ E10s R3.x Release Notes

B-Flow Visualization Probes

The note below contains the updated list of probes available for
B-Flow Visualization:
NOTE: Available for C1-6-D, C1-6VN-D, C2-9-D, C2-9VN-D, L2-9-D,
L2-9VN-D, L3-12-D, ML4-20-D, ML4-20VN-D, L6-24-D,
L8-18i-D, M5Sc-D, C3-10-D, C2-7-D, C2-7VN-D and ML6-15-D
probes.

Strain Elastography Clinical Applications

The table below updated probes for the Breast and MSK
applications:

Table 1-1: Clinical Applications

Application Compare the suspicious lesion with: Probe

Breast A fatty area in the breast or the average rounding • L2-9-D/L2-9VN-D

breast tissue. • L8-18i-D
• ML4-20-D/ML4-20VN-D
• ML6-15-D
• L3-12-D

MSK A normal area in the same part of the body. • C1-6-D/C1-6VN-D

• C2-9-D/C2-9VN-D
• L2-9-D/L2-9VN-D
• L8-18i-D
• L3-12-D
• ML4-20-D/ML4-20VN-D
• ML6-15-D

System Data
The table below is updated with actual system depth:

Features/Specifications
Table 1-2: Physical Attributes

Dimensions and Weight (for Transport)

• Height: 1300mm, 51 in
• Width: 585mm, 23 in
• Depth: 900.9mm, 35.5 in
• Weight (with HDU monitor): 118 kg, 260 lb.
• Weight (with OLED Monitor): 115 kg, 254 lb.

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 Addendum

Device labels
The Multi Caution Label and Rating plate are changed in
Figure 1-5, with a description in Table 1-3. (Reference the
“Device Labels” section in Chapter 2 of the Basic User Manual
for more information.)

Figure 1-5. Rear Panel Label Location

Label Icon Description

Table 1-3: Label Icons (Rear of Console)

Item Label/Icon Purpose/Meaning

1. GE Cares Label (US/Canada systems only)

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Table 1-3: Label Icons (Rear of Console) (Continued)

Item Label/Icon Purpose/Meaning

2.
Monitor Label:
GE created

How to lock system prior to transport

DO NOT place a finger, hand or any object on the joint of the

monitor or monitor arm to avoid injury when moving the monitor
and monitor arm.

3. United States only

Prescription Device label
21 CFR 801.109 and Alternative to Certain Prescription Device
Labeling Requirements Guidance to Industry 1/2/2000 U.S.
Food&Drug Administration modified by General Electric for
clarity that this is for the USA

4. UL conformity mark according to ANSI/AAMI ES60601-1:2005/

(R)2012, CAN/CSA-C22.2 No. 60601-1:14.
N/A- by certification body

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 Addendum

Table 1-3: Label Icons (Rear of Console) (Continued)

Item Label/Icon Purpose/Meaning

5. RoHS Label–China China Electronic Industry Standard SJ/T11364-2014

systems only (shown for Indicates the presence of hazardous substance(s) above the
country specific label) maximum concentration value. Maximum concentration values
for electronic information products, as set by the People’s
Republic of China Electronic Industry Standard SJ/T11364-2006,
include the hazardous substances of lead, mercury, hexavalent
chromium, cadmium, polybrominated biphenyl (PBB), and
polybrominated diphenyl ether (PBDE). “20” indicates the
number of years during which the hazardous substance(s) will
not leak or mutate so that the use of this product will not result in
any severe environmental pollution, bodily injury, or damage to
any assets.

Indicates the presence of hazardous substance(s) above the

maximum concentration value. Maximum concentration values
for electronic information products, as set by the People’s
Republic of China Electronic Industry Standard SJ/T11364-2006,
include the hazardous substances of lead, mercury, hexavalent
chromium, cadmium, polybrominated biphenyl (PBB), and
polybrominated diphenyl ether (PBDE). “10” indicates the
number of years during which the hazardous substance(s) will
not leak or mutate so that the use of this product will not result in
any severe environmental pollution, bodily injury, or damage to
any assets.

6. Follow instruction for use.

IEC 60601-1:2005+A1:2012 Annex D.1 and ISO 7010-M002

7. “General Warning Sign”

Possible shock hazard. Do not remove covers or panels. No
user serviceable parts are inside. Refer servicing to qualified
service personnel. Standard: ISO 7010-W001.

8. Use two people to transport system on inclines.

To avoid possible injury and equipment damage when
transporting from one area of use to another:
• Be sure the pathway is clear.
• Limit movement to a slow careful walk.
• Use two or more persons to move the equipment on inclines or
long distance.

GE created

9. This WEEE symbol indicates that waste electrical and electronic

equipment must not be disposed of as unsorted municipal waste
and must be collected separately. Please contact an authorized
representative of the manufacturer for information concerning
the decommissioning of your equipment. Standard: EN 50419.

WEEE Directive 2012/19/EU

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Table 1-3: Label Icons (Rear of Console) (Continued)

Item Label/Icon Purpose/Meaning

10. Type BF Applied Part (man in the box) symbol is in accordance

with IEC 60417-5333.

11. This product is a medical device.

12. Symbol indicating that the Instructions for Use are supplied in
electronic form.
ISO 7000-3500

13. Do not use the following devices near this equipment: cellular
phone, radio receiver, mobile radio transmitter, radio controlled
toy, broadband power lines, etc. Use of these devices near this
equipment could cause this equipment to perform outside the
published specifications. Keep power to these devices turned off
when near this equipment.

ISO 7010-P013

14. DO NOT push the system. Use the handle to push/pull the
system, e.g., DO NOT use the monitor. Failure to do so may
cause serious injury or system damage.

IEC 60601-1:2005+A1:2012 Annex D.2 and ISO 7010-P017

15. The CE Mark of Conformity indicates this equipment conforms

with the European Medical Device Regulation 2017/745

European Medical Device Regulation 2017/745

16. Authorized European Representative address

The CH-REP label indicates the authorized representative in

Switzerland.

17. The MR Unsafe label is to warn that this Ultrasound System

poses risks to the patient, medical staff or other persons within
the MR environment and that the Ultrasound system should
remain outside of the MR environment.

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 Addendum

Table 1-3: Label Icons (Rear of Console) (Continued)

Item Label/Icon Purpose/Meaning

18. Federal Communications Commission Identification label - on

LOGIQ E10s equipped with Wireless LAN

Non-Ionizing Electromagnetic Radiation

IEC 60417-5140
IEC TR 60878-5140

Federal Communications Commission Identification label - on

LOGIQ E10s equipped with Wireless LAN

Canada Certification label - on LOGIQ E10s equipped with

Wireless LAN

Malaysian Communications and Multimedia Commission

symbol. Number correspond to GE importing company (GEHC) -
on LOGIQ E10s equipped with Wireless LAN

ANATEL Certification label for Brazil - on LOGIQ E10s equipped

with Wireless LAN

Infocomm Development Authority of Singapore (IMDA) standard

- on LOGIQ E10s equipped with Wireless LAN

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Table 1-3: Label Icons (Rear of Console) (Continued)

Item Label/Icon Purpose/Meaning

19. Possible shock hazard. Do not remove covers or panels. No

user serviceable parts are inside. Refer servicing to qualified
service personnel.
• USB 3.0 Ports
• Ethernet Connection
• S-Video Connector
• HDMI Connector

“Equipotentiality” indicates the terminal to be used for connecting

equipotential conductors when interconnecting (grounding) with
other equipment.
Connection of additional protective earth conductors or potential
equalization conductors is not necessary in most cases and is
only recommended for situations involving multiple equipment in
a high-risk patient environment to provide assurance that all
equipment is at the same potential and operates within
acceptable leakage current limits. An example of a high-risk
patient would be a special procedure where the patient has an
accessible conductive path to the heart such as exposed cardiac
pacing leads. IEC60417-5021
IEC 60601-1:2005+A1:2012 Annex D.1 and IEC 60417-5021

Mains OFF: indicates the power off position of the mains power
breaker.
IEC 60601-1:2005+A1:2012 Annex D.1 and IEC 60417-5008

Mains ON: indicates the power on position of the mains power

breaker.
IEC 60601-1:2005+A1:2012 Annex D.1 and IEC 60417-5007

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Table 1-3: Label Icons (Rear of Console) (Continued)

Item Label/Icon Purpose/Meaning

20. Every system has a unique marking for identification, the Unique
Device Identification (UDI) Label. The UDI label consists of a
series of alpha-numeric characters and barcode which uniquely
identify the LOGIQ E10s system as a medical device
manufactured by General Electric. Scan or enter the UDI
information into the patient health record as required by
country-specific laws.

UDI Human Readable Label Text: Global Trade Item Number,

GTIN, Manufacturing Date, Serial Number

UDI Symbol and Data Matrix

System Voltage (~100-240VAC)

Frequency
Power Rating

Alternating Current symbol is in accordance with IEC

60417-5032

Catalog/Model Number. Standard: ISO 7000-2493.

Serial Number. Standard: ISO 7000-2498.

Legal Manufacturer’s name and address. Standard: ISO

7000-3082.

Date of manufacture YYYY-MM. Standard: ISO 7000-2497.

The CE Mark of Conformity indicates this equipment conforms

with the European Medical Device Regulation 2017/745

European Medical Device Regulation 2017/745

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LOGIQ E10s R3.x Release Notes

Measurement Bias Information Tables

The ML4-20-D/ML4-20VN-D Measurement Bias Information
Tables are added below. (Reference the “Shear Wave
Elastography” section in Chapter 13 of the Basic User Manual
for more information.)

Figure 1-6. ML4-20-D/ML4-20VN-D Measurement Bias Information (Velocity on the left

and Stiffness on the right)

Wireless LAN (WLAN) Specifications

Intel declaration of conformity
You can find the Intel Declaration of Conformity at this web link:
https://www.intel.com/content/dam/support/us/en/documents/
network-and-i-o/wireless-networking/
9260NGW-EU-RED-DoC.pdf

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 Addendum

Preset Restore User Interface Corruption

When restoring presets with the user interface in Russian,
Greek, Japanese or Simplified Chinese, if the OS Region
Language does not match the selected system software
application language at the time of the preset restore, the user
interface text may appear corrupted.
To prevent the corruption, before restoring presets, confirm that
the OS Region language and system software application
language match by following the procedure below, ‘Match the
OS Language with System Software Application Language’ on
page 1-15, referring to Figure 1-7.
If the corruption has already occurred and the text on the screen
is not readable, follow the same procedure (‘Match the OS
Language with System Software Application Language’ on
page 1-15) to correct the settings, referring to Figure 1-8, which
shows the location of the Regional Options and Language fields
on the corrupted screens.

Match the OS Language with System Software Application Language

Change the default operating system language on the Utility >

System > General page.
1. Select Regional Options to open the Regional Options
dialogue box (1).
2. Select Current OS Language and select the OS language
from the dropdown menu to match the system language (2).
3. Select OK (3). The system will restart.

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LOGIQ E10s R3.x Release Notes

Match the OS Language with System Software Application Language

(continued)

Figure 1-7. Match OS Language with System Software

Application Language (Preventative)

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 Addendum

Match the OS Language with System Software Application Language

(continued)

Figure 1-8. Match OS Language with System Software

Application Language (Corrective)

Reusable Accessory Cleaning

DANGER Reusable accessories should be cleaned and disinfected or

sterilized as stated by the manufacturer, after each patient
examination.

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LOGIQ E10s R3.x Release Notes

Notes and Workarounds

Please become familiar with the following Notes and

Workarounds (Workarounds assume that the print keys are set
up with P1 as raw data and P4 as screen capture):
Important to Performance and Data Integrity - Identifies
issues that are Important to Performance and Data Integrity. A
failure to follow these instructions can result in seriously
impaired function.
Notes and Workarounds and Feature Limitations - Identifies
Notes and Workarounds and Feature Limitations, where
unavailable features may result in a loss of some functionality
and cause some user inconvenience.
Additional Notes and Workarounds - Identifies Additional
Notes and Workarounds, providing information on issues you
may encounter while performing scans and offers workarounds
for these issues.
Connectivity Notes and Workarounds - Identifies Connectivity
Notes, Workarounds, and General Information.

WARNING The LOGIQ E10s is not intended to be used as a storage

device; the backup of the Patient and Image Database is your
institution’s responsibility. GE is NOT responsible for any lost
patient information or for lost images.

Important to Performance and Data Integrity

No workarounds for performance or data integrity.

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 Notes and Workarounds

Notes and Workarounds and Feature Limitations

Table 1-4: Notes and Workarounds and Feature Limitations

Category Note/Workaround

4D CINE If you export a 4D CINE Loop formatted as Enhanced DICOM, these CINE
Loops will be exported as single JPEG images. Instead, use default Standard
DICOM with Raw Data.

Auto TGC If TGC on recalled images is adjusted in dual view, when switching between
L/R the TGC curve will appear the same but not apply to the new image.
Adjust the TGC on the new image, if needed.

Comments If you annotate an image while in Doppler Mode and then exit Doppler Mode,
the Comment may not be able to be edited. It can be deleted, but not
repositioned or edited.

Compare Assistant Only 1 CINE clip can be stored while active in Compare Assistant. Dual CINE
clip storage is unavailable while in Compare Assistant.

Compare Assistant - 3D Compare Assistant is not available while performing a 3D Sweep.

Sweep

Compare Assistant and Compare Assistant is not available while using Micro Vascular Imaging in PDI
MVI Mode.

MVI and QAnalysis QAnalysis is not available for MVI.

Pulsed Wave Sample The PRF may increase/decrease unexpectedly when moving the Sample
Volume + Depth Change Volume Gate to different depths and adjusting the PRF to maximum.

Dual View For frozen and recalled images, the grayscale appearance on the left side of
the image has a higher contrast grayscale appearance while in DualView.

M-Mode Cursor The M-Mode Cursor Angle changes when recalling a zoomed M-Mode
image.

Large CINE Clips Large CINE Raw Data Clips (>30 seconds) are not transferring to PACS. The
workaround is to compress images on the button setting.

Contrast When going between Dual view and Single view in the Contrast package, the
noise level may adjust. Change the overall gain to adjust the noise level as
needed.

RIC5-9 Max Angle When going to Max angle using the RIC5-9 probe, the gain may change. If
this happens, adjust the gain manually, as needed.

Scan Assistant Creator Scan Assistant Creator may lock up with a session timeout of one minute. If
this issue happens, press ESC; or, if possible, exit out of Scan Assistant
Creator when not using it to prevent this issue.

Dual Screen In Dual Screen, gain may not adjust as expected. If this happens, adjust the
gain prior to going into a Dual Screen image.

Compare Assistant When recalling a Dual screen PW image in Compare Assistant, the Dual
image may not recall as expected.

B Mode If system is rebooted with no probe connected, Contrast may not appear as
expected. When booting up system, ensure a probe is connected.

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Table 1-4: Notes and Workarounds and Feature Limitations (Continued)

Category Note/Workaround

Privacy and Security If invalid password entered three times for Administrator logon, user is
blocked from logon for three minutes, but no message displays notifying the
blocked status (only an “Invalid Credentials” message will display).

UGAP The appearance of a Gray Scale image may appear with excessive contrast
for one second when exiting the UGAP feature on the system.

V Nav If more then one 3D US is loaded from the database, the volume label will be
incorrect and the image settings may be incorrect. Do not load more than one
3D US volume from the database.

V Nav CT/MR data cannot be loaded when a folder (or any file not related to
DICOM) exists in the same folder the DICOM file is loaded from. Ensure the
folder that is uploaded into the system has only DICOM data in the folder.

Stress Echo The grid size in Select Cycles screen may change without user input. If this
happens, press [Select Later] on touch panel or on the screen, then press the
Protocol tab and click the [Select Cycles] button. This will not work in the
case where the buffer reaches 100%.

Volume Review After acquiring a Static 3D image and recalling it from the clipboard, going
into Volume Review may show only a single sectional plane image. To
activate Volume Review, select the Static 3D tab and Volume Review again,
and the clip will play.

Beta View The Beta View image may not be centered if the Beta View value is set below
0. If this happens, reset the Beta View value to 0.

Beta View Changing Beta View angle repeatedly and frequently may cause “No
machine motor controller” error. To prevent this, change Beta View angle
slowly.

Connectivity Color images sent to PACS may display with a different color gain if
Multiframe is not selected in Utility-Connectivity-Button. Use Checkbox to
select Multiframe, or Use Direct Store in Data flow.

Image Recall When CINE loop with TIC ROI stored from TIC analysis is recalled, ROI
graphics may disappear. Instead, recall TIC loop.

Compare Assistant If Easy 3D is not exited prior to entering Compare Assistant, the control
information and comparison clipboard may not display correctly. Ensure Easy
3D is exited prior to entering Compare Assistant.

PACS If Send to PACS fails with “Server cannot receive color data” error, go to
DICOM Service, deselect UseButtonSetting and change the Color Support
from “Mixed” to “Color.”

PACS If the color map of a Contrast image becomes gray in PACS when stored
using Still Capture, go to DICOM Service, deselect UseButtonSetting and
change the Color Support from “Mixed” to “Color.”

V Nav Images to PACS When storing VNAV images to PACS, confirm that all images display
correctly on PACS. If the images are not displayed correctly on PACS, store
the images from the system to USB first and then transfer from USB to
PACS.

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Table 1-4: Notes and Workarounds and Feature Limitations (Continued)

Category Note/Workaround

Contrast MVI When Mark Cine is pushed in Contrast MVI, the gain of the background
B-Mode image may change. Changing the gain again will reset it to the
correct value.

Wireless LAN When the LAN is disconnected during a DICOM request, the network may
not switch automatically from the LAN to the Wireless LAN. Verify in the
Spooler that a DICOM transfer is completed before switching from Wired LAN
to Wireless LAN.

Report Writer In Designer Mode, the configured text color you configured is not applied.

Backup Preset backup to CD may not function correctly; instead, backup presets to a
USB flash drive.

3D/4D In 3D/4D pre mode, if part of the image is missing, disconnect and reconnect
the probe and start scan again to obtain full image.

C2-9(VN)-D Probe UGAP is not supported for Abdomen on the C2-9(VN)-D probe.

V Nav If the CT image is reversed when loading the 3D Volume dataset, re-register
on the system to correct the image.

PW When changing modes, the sweep speed may reset. Reselect the desired
sweep speed.

Main Display Monitor Confirm the main display monitor is locked in position before moving system.

Start Assistant When storing a patient screen image, Start Assistant may not activate as
expected. In this case, manually select the probe and application.

IP Address If the IP address is not set after a software reload, please reconnect the
system to the wireless or wired connection.

Single Image Print Single Image Print setting may result in a Cine clip store after using digital
TGC. To prevent, do not push freeze and print in rapid succession.

Printers If you have two printers connected that are the same type of printer, the
LOGIQ E10s only recognizes one of the printers. Only plug in one printer in
this case.

DICOM If Send To is not available on the Touch Panel, select Send To from the Active
Images screen.

MPEGvue Saving data to MPEGvue may cause an unexpected system shutdown. Do

not save multiple exams to MPEGvue.

V Nav When storing V Nav images to a PACS device, confirm that all images
display on the PACS device. If the images are not displayed correctly on the
PACS device, store images from the system to a USB drive, then transfer
from the USB drive to the PACS device.

Zoom Entering Zoom before starting 3D/4D may distort the ROI shape and
behavior. Do not enter Zoom before starting 3D/4D.

Probe Port If no image appears after a probe is connected to probe port, connect the
probe to a different probe port.

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Table 1-4: Notes and Workarounds and Feature Limitations (Continued)

Category Note/Workaround

Image Annotation When transitioning from single screen to dual screen, the annotation may
move. If this happens, manually move the annotation to the desired position.

Query/Retrieve If the LAN cable is unplugged while a Query/Retrieve is in process, the dialog
box may display as blank for 5-10 seconds. Do not unplug the LAN cable
from system when a Query/Retrieve is in progress.

Scan on Battery If the battery is too low, the system may not go into power saving mode
during Scan on Battery and the system may shut down unexpectedly.
Connect the system to the A/C power supply to recharge when battery is low.

Keyboard Lock The Keyboard Lock dialog box may not be visible after locking the system for
cleaning. If this happens, use the unlock rotary to unlock.

Worklist Disconnecting from the network while the Worklist is actively retrieving
patient data may cause the system to freeze. Do not disconnect the network
cable while querying the worklist.

Virtual Convex When using Virtual Convex, the MVI ROI may decrease in size suddenly
when moved too deep in the far field. If this happens, exit MVI and enter PDI
or Color Flow to correct.

Virtual Convex If Virtual Convex is turned off and then back on, the MVI ROI may increase in
width. To prevent, do not turn Virtual Convex off and back on.

Image Annotation Using special characters in user created annotations may cause the
comments to not display on the touch panel. When creating comment
libraries, do not use special characters (other than letters and numbers).

Footswitch If the footswitch is used when Scan on Battery is on in Power Assistant

mode, functions such as Freeze may not work as expected. Do not use the
footswitch while using Scan on Battery.

DICOM SR When performing DICOM SR and measure method is last, if last taken
measurement is deleted, take measurement again.

Static 3D + PDI Static 3D Sweep while in PDI may be interrupted. To correct, restart the scan
or acquire 2D with PDI.

PACS When using Push from PACS and sending a previous patient exam, the
exam list may not be refreshed with the newly received exam. To correct, exit
the patient exam and reselect the patient.

Patient Data Archiving If the transfer of patient data to media operation was cancelled, check the
media to confirm that the data did not transfer.

1-22 LOGIQ E10s – Release Notes

Direction 5862474 -1EN English Rev. 6
 Notes and Workarounds

Table 1-4: Notes and Workarounds and Feature Limitations (Continued)

Category Note/Workaround

CINE Image Save to USB If the system shows the error “Saving Image to DICOM Media Failed. Not
enough space on Media,” check the clipboard and confirm that the image
was saved. If the image was not save as intended, reacquire the image using
new media with enough free space to save the image.

MyPreset Shortcuts When returning to Scan screen after deleting a preset, that deleted preset
may show up on the Touch Panel without the corresponding image. To
correct, select another preset and continue scanning.

Power Assistant If multiple power losses in short duration (less than one second) occur, the
system will enter Power Assistant mode and may not recognize the AC
recovery power. To recover, unplug the system from AC power for more than
one second.

LOGIQ E10s – Release Notes 1-23

Direction 5862474 -1EN English Rev. 6
LOGIQ E10s R3.x Release Notes

1-24 LOGIQ E10s – Release Notes

Direction 5862474 -1EN English Rev. 6