User's Manual
Table Of Contents
- 1 Read This First
- 2 Safety Information
- 3 Overview
- 4 Preparing the System
- Inserting a microSD Card
- Using the Stand
- Charging the System
- Connecting the Transducer
- Removing the Transducer
- Using the System On The Go
- Using the Wheel Brakes
- Placing the Transducer Holder
- Mounting the System to the System Cart
- Adjusting the System Cart Height
- Connecting an External Printer
- Tilting the System
- Unmounting the System From the System Cart
- Moving the System
- Outputting the System Display to an HDMI-Enabled TV or Monitor
- Supported External Printers
- 5 Using the System
- Turning On/Off the System
- Logging Into the System
- Launching the Main Screen
- Setting the System Time and Date
- Controlling the System
- Setting the System Language
- Identifying the Main Screen Layout
- Switching the Control Panel Pages
- Managing the System Power
- Managing Disk Space
- Network Configuration
- DICOM Configuration
- 6 Performing an Exam
- Starting a New Exam
- Adding a New Patient
- Loading a Worklist
- Selecting a Preset
- Setting the Transducer Orientation
- Selecting/Switching a Scan Mode
- Adjusting the Displayed Image
- Freezing an Image
- Adding Annotations
- Adding Measurements
- Saving and Printing the Image
- Reviewing the Image
- Exporting the Exam
- Managing the Exam List
- Ending the Exam
- 7 Using Image Controls
- 2D Mode Image Controls
- Overview
- Adjusting Gain
- Adjusting Frequency
- Adjusting Time Gain Compensation (TGC)
- Adjusting the Scan Depth
- Adjusting the Focus Depth, Focal Zone and Focal span
- Adjusting Dynamic Range
- Using Tissue Harmonic Imaging (THI)
- Adjusting Persistence
- Adjusting Sharpness and Smoothing
- Adjusting Gray Map
- Adjusting Chroma Map
- Adjusting Steer Angle
- Adjusting the Sector Width and Position
- Adjusting Power
- Using Trapezoidal Imaging
- Adjusting Density
- Using Compound Imaging
- Using ENV (Enhanced Needle Visualization)
- Color/CPA Mode Image Controls
- M-Mode Image Controls
- Spectral Doppler Mode Image Controls
- 2D Mode Image Controls
- 8 System Customization and Service
- Customizing Your System
- Configuring Security Policies
- Servicing your system
- Reinstalling Software
- Checking the Software Version
- Checking the System’s Serial Number
- Checking the Tablet’s Serial Number
- Checking the License Status
- Resetting User Settings
- Backing Up System Settings and Patient Data
- Restoring System Settings and Patient Data
- Resetting Your System
- Testing the System
- Exporting System Logs
- Reading the User Manual
- 9 Transducers
- 10 Transducer Care
- 11 System Maintenance
- 12 Appendix
1
2 enin
Electrical Safety
InnoSight Ultrasound System
P6992-4, EN, 16/12/6
Emissions test Compliance Electromagnetic environment - Guidance
RF Emissions CISPR 11 Class B The InnoSight Diagnostic Ultrasound System is suitable for
use in all establishments, including domestic, and those
directly connected to the public low-voltage power supply
network that supplies buildings used for domestic purposes
Harmonics IEC 61-3-2 Class A or B
Flicker IEC 61-3-3 Complies
RF Emissions CISPR 14-1 Complies The InnoSight Diagnostic Ultrasound System is not suitable
for interconnection with other equipment
RF Emissions CISPR 1 Complies The InnoSight Diagnostic Ultrasound System is not suitable
for interconnection with other equipment
Guidance and Manufacturer’s Declaration - Electromagnetic Immunity - All Equipment
Immunity test
IEC 60601 test
level
Compliance
level
Electromagnetic environment - Guidance
ESD
IEC 61-4-2
6 kV Contact
kV Air
As specified Floors should be wood, concrete or ceramic
tile If floors are synthetic, the relative humidity
should be at least 3
EFT
IEC 61-4-4
2 kV Mains
1kV I/Os
As specified Mains power quality should be that of a typical
commercial or hospital environment
Surge IEC 61-4- 1 kV Differential
2 kV Common
As specified
Voltage dips/
Dropout IEC 61-
4-11
9 dip for
cycle
6 dip for
cycles
3 dip for 2
cycles
9 dip for
seconds
As specified Mains power quality should be that of a typical
commercial or hospital environment If the user
of the InnoSight Diagnostic Ultrasound System
requires continued operation during power
mains interruptions, it is recommended that
the InnoSight Diagnostic Ultrasound System be
powered from an uninterruptible power supply
or battery
Power frequency
/6 Hz
Magnetic field
IEC 61-4-
3 A/m As specified Power frequency magnetic fields should
be that of a typical commercial or hospital
environment
Guidance and Manufacturer’s Declaration - Electromagnetic Immunity - Non-life-supporting Equipment
Immunity test
IEC 60601
test level
Compliance
level
Electromagnetic environment - Guidance
Portable and mobile RF communications equipment
should be used no closer to any part of the InnoSight
Diagnostic Ultrasound System, including cables, than the
recommended separation distance calculated from the
equation applicable to the frequency of the transmitter
Recommended separation distance
Conducted RF
IEC 61-4-6
3 Vrms
1 Hz to
MHz
V1 3 Vrms
d
P
3
V
1