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
InnoSight Ultrasound System
Electrical Safety
2 enin
16
P6992-4, EN, 16/12/6
Immunity test
IEC 60601
test level
Compliance
level
Electromagnetic environment - Guidance
Radiated RF
IEC 61-4-3
3 V/m
MHz to
2 GHz
E1 3 V/m
d
P
3
E
1
MHz to MHz
d
P
7
E
1
MHz to 2 GHz
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
a
, should be less than
the compliance level in each frequency range
b
Interference may occur in the vicinity of equipment
marked with the following symbol:
a
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 considered If the measured field strength in the location in which the InnoSight Diagnostic
Ultrasound System is used exceeds the applicable RF compliance level above, the system should be
observed to verify normal operation If abnormal performance is observed, additional measures may be
necessary, such as reorienting or relocating the system
b
Over the frequency range 1 kHz to MHz, field strengths should be less than 3 V/m
To limit exposure to electromagnetic interference from nearby equipment that can degrade image quality,
you should operate the system under EMI conditions that minimize power supply transients, mechanical
interactions, vibration, and thermal, optical, and ionizing radiation
Using cables, transducers, and accessories other than those specified for use with the system
may result in increased emissions from, or decreased immunity of, the system
ME equipment has been tested for radiated RF immunity only at selected frequencies
Separation Distances
The InnoSight Diagnostic Ultrasound System is intended for use in the electromagnetic environment in
which radiated disturbances are controlled The customer or operator of the system can help prevent
electromagnetic interference by maintaining a minimum distance between portable and mobile RF
Communications Equipment and the system as recommended below, according to the maximum output
power of the communications equipment
Maximum
Output Power
of Transmitter
Watts (W)
Separation Distance According to Frequency of Transmitter Meters (m)
1 kHz to MHz
D
3
P
V
1
MHz to MHz
D
3
P
E
1
MHz to 2 GHz
D
P
E
1
1 12 m 12 m 24 m
1 3 m 3 m 4 m
1 11 m 11 m 234 m