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
14
P6992-4, EN, 16/12/6
Battery Usage/Disposal
Do not disassemble the system
Use only the supplied battery Using an unapproved battery may cause the system to explode
and result in serious damage to your health or property
Do not replace, heat, crush, puncture, short external contacts, or incinerate the battery
Use only the supplied power adapter to charge the battery
Incorrect use of the battery may cause a leak of chemicals or explosion The leak of chemicals may
harm the skin If any chemicals leak from the device, use a dry cloth to wipe it clean and contact
your local Philips representative for help
Dispose of used batteries according to the instructions
Electrical Fast Transients (EFT)
The system complies with the IEC 661-1-2 3rd edition standard for susceptibility to electrical fast
transients (EFT) on the power line However, if the system experiences EFT on the power line, artifacts
(vertical lines, excessive noise in image, etc) may appear on the ultrasound image To eliminate these
artifacts caused by an EFT condition, the operator should either:
Disconnect the system from the power source by unplugging the power cord from the tablet, and run
the system on its internal battery
Or
Unplug the power cord from the wall and move to a different power source that is not experiencing this
condition
Electromagnetic Interference (EMI)
Medical electrical equipment such as the system requires special precautions regarding electromagnetic
compatibility, and must be installed and put into service according to the following electromagnetic tables
All Equipment
The system is intended for use in the electromagnetic environment specified below The customer
or operator of the InnoSight Diagnostic Ultrasound System should ensure that it is used in such an
environment
On connectors labeled with the ESD sensitivity symbol , do not touch the connector pins,
and always observe the preceding ESD precautions when handling or connecting transducers
Guidance and Manufacturer’s Declaration - Electromagnetic Emissions - All Equipment
Emissions test Compliance Electromagnetic environment - Guidance
RF Emissions CISPR 11 Group 1 The InnoSight Diagnostic Ultrasound System uses RF energy
only for its internal function Therefore, its RF emissions
are very low and are not likely to cause any interference in
nearby electronic equipment