x Operator’s Manual
Contents
B Wireless LAN ..................................................................................................... B - 1
B.1 Use the Wireless Feature .............................................................................................. B - 2
B.2 IP Configure ................................................................................................................. B - 2
B.3 EAP Network ................................................................................................................B - 3
C iScanHelper ........................................................................................................ C - 1
C.1 Use iScanHelper for Reference .................................................................................... C - 1
C.2 Use iScanHelper for Learning or Training ................................................................... C - 1
C.3 Basic Screen and Operation .......................................................................................... C - 2
D iVision ................................................................................................................. D - 1
D.1 Demonstration Item ...................................................................................................... D - 1
D.2 Demonstration Catalog ................................................................................................. D - 1
D.2.1 Demo Catalog ....................................................................................................D - 1
D.2.2 Customize Catalog .............................................................................................D - 1
D.3 Copy the File ................................................................................................................ D - 2
D.4 Demonstration Mode ....................................................................................................D - 2
D.5 Option of Demo ............................................................................................................D - 2
E Acoustic Output ................................................................................................. E - 1
E.1 Concerns with Bioeffects ...............................................................................................E - 1
E.2 Prudent Use Statement ...................................................................................................E - 1
E.3 ALARA Principle (As Low As Reasonably Achievable) .............................................E - 1
E.4 MI/TI Explanation .........................................................................................................E - 2
E.4.1 Basic Knowledge of MI and TI ...........................................................................E - 2
E.4.2 MI/TI Display ......................................................................................................E - 3
E.5 Acoustic Power Setting ..................................................................................................E - 3
E.6 Acoustic Power Control .................................................................................................E - 4
E.7 Acoustic Output .............................................................................................................E - 4
E.7.1 Derated Ultrasonic Output Parameters ................................................................E - 4
E.7.2 Limits of Acoustic Output ...................................................................................E - 5
E.7.3 Differences between Actual and Displayed MI and TI .......................................E - 5
E.8 Measurement Uncertainty ..............................................................................................E - 6
E.9 References for Acoustic Power and Safety ....................................................................E - 6
F Electrical Safety Inspection ...............................................................................F - 1
F.1 Power Cord Plug ............................................................................................................F - 1
F.2 Device Enclosure and Accessories ................................................................................F - 2
F.2.1 Visual Inspection .................................................................................................F - 2
F.2.2 Contextual Inspection ..........................................................................................F - 2
F.3 Device Labeling .............................................................................................................F - 2
F.4 Protective Earth Resistance ............................................................................................F - 2
F.5 Earth Leakage Test .........................................................................................................F - 2
F.6 Enclosure Leakage Test .................................................................................................F - 3
F.7 Patient Leakage Current .................................................................................................F - 3
F.8 Mains on Applied Part Leakage .....................................................................................F - 4
F.9 Patient Auxiliary Current ...............................................................................................F - 4
G EMC Guidance and Manufacturer’s Declaration ......................................... G - 1