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Regulatory Requirement

This product complies with regulatory requirements of the

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following European directive 93/42/EEC concerning medical

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devices.

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Some options are not available insome model!!

P/N 4701-0061-01A BASIC Operator’s Manual
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SSI-6000/SSI-5800 /SSI-5500/SSI-5500BW™
Diagnostic Ultrasound System

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1 SYSTEM SAFETY AND MAINTENANCE ...........................................1-1
1.1. Safety Overview......................................................................................1-1
1.2. WARNING Symbols ................................................................................1-3
1.3. Biological Safety......................................................................................1-4
1.4. Scanning Patients and Education ...........................................................1-5
1.4.1 Safe ScanningGuideline.....................................................................1-6
1.4.2 Understanding the MI/TI Display .........................................................1-8
1.5. Environmental Requirements ................................................................1-13
1.6. Transport and Storage Environmental Requirements ...........................1-14
1.7. Electrical Requirements........................................................................1-14
1.8. Electrical Safety.....................................................................................1-15
1.9. Transducer Maintenance.......................................................................1-16
1.10. System Positioning/Transporting...........................................................1-22
1.10.1 Movingthe System ........................................................................1-22
1.10.2 Transporting the System................................................................1-23
2 SYSTEM SPECIFICATIONS ...............................................................2-1
2.1. Base System ...........................................................................................2-12.2. Application and Contraindication.............................................................2-7
2.3. Image Modes...........................................................................................2-7
2.4. User Interface Control .............................................................................2-8
2.5. Probes andAccessories..........................................................................2-9
2.6. Physical Specifications.......................................................................... 2-11
2.7. User Interface Function Keys Description............................................. 2-11
2.7.1 System power up...............................................................................2-12
2.7.2 EXAM-Key.........................................................................................2-12
2.7.3 Mode Select Key (M, B, THI, CFM, DPI, TDI, PW, CW) ...................2-12
2.7.4 PATIENT Key / Patient Data Entry window .......................................2-16
2.7.5 System Set-Up ..................................................................................2-19
2.7.6 Save Key...........................................................................................2-24
2.7.7 M-Tuning Key ....................................................................................2-25
2.7.8 4D Key...............................................................................................2-25
2.7.9 Video Print Key..................................................................................2-25
2.7.10 PRINT...