GE Vivid S6 - Page 32

Safety
14 Vivid S5/Vivid S6 User Manual
R2424458-100 Rev. 2
• Probe Safety .................................................................................. ..... 32
• Mechanical hazards ....................................................................32
• Electrical Hazard .........................................................................33
• Biological hazards .......................................................................34
• Personnel and equipment safety ................................................ ..... 35
• Explosion hazard ........................................................................35
• Electrical hazard .........................................................................35
• Smoke and fire hazard ................................................................36
• Biological hazard ........................................................................36
• Pacemaker hazard ......................................................................36
• LCD Monitor ................................................................................37
• Electrical safety ............................................................................ ..... 39
• Internally connected peripheral devices .....................................39
• External Connection of other peripheral devices ........................39
• Allergic reactions to latex-containing medical devices ............ ..... 40
• Use of ECG .................................................................................... ..... 41
• Use of Defibrillator ....................................................................... ..... 41
• Use of Electrosurgical Unit .......................................................... ..... 41
• Electromagnetic Compatibility (EMC) ........................................ ..... 42
• EMC performance .......................................................................43
• Declaration of Emissions ............................................................44
• Declaration of Immunity ..............................................................44
• Notice upon Installation of Product .............................................44
• General notice ............................................................................45
• Peripheral Update for EC countries ............................................46
• Patient Environmental Devices ................................................... ..... 48
• Acceptable devices .....................................................................49
• Unapproved devices ...................................................................49
• Accessories, options, and supplies .............................................49
• Environmental protection ............................................................50