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User Manual
EMI
Although this system has been manufactured in compliance with existing EMI (Electro-Magnetic
Interference) requirements, use of this system in the presence of an electromagnetic eld can cause
momentary degradation of the ultrasound image.
If this occurs often, Samsung Medison suggests a review of the environment in which the system is
being used, to identify possible sources of electromagnetic emissions. These emissions could be from
other electrical devices used within the same room or an adjacent room. Communication devices such
as cellular phones and pagers can cause these emissions. Nearby radios, TVs, or microwave transmission
equipment can also cause interference.
CAUTION: In cases where EMI is causing disturbances, it may be necessary to relocate this system.
EMC
The testing for EMC (Electromagnetic Compatibility) of this system has been performed according to
the international standard for EMC with medical devices (IEC 60601-1-2). This IEC standard was adopted
in Europe as the European norm (EN 60601-1-2).
Guidance and Manufacturer’s Declaration - Electromagnetic Emissions
This product is intended for use in the electromagnetic environment specied below. The user is to
ensure that the product is used in the following environment.
Emission test Compliance Electromagnetic environment - guidance
RF Emission
CISPR 11
Group 1
The 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.
RF Emission
CISPR 11
Class A
The Ultrasound System is suitable for use in all establishments other
than domestic, and may be used in domestic establishments and
those directly connected to the public low-voltage power supply
network that supplies buildings used for domestic purposes,
provided the following warning is heeded:
Warning: This system is intended for use by healthcare professionals
only. This system may cause radio interference or may disrupt
the operation of nearby equipment. It may be necessary to
take mitigation measures, such as re-orienting or relocating the
Ultrasound System or shielding the location
Harmonic
Emission
IEC 61000-3-2
Class A
Flicker Emission
IEC 61000-3-3
Complies
- UGEO PT60A 1
- Safety Requirements 8
- Declarations 9
- Precautions For Use 10
- Revision History 12
- Table of Contents 13
- Chapter 3 Starting Diagnosis 14
- Chapter 6 Image Management 15
- Chapter 7 Utilities 16
- Chapter 8 Maintenance 16
- Chapter 9 Probes 17
- Chapter 1 19
- Purpose of Use 21
- Safety Information 22
- Chapter 1 Safety 23
- Electrical Safety 25
- ECG-Related Information 27
- Peripherals 29
- Mechanical Safety 35
- Biological Safety 36
- Applying ALARA 37
- Direct Controls 37
- Indirect Controls 38
- Additional Considerations 39
- Output Display Features 39
- Mechanical Index (MI) Display 40
- Thermal Index (TI) Display 40
- 2D Mode Controls 42
- Color and Power Controls 42
- Other 43
- Related Guidance Documents 44
- - (0,23 alf ) 46
- -(0,069 lf) 46
- Systematic Uncertainties 49
- Training 50
- Protecting the Environment 51
- Battery Pack 52
- Introduction 55
- Product Specications 57
- Product Conguration 59
- Touch Screen 60
- Chapter 2 Introduction 61
- Touch Panel 62
- Console 63
- Console – Left Side 64
- Console – Right Side 64
- Console - Top 64
- Console - Bottom 64
- Peripheral Devices 65
- USB Video Printer 66
- Foot Switch 66
- WLAN Card 66
- Video Out 67
- Battery Pack 69
- Battery Icons 70
- Connecting Probes 71
- UGEO PT60A CART (Optional) 72
- Accessories 73
- Optional Functions 75
- Starting Diagnosis 77
- System Power 79
- Turning the Power On 80
- Shutting Down the System 80
- Probes and Presets 81
- Selecting Probe and Preset 82
- Managing Presets 82
- Renaming Presets 83
- Deleting Presets 83
- Overwriting Presets 83
- Patient Information 84
- Gynecology 88
- Urology 88
- Vascular 88
- Abdomen 89
- Pediatric 89
- Small Parts 90
- Cardiac 90
- Anesthesia 91
- Emergency 91
- Searching Patient Information 92
- Worklist Search 93
- Diagnosis Modes 95
- Information 97
- Basic Operating Instructions 98
- Basic Mode 100
- Entering 2D Mode 101
- 2D Mode Menu 101
- Freq.(Frequency) 102
- Frame Average 102
- DR (Dynamic Range) 102
- Line Density 102
- Chapter 4 Diagnosis Modes 103
- MultiVision 104
- Biopsy Guide 105
- Needle Mate 106
- M Mode Screen 107
- M Mode Menu 108
- Color Doppler Mode 109
- C Mode Screen 110
- C Mode Menu 110
- User Manual 112
- Power Doppler Mode 113
- PD Mode Menu 114
- PW Spectral Doppler Mode 115
- Adjusting Doppler Baseline 117
- Simul. (Simultaneous) 117
- Wall Filter 117
- Combined Mode 118
- Multi-Image Mode 119
- Measurements and 121
- Calculations 121
- Measurement Accuracy 123
- Ultrasound Velocity 124
- Doppler Signal Adjustment 124
- Aliasing 124
- Calculation Equation 124
- Human Error 124
- 2D Mode 125
- M Mode 125
- Doppler Mode 125
- Color/Power Doppler Mode 126
- Cursor Position 126
- Measurement Accuracy Table 127
- Basic Measurements 128
- Deleting Measurement Results 129
- Printing Measurement Results 129
- Exiting Basic Measurement 129
- Distance measurement 130
- Angle 131
- Distance (M) 132
- Time (M) 132
- Slope 132
- Velocity 133
- Manual Trace 133
- Limited Trace 134
- Auto Trace 135
- Ellipse 136
- Trace 137
- Volume measurement 138
- Calculations by Application 139
- Common Measurement Methods 141
- Heart Rate Measurement 142
- OB Calculations 143
- Automatic Calculation 144
- AFI(Amniotic Fluid Index) 144
- Gynecology Calculations 146
- Vascular Calculations 148
- Auto IMT Measurement 149
- Viewing Reports 151
- Measurement Display Method 152
- Adding Comments 153
- Store SR 153
- Printing Reports 154
- Closing Reports 154
- Image Management 155
- Cine / Loop 157
- How to Review Images 158
- Cine Play 158
- Cine Speed 158
- Annotating Images 159
- Entering Text 160
- Text Library Menu 160
- Deleting Text 161
- Arrow Mode 161
- Entering Arrow 162
- Deleting Arrows 162
- BodyMarker 163
- Exiting Annotation 164
- Saving Images 165
- Transferring Images 166
- SonoView Mode 167
- Launching SonoView Mode 168
- Exam Mode 169
- Thumb Scroll 170
- Layouts 170
- Clip Play/Pause/Stop 170
- Searching for an Exam 170
- Selecting Image 170
- Transferring Images 171
- Print 171
- Deleting Images 172
- Exiting SonoView 172
- Utilities 173
- System Settings 175
- General System Settings 176
- Date and Time 177
- Screen Saver 177
- Common Settings 178
- Annotation Settings 179
- Measurement Settings 180
- Heart Rate 181
- Author Settings 181
- EFW Settings 182
- Peripheral Device Settings 183
- Store 184
- Brightness 184
- Clip Store 184
- Network Settings 185
- Authentication 186
- Data Encryption 186
- Password 186
- DICOM Settings 187
- DICOM Service Settings 188
- Worklist Service Server 189
- Storage Server Information 190
- Print Server Information 190
- SC Server Information 190
- PPS Server Information 190
- Storage SR Server Information 191
- Maintenance 195
- Operational Environment 197
- Product Maintenance 198
- Accuracy Checks 199
- Battery Pack Management 200
- Recharging the Battery Pack 201
- Storing the Battery Pack 203
- Disposing of the Battery Pack 203
- Information Maintenance 204
- Chapter 9 205
- Probe List 207
- Function List 209
- Thermal Index (TI) Tables 211
- Ultrasound Transmission Gel 212
- Using Sheaths 213
- Probe Safety Precautions 214
- Electric Shocks 215
- 2), 3), 6), 7) 217
- Cleaning 222
- Disinfection 223
- Biopsy Kit Components 224
- Using the Biopsy Kit 225
- Biopsy Procedure 226
- Needle Guide Alignment 227
- Assembling the Biopsy Kit 228
- Disposable adapter 229
- Biopsy Kit Specications 230
- Cleaning 231
- Disinfection 231
- Sterilization 232
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