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THE SYSTEM REQUIRES SPECIAL PRECAUTIONS REGARDING EMC

. Install and put into service according to the EMC 

information provided below:

Guidance and manufacturer's declaration - electromagnetic emissions

The system is intended for use in the electromagnetic environment specified below. The customer or user of the system should assure that it is used in such 
an environment.

Emissions test

Compliance

Electromagnetic environment - guidance

RF emissions
CISPR 11 

Group 1

The 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 emissions
CISPR 11

Class A

The emission characteristics of this system make it suitable for use in 
industrial areas and hospitals (CISPR 11 Class A). If the system is 
used in a residential environment (for which CISPR 11 Class B is 
normally required), this equipment might not offer adequate 
protection to radio-frequency communication services. The user 
might need to take mitigation measures, such as relocating or 
reorienting the equipment.

Harmonic emissions
IEC 61000-3-2

Not applicable

Voltage fluctuations / flicker emissions
IEC 61000-3-3

Not applicable

Guidance and manufacturer's declaration - electromagnetic immunity

The system is intended for use in the electromagnetic environment specified below. The customer or user of the system should assure that it is used in such 
an environment.

Immunity test

IEC 60601 Test Compliance Level

Electromagnetic environment - guidance

Electrostatic discharge 
(ESD)
IEC 61000-4-2 

±8 kV contact
±2, ±4, ±8, ±15 kV air

Floors should be wood, concrete or ceramic tile. If floors are 
covered with a synthetic material, the relative humidity 
should be at least 30%.

Electrical fast transient/
burst
IEC 61000-4-4 

±2 kV for a.c. mains
±1 kV for I/O ports

Mains power quality should be that of a typical commercial or 
hospital environment.

Surge
IEC 61000-4-5 

± -0.5 kV, ± -1 kV, ± -2 kV line to ground
± -0.5 kV, ± -1 kV line to line

Mains power quality should be that of a typical commercial or 
hospital environment.

Voltage dips
IEC 61000-4-11 

100% Vac for 0.5 cycles at 0°, 45°, 90°,135°,180°, 225°, 
270°, 315

Mains power quality should be that of a typical commercial or 
hospital environment. If the user of the system requires 
continuous operation during power mains interruptions, it is 
recommended the system be powered from an 
uninterruptible power supply or battery.

100% Vac for 1.0 cycles at 0°

30% Vac for 30 cycles at 0°

100% Vac for 250 (50Hz) cycles or 300 (60Hz) cycles at 0°

Voltage interruptions
IEC 61000-4-11

0% a.c. 250(50 Hz) or 300(60 Hz) at 0°

Power frequency
(50/60 Hz) magnetic field
IEC 61000-4-8 

30 A/m

Power frequency magnetic fields should be at levels 
characteristic of a typical location in a typical commercial or 
hospital environment.

Summary of Contents for MEDRAD SCT 110

Page 1: ...CT Injection System CT Injection System Operation and Installation Manual MEDRAD Stellant Imaging System Interface ISI 700 Module...

Page 2: ......

Page 3: ...as well as required calibration s that are needed Required reading includes the instructions for use and other materials provided with the device This also includes any hardware and software updates...

Page 4: ...MEDRAD Stellant ISI700ModuleOperationandInstallationManual ii...

Page 5: ...nstallation 6 Operational Checkout 8 Configuration 9 Overview of Operation 9 Injector Head Indicator Lights 10 Details of Operation 10 Hold and Test Inject features 10 Scan Delay 11 ISI Module Cables...

Page 6: ...MEDRAD Stellant ISI 700 Module Operation and Installation Manual iv...

Page 7: ...f allowing an injector to interface with a CT scanner Contraindications The ISI module is not to be used for any other use for which the device is not indicated This device is not to be used for drug...

Page 8: ...mains the same Throughout the manual Display and Control Unit DCU and Certegra Workstation will be used to refer to the two when there are differences in how information is presented on the screens Sy...

Page 9: ...in each carton ISO 15223 1 5 4 4 Warning Indicates hazardous voltages ISO 7010 W012 Indicates alternating current IEC 60417 5032 Indicates scanner connection Identifies a terminal suitable for direct...

Page 10: ...communicating to the ISI module The scanner signals are in a state that will allow arming the injector The user is not able to arm the injector The injector is configured for ISI and it is communicat...

Page 11: ...use it to fail Installation must be completed by properly trained personnel Contact your scanner manufacturer for configuration and installation assistance Patient injury could result from using impro...

Page 12: ...a soft cloth or paper towel dampened with cleaning solution Do not use strong cleaning agents and solvents Warm water and a mild disinfectant are all that are required to clean the injector Do not use...

Page 13: ...Connect the power cable to the ISI module Ensure power indicator is illuminated 5 If a Certegra Workstation is being installed as an upgrade to an existing injector with an ISI 700 option determine w...

Page 14: ...Operational Checkout A basic functional checkout of the ISI module should be included as part of regular maintenance Verifying proper operation of the ISI module will help in detection of any problems...

Page 15: ...itiation The ISI module supports the following two methods 1 By pressing the injector start switch the injector notifies the scanner that it can begin the scanning sequence 2 The scanner initiates the...

Page 16: ...d with a short flash long flash pattern Details of Operation 1 Program the scanner You will see the ISI Ready icon when the scanner is ready 2 Program the injector 3 Arm the injector NOTE For specific...

Page 17: ...injector screen Text Box Message What it means Actions to be taken Display and Control Unit DCU Scanner not ready Certegra Workstation Imaging system not ready When the ISI module is configured On or...

Page 18: ...ntact Bayer for further support Schematic Diagram Note Maximum rating for scanner relay contacts 0 75 A 30 VDC Minimum rating for scanner relay contacts 10 a 10mV Display and Control Unit DCU ISI modu...

Page 19: ...at any time by disarming it This signal would immediately stop the injection of contrast If the injector is armed this signal would be high making this signal go to zero disarms the injector 25 Note...

Page 20: ...for a Class 1 Medical Device EMI RFI The injection system is classified as Group 1 Class A equipment per the requirements of IEC 60601 1 2 Accessories provided by Bayer will also comply with this sta...

Page 21: ...Mode of Operation Per IEC 60601 1 the mode of operation for the ISI module is continuous It is capable of operation under normal load for an unlimited period without excessive temperature being develo...

Page 22: ...MEDRAD Stellant ISI700ModuleOperationandInstallationManual 16...

Page 23: ...ing and measurement techniques Surge immunity test IEC 61000 4 6 Electromagnetic compatibility EMC Part 4 6 Testing and measurement techniques Immunity to conducted disturbances induced by radio frequ...

Page 24: ...rence by maintaining a minimum distance between portable and mobile RF communications equipment transmitters and the system as recommended below according to the maximum output power of the communicat...

Page 25: ...use in the electromagnetic environment specified below The customer or user of the system should assure that it is used in such an environment Immunity test IEC 60601 Test Compliance Level Electromag...

Page 26: ...d with the following symbol Non ionizing Radiation Symbol IEC TR 60878 5140 NOTE 1 At 80 MHz and 800 MHz the higher frequency range applies NOTE 2 These guidelines may not apply in all situations Elec...

Page 27: ...ctor Head Indicator Lights 10 Installation 6 J L J1 Pins 13 M O Maintenance 11 Messages and Descriptions 11 Operation Details of 10 Operation Overview 9 Operational Checkout 8 P R Rating maximum 12 Ra...

Page 28: ...MEDRAD Stellant ISI700ModuleOperationandInstallationManual 22...

Page 29: ......

Page 30: ...in this publication at any time without prior notice or obligation Please contact your authorized Bayer representative for the most current information All patient data that appear in this document ar...

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