Operation Manual
126 Pages
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Operation Manual
Operation Manual
The MEDRAD® MRXperion MR Injection System has an expected service life* of 7 years from the date of product installation when operated according to the instructions provided with this device. These 7 years include suggested or mandatory actions of preventative maintenance and repair activities, 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 that may be required. * Expected Service Life: The length of time that an individual unit, lot, or batch of devices is expected to remain functional after it is placed into use.
Report any serious incident that has occurred in relation to this device to Bayer (radiology.bayer.com/contact) and to your local European competent authority (or, where applicable, to the appropriate regulatory authority of the country in which the incident has occurred).
A glossary of the symbols used on the MEDRAD® MRXperion MR Injection System can be found in Chapter 2 of this manual.
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1 Introduction ...1 1.1 Certifications... 1 1.2 Indications For Use ... 1 1.3 Training Information... 1 1.4 Contraindications... 1 1.5 Restricted Sales ... 1 1.6 Required Training ... 1 1.7 Disclaimers... 1
2 Symbols...3 2.1 Manufacturing Symbols ... 3 2.2 Shipper Symbols... 3 2.3 Notified Body ... 4 2.4 Regulatory Classifications... 4 2.5 MR Icons and Classifications... 6 2.6 Warning Labels and Symbols ... 6
3 Warnings, Cautions, and Notices ...9 3.1 Warnings... 9 3.2 Cautions...10 3.3 Notices...11
4 System Overview ...13 4.1 System Diagram...13 4.2 Moving the System...15 4.3 Fluid Delivery Basics ...16 4.3.1 Protocol...16 4.3.2 I Checked for Air ...17 4.3.3 Test Injection...17 4.3.4 KVO (Keep Vein Open)...17 4.3.5 Protocol Manager...17 4.3.6 Fluid Delivery System Design ...17 4.3.7 Fluid Pressure and Pressure Limiting...18 4.3.8 Response to Occlusions ...18 4.3.9 Volume and Flow Rate Protection ...18 4.4 Syringe Installation Features ...18 4.5 Basic Informatics ...19 4.6 Programming Mode...19 4.7 Using the Pedestal with Integrated IV Pole...19
5 Understanding the Display and Workstation...21 5.1 Home Screen ...21 5.2 Workstation Descriptions ...25 5.2.1 Workstation Buttons and Icons...25 5.2.2 Workstation with Pod Buttons and Icons ...27
6 Understanding the Injector Head...29 6.1 Injector Head Controls ...29
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6.2 Injector Head Components ...31 6.2.1 Manual Knobs...31
7 System Lights and Indicators...33 7.1 Injector Head Lights and Indicators ...33 7.2 Injector Status Lights...34 7.3 Workstation Power Indicators ...35 7.4 Handswitch Light ...35
8 Powering Up and Shutting Down the System ...37 8.1 Powering Up the System...37 8.2 Shutting Down the System ...38 8.2.1 Hard Shutdown...38 8.3 Restore from Injector Shutdown...38 8.4 Restore from System Shutdown...38
9 Calculators...39 9.1 Enabling Calculators ...39 9.2 Calculator Setup ...39 9.2.1 Setting Up the eGFR Calculator...40 9.2.2 Setting Up the Weight-Based Dosing Calculator...44 9.3 Using the Calculators...44 9.3.1 Using the eGFR Calculator ...45 9.3.2 Using the Weight Based Dosing Calculator ...46
10 Protocol Management ...47 10.1 Create or Edit a Protocol ...47 10.2 Save a Protocol ...50 10.3 Recall a Saved Protocol ...51
11 Preparing for Injection ...53 11.1 Control Room Preparation...53 11.1.1 Prepare Injection Protocol ...53 11.2 Scan Room Preparation ...53 11.2.1 Installing a Syringe ...55 11.2.2 Filling a Syringe: Automatically or Manually ...55 11.2.3 Attach and Prime the Tubing ...57 11.2.4 Connect the Tubing to Patient ...57
12 Arming and Injecting ...59 12.1 Add Volume Indicator ...59 12.2 Arming the Injector...59 12.2.1 Arming from the Control Room ...59 12.2.2 Arming from the Scan Room ...61 12.2.3 Starting KVO (Optional)...62 12.3 Initiating an Injection ...62 12.4 Operator Initiated Hold ...63
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12.5 Aborting an Injection ...63 12.6 Viewing Injection Progress...63 12.7 Reminders ...64
13 Completing an Injection ...65 13.1 Injection Complete ...65 13.2 Injection Aborted...66 13.3 Exiting Injection Complete ...67 13.3.1 Conducting Another Injection ...67
14 Removing Disposable Syringes and Connector Tube ...69 14.1 Removing Disposable Syringes and Connector Tube...69
15 Advanced Configurations ...71 15.1 System Setup ...71 15.1.1 System Setup Configurable Items ...72 15.2 Calculator Setup...72 15.3 Protocol Manager Setup...73 15.3.1 Delete a Protocol...73 15.3.2 Rearrange Protocol List ...74 15.3.3 Move Protocol to a New Region...74 15.3.4 Hide/Show a Region ...74 15.3.5 Rename a Region...75 15.4 Fluid Delivery Setup...75 15.4.1 Fluid Delivery Setup Configurable Items ...77 15.4.2 Contrast Type Setup ...77 15.5 Help ...80 15.5.1 Accessing the Help System...80 15.6 Fluid A ...81
16 System Messages...83 16.1 Type 1 Messages...83 16.2 Type 2 Messages...83 16.3 Type 3 Messages...84
17 Cleaning and Maintenance...85 17.1 In the Case of Saline or Contrast Media Spills...86 17.1.1 Cleaning the Injector Head ...86 17.2 Daily and In the Case of Visible Contamination...87 17.2.1 Cleaning the Injector Head ...87 17.2.2 Disinfecting the Injector Head ...88 17.3 Daily ...89 17.3.1 Inspecting the Injector Head and Mounting ...89 17.3.2 Cleaning and Disinfecting the injector Head ...89 17.3.3 Cleaning the Pistons and Syringe Interface...90 17.3.4 Cleaning the Pedestal and Base ...92 17.3.5 Cleaning the Workstation Screen ...93 17.4 Monthly ...94
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17.4.1 Operational Checkout...94 17.5 Annually ...95 17.5.1 Injection System Calibration ...95 17.5.2 Checking Electrical Leakage ...95
18 Specifications...97 18.1 Workstation Specifications ...97 18.1.1 Workstation Dimensions ...97 18.1.2 Workstation Connections ...98 18.1.3 Workstation Input Power Requirements ...98 18.2 Workstation with Pod Specifications ...99 18.2.1 Workstation with Pod Dimensions and Weight...99 18.2.2 Workstation with Pod, Pod Connections ...99 18.2.3 Workstation with Pod, Display Connections ... 100 18.2.4 Workstation with Pod Input Power Requirements... 100 18.3 Injector (Scan Room Unit) Specifications... 101 18.3.1 Injector (Scan Room Unit) Dimensions ... 101 18.3.2 Scan Room Unit Power Supply Dimensions... 102 18.3.3 Input Power Requirements... 102 18.4 Environmental Specifications ... 102 18.4.1 Non-Operating (Transportation and Storage)... 102 18.4.2 Operating ... 102 18.4.3 Protection Against Electrical Shock ... 103 18.4.4 EMI/RFI ... 103 18.4.5 Protection Against the Ingress of Fluids... 103 18.4.6 Mode of Operation ... 103 18.5 System Capabilities ... 104 18.6 Approximate Heat Generation... 104 18.7 Over and Under Infusion Protection ... 104 18.8 Fluid Delivery Performance ... 105 18.9 System Fluid Performance ... 105 18.9.1 Factors Affecting Flow Rates ... 105 18.9.2 Maximum Flow Rate Performance... 106 18.10 Forward and Reverse Controls ... 106 18.11 Power Cable Specifications... 106 18.12 Ground Continuity... 106 18.13 Classifications ... 107 18.14 MEDRAD® MRXperion MR Injection System Cybersecurity and IT Network Connection... 107 18.14.1 System Cybersecurity Protection... 107 18.14.2 Certegra® Workstation Cybersecurity... 107 18.14.3 IT Network Connection ... 107
19 Options and Accessories ...109 19.1 MEDRAD® MRXperion MR Injection System... 109 19.2 MEDRAD® MRXperion MR Injection System Syringe Kits... 109 19.3 Handswitch... 109 19.4 IV Poles... 109 19.5 Manuals... 110 19.6 Penetration Panel Filter Kit... 110 19.7 Mobile Mount Kit ... 110
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19.8 Scan Room DC Power Cables... 110 19.9 Prefilled Syringe Adapters (PFA) ... 110
20 Compliance to IEC 60601-1-2 / 2nd, 3rd, and 4th Editions ...111
Operation Manual
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Introduction
This manual applies to the MEDRAD® MRXperion MR Injection System, referred to as the system throughout this document, Catalog Number: MRXP 200. Read all of the information contained in this manual. Understanding this information will assist users in operating the system in a safe manner. NOTE: Operating specifications, options, accessories, and feature availability may vary by country. Check with a local product representative for Bayer and refer to country-specific operating instructions. Refer to the MEDRAD® MRXperion Prefilled Syringe Adapter operation manual for more information regarding the use of the system with prefilled syringe adapters (PFAs).
1.1 Certifications This device is equipped to operate at 100-240 VAC, 50/60 Hz and is designed to comply with IEC 60601-1 (2nd and 3rd Edition Amendment 1) and IEC 60601-1-2 (2nd, 3rd, and 4th Edition) standards, including national differences. Special precautions regarding ElectroMagnetic Compatibility (EMC) are required for installation and use of this injection system. Detailed EMC information can be found in "Chapter 20 - Compliance to IEC 60601-1-2 / 2nd, 3rd, and 4th Editions".
1.2 Indications For Use The MEDRAD® MRXperion MR Injection System is a syringe-based fluid delivery system indicated for delivery of contrast media and saline during MR procedures. It is intended to be used for the specific purpose of injecting intravenous MR contrast media and saline into the human vascular system for diagnostic studies in magnetic resonance imaging (MRI) applications with MRI scanners that have a magnetic field strength between 0.7 Tesla and 3.0 Tesla. Only trained healthcare professionals are intended to operate this device.
1.3 Training Information This manual is intended as an extension of the user interface of the MEDRAD® MRXperion MR Injection System to provide procedural and technical information. Additional MEDRAD® MRXperion training information will be available in the following formats: Q
On-site initial installation and additional training as requested
Q
MEDRAD® MRXperion Quick Guides
Q
Syringe instructions for use (IFU)
Please contact Bayer or your local representative for Bayer if any of these resources are needed.
1.4 Contraindications None known.
1.5 Restricted Sales Federal (USA) Law restricts this device to sale by or on the order of a physician.
1.6 Required Training The device is intended to be used by trained personnel with experience in magnetic resonance (MR) imaging diagnostic studies.
1.7 Disclaimers External wiring and modifications disclaimers: Bayer disclaims liability for any modifications or interfaces with other equipment that are not in conformity with the specifications and information contained within this manual. Anyone who connects additional equipment to the device or configures a medical system is responsible that the system complies with the relevant requirements of IEC 60601-1. An accessory or equipment connected to the device must be
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certified to either IEC 60601-1 (Operator or Patient Environment Use) or, outside the patient environment, the level of safety must be equivalent to equipment complying with their respective IEC or ISO safety standards, e.g. IEC 62368-1 or IEC 609501 (Operator Environment Use Only), and must comply with the relevant requirements according to IEC 60601-1. Consult Bayer for any modifications to the equipment. The system is not intended to deliver contrast agents and/or saline to more than one patient from the same saline container and Bayer disclaims any and all liability or consequences resulting from use of the same container on more than one patient. Use of syringes and other disposables from a source that is not approved by Bayer may cause injury as set forth herein and such use may also void the warranty associated with this product. The MEDRAD® MRXperion MR Injection System is not intended for portable use. Screen images in this manual are for illustration purposes only. Actual screens may vary.
Operation Manual
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2-3
Symbols Q
"Manufacturing Symbols"
Q
"Shipper Symbols"
Q
"Notified Body"
Q
"Regulatory Classifications"
Q
"MR Icons and Classifications"
Q
"Warning Labels and Symbols"
2.1 Manufacturing Symbols
Manufacturer (ISO 15223-1, 5.1.1)
Authorized representative in the European community (ISO 15223-1, 5.1.2)
Date of Manufacture (ISO 15223-1, 5.1.3)
2.2 Shipper Symbols
Temperature range (ISO 15223-1, 5.3.7)
Humidity range (ISO 15223-1, 5.3.8)
Atmospheric pressure range (ISO 15223-1, 5.3.9)
Serial number (ISO 15223-1, 5.1.7)
Catalog number (ISO 15223-1, 5.1.6)
This side up (ISO 7000, 0623)
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MEDRAD® MRXperion
Keep dry (ISO 15223-1, 5.3.4)
Fragile, handle with care (ISO 15223-1, 5.3.1)
PN
Part Number
Net Weight (ISO 7000, 1321B)
Quantity (IEC TR 60878, 2794)
2.3 Notified Body Indicates that this device conforms to the requirements of the European Union Medical Device Regulation 2017/745
2.4 Regulatory Classifications Identifies a type BF applied part complying with IEC 60601-1 standards (IEC 60417, 5333) Medical - General Medical Equipment As To Electrical Shock, Fire, and Mechanical Hazards Only In accordance with ANSI/AAMI ES60601-1 (2005) + AMD 1 (2012) CAN/CSA-C22.2 No. 60601-1 (2014) See accompanying documentation. This symbol indicates the user shall refer to the instructions-for-use to ensure safe operation. (ISO 7010, M002)
CLASS 1
Indicates the injection system is Class 1 medical equipment as defined by IEC 606011 standards for protection from electric shock
Class II Equipment, Double Insulated. (IEC 60417, 5172)
IPX0 Code that indicates non-protection against ingress of water (IEC 60529)
IPX1 Code that specifies the degree of protection provided by the enclosure against vertically falling water drops (IEC 60529)
Operation Manual
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Indicates separate collection for Electrical and Electronic Equipment per Directive 2002/96/EC. Refer to the following website for additional information: www.weee.bayer.com
Indicates that this product contains certain toxic or hazardous substances or elements and can be used safely during its environmental protection use period, indicated by the number in the center of the logo. This product should be recycled immediately after its environmental protection use period has expired. Identifies the Equipotential connection. The Equipotential Connector (EPC) is an electrically bonded terminal on the injector that is used as a connection point between other medical electrical equipment. The EPC's function is to minimize any voltage potentials differences between all connected equipment. The EPC is not designed to be an electrical safety ground. (IEC 60417, 5021)
Does not contain serviceable parts.
Indicates that a component contains an electrical fuse that can be replaced. (IEC TR 60878, 5016)
Alternating Current (IEC 60417, 5032)
Identifies power switch for equipment. (IEC TR 60878, 5009)
Identifies a computer network connection. (IEC TR 60878, 5988)
Identifies a power supply connection. (IEC TR 60878, 5534)
Identifies a terminal suitable for direct current. (IEC TR 60878, 5031)
Identifies a transfer of displayed image to a second screen. (IEC TR 60878, 5892)
Identifies a hand-held switch connection. (IEC TR 60878, 5322)
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MEDRAD® MRXperion
Identifies an input terminal. (IEC TR 60878, 5034)
Identifies an output terminal. (IEC TR 60878, 5034)
Identifies service assistance. (IEC TR 60878, 0717)
2.5 MR Icons and Classifications
MR
MR Conditional
Has been demonstrated to pose no known hazards in a specified MR environment with specified conditions of use as defined by the ASTM International Standards for MRI Device Marking. (IEC 62570, 7.3.2)
MR Unsafe
Known threat or poses a hazard in all MR environments as defined by the ASTM International Standards for MRI Device Marking. (IEC 62570, 7.3.3)
2.6 Warning Labels and Symbols Pushing prohibited in this area. Do not push the injector above this label. (ISO 7010, P017)
Do not coil the cable to the Power Supply on or near the injector or magnet. Excess cable should be tie wrapped in a figure-eight configuration and positioned as far away from the magnet as possible. Looped or coiled cable could create image artifacts.
Caster brakes must be used to prevent the injection system from drifting during use.
The injector (scan room unit) power supply must be more than 6ft (1.8m) away from the magnet.
The optional Penetration Panel Filter must be more than 6ft (1.8m) away from the magnet.
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Caution:
Transportable Weight- 43.4kg
Safe Working Load- 0.75kg
Warning: Refer to warnings and cautions on Instructions for Use packaged in each carton. (ISO 7010, W001) Attention: Refer to warnings and cautions on Instructions for Use packaged in each carton. (ISO 15223-1, 5.4.4)
Warning: Indicates hazardous voltage. (ISO 7010, W012)
Consult instructions for use (ISO 15223-1, 5.4.3)
WARNING
Indicates that the information is a warning. Warnings advise you of circumstances that could result in injury or death to the patient or operator. Read and understand the warnings before operating the injection system.
CAUTION
Indicates that the information is a caution. Cautions advise you of circumstances that could result in minor or moderate injury to the patient or operator. Read and understand the cautions before operating the injection system.
NOTICE
Indicates that the information is a notice. Notices advise you of circumstances that could result in damage to the device. Read and understand the notices before operating the injection system.
Note
Indicates that the information that follows is important information or a tip related to the proper functionality of the system that will help the operator to recover from an error or point to related information within the manual. Read and understand the notes before operating the system.
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Warnings, Cautions, and Notices Q
"Warnings"
Q
"Cautions"
Q
"Notices"
3.1 Warnings WARNINGS Air Embolism Hazard - Serious patient injury or death may result. Q
Use only disposables supplied by Bayer. Refer to "Section 19.2 - MEDRAD® MRXperion MR Injection System Syringe Kits".
Q
Use only catheters and connectors with pressure ratings that are compatible with this system. Refer to "Section 18.9.2 - Maximum Flow Rate Performance" and "Section 18.5 - System Capabilities" for programmable pressure limit options.
Q
Use only accessories and options approved by Bayer.
Q
The operator needs to check for air to confirm that the syringes and tubing have been inspected for the presence of air.
Environmental Contamination Hazard - Serious patient or worker injury or death may result. Q
Visually inspect all components before use.
Q
Do not use damaged components.
Electric Shock Hazard - Serious patient and/or worker injury or death may result. Q
Only use the power cord supplied with the system or by the Bayer representative.
Q
Equipment must only be connected to a supply mains with protective earth.
Q
Do not remove or open any enclosure, as hazardous voltages exist within system components.
Q
Do not immerse any system components in water or cleaning solutions.
Q
Disconnect the system from supply mains before cleaning.
Q
Do not use the system if any worn or damaged cabling is detected. Contact Bayer for replacement.
Fire Hazard - Serious patient and/or worker injury or death may result. Q
Use the correct fuse type, replaced by Bayer or personnel trained by Bayer.
Explosion Hazard - Serious patient and/or worker injury or death may result. Q
The system contains a lithium ion battery pack. Replacement and disposal shall be performed only by a qualified service engineer. Please contact Bayer for assistance.
Compromised Efficacy Hazard - Serious patient injury or death may result. Q
Do not use this system to deliver any fluid other than intravenous MR contrast media and saline.
Q
Do not retract pistons with connector tube installed.
Procedure Delay Hazard - Serious patient and/or worker injury or death may result. Q
Turn off any other equipment that could generate high electromagnetic fields or high-level electrostatic discharge.
Personal injury or equipment damage may result when standing on the Power Supply Enclosure. Q
Do not stand on the power supply enclosure.
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MEDRAD® MRXperion
WARNINGS Patient and/or worker injury or equipment damage may result. Q
The workstation (control room unit) is MR unsafe and is not for use in the scan room. The workstation is a known threat or poses a hazard in all MR environments as defined by the ASTM International Standards for MRI Device Marketing.
Q
The Injector (scan room unit) and power supply are MR conditional. The scan room unit and power supply have been demonstrated to pose no known hazards in a specific MR environment with specified conditions of use as defined by the ASTM International Standards for MRI Device Marketing.
Q
Do not make any unauthorized modifications to the injector or any of its parts.
Mechanical Hazard - Serious patient injury could result from fluid leaks or tubing ruptures during an injection. Q
Use only disposables or accessories supplied by Bayer. Refer to "Chapter 19 - Options and Accessories" for more information.
Q
Use only syringes and tubing with a pressure rating greater than the maximum programmable pressure limit of the injection system, which is 325 psi (2241 kPa).
Q
Ensure that the fluid path is open and do not use syringes and tubing rated below 350psi (2410 kPa). An occlusion in the fluid path and/or use of syringes or tubing rated below 350 psi (2410 kPa) may result in leaks or ruptures.
Q
Use catheters with pressure ratings compatible with this system. Refer to "Section 18.9.2 - Maximum Flow Rate Performance" and "Section 18.5 - System Capabilities" for programmable pressure limit options.
Q
Patient injury and/or catheter damage may result from using tubing set that is too short. Operator must consider tubing length and stretch limitations when moving the injector or the patient.
3.2 Cautions
CAUTIONS Mechanical Hazard - Minor or moderate patient and/or worker injury may result. Q
Only use the system as defined in this manual. Follow the instructions given in system communication or fault messages.
Q
Do not use the system in the presence of flammable (such as anesthetics) or combustible gases or other agents.
Q
Use only non-magnetic tools to install any scanner/magnet room components.
Q
Dispose of system components and accessories according to local regulations or contact Bayer.
Q
When moving the system, hold the pedestal no higher than 45inches (114.3 cm) above the floor.
Electric Shock Hazard - Minor or moderate patient and/or worker injury may result. Q
Only plug the system into a direct mains access point.
Q
Make sure the direct mains access point is accessible during operation of the system.
Q
Do not plug the system power cords into an extension cord or multi-outlet power strip.
Q
Verify that the voltage and frequency as labeled matches the voltage and frequency of the electrical outlet.
Q
Use only Bayer-approved accessories.
Do not adjust or transport the system with fluid containers attached. Minor or moderate patient and/or worker injury may result. Q
The fluid containers and/or holder may fall, causing patient injury and/or property damage.
Q
Attach containers only after the system is in a stationary position.
Operation Manual
3.3 Notices NOTICE Electro-Mechanical Hazard - Equipment Damage may result. Q
Do not use the system immediately after it has been brought indoors from extreme outside temperatures.
Q
Allow the system to stabilize at room temperature before use.
Q
Condensation may cause electrical damage to the injection system.
Mechanical Hazard - Equipment Damage may result. Q
Do not touch the display screen with a sharp object.
Q
Component damage may occur if not installed properly. Ensure all connections are secure; do not over-tighten. This will help minimize leaks, disconnection, and component damage.
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System Overview Q
"System Diagram"
Q
"Moving the System"
Q
"Fluid Delivery Basics"
Q
"Syringe Installation Features"
Q
"Basic Informatics"
Q
"Programming Mode"
Q
"Using the Pedestal with Integrated IV Pole"
WARNING Patient and/or worker injury or equipment damage may result. Q
The workstation (control room unit) is MR unsafe and is not for use in the scan room. The workstation is a known threat or poses a hazard in all MR environments as defined by the ASTM International Standards for MRI Device Marketing.
Q
The Injector (scan room unit) and power supply are MR conditional. The scan room unit and power supply have been demonstrated to pose no known hazards in a specific MR environment with specified conditions of use as defined by the ASTM International Standards for MRI Device Marketing.
Q
Do not make any unauthorized modifications to the injector or any of its parts.
4.1 System Diagram The system is comprised of a scan room unit (injector) and a control room unit (workstation). These components are connected by a fiber optic communications link. NOTE: When using the system with an open-bore scanner, it is recommended that the injector be placed a minimum of 60 inches (152.4 cm) from the facade of the scanner. NOTE: When using the system with a Siemens MAGNETOM 1.5T or 3.0T scanner, it is recommended that the injector be placed a minimum of 18 inches (45.72 cm) from the facade of the scanner. NOTE: Consider limits on the length of the connector tubing and patient position when placing the injector. NOTE: Do not place the scan room unit in a magnetic field greater than 1000G without the casters being locked.
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MEDRAD® MRXperion
1
3
5
2
4
6
9
8
7
Figure 4 - 1: System Diagram - Power Supply in Scanner Room Scan Room
Control Room
1 - Scan Room Unit (Injector)
6 - Control Room Unit (Workstation)
2 - Power Cable
7 - Workstation Power Supply
3 - Scan Room Unit Power Supply
8 - Fiber Optic Communication Link
4 - Fiber Optic Communication Link
9 - VirtualCare™/Network Cable
5- Fiber Optic Quick Disconnect
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6
5
11 4 1
2
7
3
10
12
9
8
Figure 4 - 2: System Diagram - Power Supply Outside Scanner Room Scan Room
Control Room and MRI Equipment Room
1 - Scan Room Unit (Injector)
6 - Penetration Panel Filter
2 - Power Cable
7 - Scan Room Unit Power Supply
3 - Fiber Optic Communication Link
8 - Workstation Power Supply
4 - Fiber Optic Quick Disconnect
9 - Fiber Optic Communication link
5 - Penetration Panel
10 - Control Room Unit (Workstation) 11 - DC Power Cable 12 - VirtualCare™/Network Cable
4.2 Moving the System WARNING Patient injury could result from movement of the scan room unit (injector) after the patient is connected to the fluid path. Q
Do not move the injector with the patient connected.
Q
Lock the casters at the base of the unit to prevent unintended movement.