Operation Manual
Table Of Contents
- 1. Quick Start
- 2. Introduction
- 3. Getting Started
- 3.1. Installation
- 3.2. Injector Features
- 3.3. Symbols
- 3.3.1. Symbols used in this manual
- 3.3.2. Symbols used on labelling
- 3.3.3. Handswitch and Footswitch
- 3.3.4. Icons and Buttons used on the Injector Touch Screen Graphical Interface
- 3.3.5. Injector Buttons
- 3.3.6. Remote Control Symbols and Buttons
- 3.3.7. Injector Visual Indicators
- 3.3.8. Icons and Buttons used on the RCU Touch Screen Graphical Interface
- 4. Clinical Information
- 5. Operation Description
- 5.1. Turning the System On for the First Time
- 5.2. Syringe, Quick Fill Tube, Fill Spike, and Connector Tubes
- 5.3. Filling a Syringe Using a Quick Fill Tube (QFT) or Fill Spike on the Injector
- 5.4. [Optional] Off-line Filling
- 5.5. Connector Tube Installation
- 5.6. Dismounting a Syringe
- 5.7. Performing an injection
- 5.8. Programming
- 5.9. Options Menu
- 5.10. [RCU models] Operation Description with Remote Control Unit
- 5.10.1. RCU Features–
- 5.10.2. The Injector and the RCU
- 5.10.3. Turning the System On / Off
- 5.10.4. Injector Controller Application
- 5.10.5. Filling State
- 5.10.6. Routine Protocol
- 5.10.7. Arming
- 5.10.8. Check for Air
- 5.10.9. Starting the Injection
- 5.10.10. Injection in Progress
- 5.10.11. Injection Control Buttons
- 5.10.12. Injection Review
- 5.10.13. Protocol Edit
- 5.10.14. Edit Lock
- 5.10.15. Parameter Value Edit
- 5.10.16. Injecting remaining volume
- 5.10.17. Edit Phase Type
- 5.10.18. Open Protocol
- 5.10.19. Protocol Save
- 5.10.20. Common Injecting Alarms / Warnings
- 5.10.21. RCU Manager
- 5.10.22. RCU Setup
- 5.10.23. History Viewer
- 5.10.24. Protocol Manager
- 5.10.25. eGFR (glomerular filtration rate) Calculator
- 5.11. [Optional] DC200 Scanner Interface
- 5.12. [Optional] Protocol Assistance Tool (PAT)
- 6. Cleaning and Maintenance
- 7. Trouble-shooting
- 8. Specifications
- 8.1. Dimensions
- 8.2. Mechanical
- 8.3. Functional
- 8.4. Controls
- 8.5. Environmental
- 8.6. Electrical
- 8.7. Connectors
- 8.8. IEC 60601-1 Classifications
- 8.9. Ground Continuity
- 8.10. RoHS Statement
- 8.11. IEC60601-1-2:2014 (4th Ed) Compliance
- 8.12. Models
- 8.13. Accessories
- 8.14. Manufacturer’s Software License Information
- 8.15. FCC Statement
- 9. Index
MEDRAD
®
Salient Operation Manual 3
2. Introduction
Thank you for purchasing the MEDRAD
®
Salient Contrast Injector. Read this manual and follow the safety
precautions closely so you will be able to use the injector and all of its features properly and safely. For the latest
support information, visit our website: http://www.imaxeon.com/
Record the model number in the table below, together with the serial number of your system and your
IMAXEON representative’s telephone number.
DC009S (Single)
DC009D (Dual)
DC009SW (Single with Wireless RCU)
DC009DW (Dual with Wireless RCU)
Model No Serial No: IMAXEON Service Representative Tel No:
2.1. Important Safety Notice
The information in this manual is intended for medical personnel with adequate training and experience in X-ray
imaging studies. Any attempt to operate or repair a medical device such as the injector without adequate training
may result in personal injury, property damage or patient injury.
2.2. How To Read This Manual
READ this manual thoroughly before operating the injector and keep the manual available in the area where the
injector will be used. This manual contains important information about the safe operation of the injector.
Imaxeon urges the operators of the injector to read this manual carefully, become familiar with the injector
functions it describes, and follow its recommended procedures.
The injector is offered in Single and Dual syringe versions. General operations common to both are described,
and where the feature is specific to the Dual model, this is noted by [Dual Only].
2.3. Certifications
This injector is equipped to operate at 100 – 230 V~, 50/60 Hz, and is designed to comply with EN 60601-1 Ed
3.1 (safety) and EN 60601-1-2 Ed 4.0 (EMC/Emissions) standards.
Imaxeon Pty Ltd is EN ISO 13485:2016 certified.
2.4. Intended Use
The injector is intended to be used specifically for the purposes of venous injections of contrast agents and
common flushing solutions [Dual Only] into adult and pediatric patients during x-ray imaging procedures. DO
NOT attempt to use the injector for any other purpose.
2.5. Contraindications
This device is not to be used for drug infusion, chemotherapy, or any other use for which the device is not
indicated.
2.6. Trademarks
Bayer, the Bayer Cross, Imaxeon, MEDRAD FluiDots, MEDRAD Salient, MEDRAD, Salient and FluiDots are
trademarks owned by and/or registered to Bayer in the U.S. and/or other countries.
2.7. Disclaimers
This manual describes the use, operation and preventive maintenance needs of the MEDRAD
®
Salient Contrast
Injector, herein referred to as “the injector”. Qualified and trained personnel should only use the injector. Use by
unqualified and untrained personnel could result in patient or personal injury and property damage.