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
88 MEDRAD
®
Salient Operation Manual
8.7. Connectors
Head Cable 26-way D sub-miniature
Hand/Foot Switch Circular, locking. 3 pin XLR
Line Power IEC 60320-C14
Equipotential Point MC POAG-S6 SERIES
Syringe Heater 4 pin Mini-DIN
8.8. IEC 60601-1 Classifications
The Injector is classified as follows:
♦ Class 1 equipment with Type BF applied parts.
♦ Internally Powered Equipment
♦ IPX0 (Injector and hand-switch) Clause 6.3 of IEC60601-1: 2005 (Injector head)
♦ IP68 (footswitch)
♦ Continuous Operation
♦ Not suitable for use in the presence of flammable anaesthetic mixtures with air or oxygen or nitrous
oxide
8.9. Ground Continuity
The resistance from the earth ground connector at the plug-end of the AC power cord to any grounded exposed
metal is less than 0.2Ω.
8.10. RoHS Statement
This injector meets the Directive 2002/95/EC of the European Parliament and of the Council of 27 January 2003
on the restriction of the use of certain hazardous substances in electrical and electronic equipment (RoHS). The
injector, with the exception of the battery, does not contain any of the following banned substances.
♦ Mercury
♦ Hexavalent Chromium
♦ Cadmium
♦ Polybrominated Biphenyls
♦ Polybrominated Diphenyl Ether
♦ Pentabromodiphenyl ether (PentaBDE)
♦ Octabromodiphenyl ether (OctaBDE)
♦ Decabromodiphenyl ether (DecaBDE)
Refer to Section 6.4 for details of the hazardous material contained in the battery.