Philips Ie33 User Manual
. U l t r a s o u n d S y s t e m User Manual 4535 616 23901 Rev A April 2012 © 2012 Koninklijke Philips Electronics N.V. All rights reserved. Published in USA. Philips Legal Department.
This document is intended to be used by customers and is licensed to them as part of their Philips equipment purchase. Use of this document by unauthorized persons is strictly prohibited. Customer Service.23 Recycling, Reuse, and Disposal.23 Safety.27 Basic Safety.27 Electrical Safety.28 Defibrillators.31 Fire Safety.32 Mechanical Safety.32 Equipment Protection.33 Product Compatibility.34 Symbols.35 Biological Safety.44 FDA Medical Alert on Latex.46 ALARA Education Program.47 Output Display.52 Control Effects.56 iE33 User Manual 4535 616 23901. Approved Accessories for Electromagnetic Compliance.73 Electromagnetic Immunity.75 Electromagnetic Interference.78 Recommended Separation Distance.80 Avoiding Electromagnetic Interference.82 Use Restrictions Due to Interference.83 System Overview.85 System Capabilities.85 Measurements.85 Transducer Types.86 Image Acquisition and Review.86 Patient Data Protection.86 System Options.87 Imaging Options.87 iE33 User Manual 4535 616 23901. Connecting an External Printer.107 Connecting the Foot Switch.109 External VCRs.110 Connecting an External VCR.111 Configuring Print Functions.111 Connecting an External Color Monitor.113 Connecting the System to a Network.113 Moving the System.114 Preparing and Moving.115 iE33 User Manual 4535 616 23901.
Touch Screen Controls.140 Touch Screen Knob Displays.144 Using the Retractable Keyboard.145 Status Icons.146 Voice Control.148 Voice Control Icons.150 Turning Headsets On and Off.151 Pairing Headsets.151 Configuring Headsets.153 Muting the Headset.154 Enabling Voice Control.154 Voice Profiles.154 iE33 User Manual 4535 616 23901. Setting the Auto Freeze Function.169 Transducer Receptacles and Cable Management.169 Connecting Transducers.170 Selecting a Transducer.173 ECG Feature.173 DVD, CD, and USB Devices.173 Media Compatibility.174 DVD Drive.174 Loading and Ejecting a Disc.175 Erasing a DVD.175 USB Devices.176 iE33 User Manual 4535 616 23901. Selecting in the Worklist.189 Searching in the Worklist.190 Selecting a Transducer.190 Imaging Modes.191 Using 2D Mode.191 Annotation.192 Adding Labels Using Annot.192 Adding Labels Using the Keyboard.193 Adding an Image Title.194 Displaying Body Markers.194 Recording.195 iE33 User Manual 4535 616 23901. Indications for Use and Supporting Transducers.208 xMatrix Array Transducers.210 X3-1 Description.210 X5-1 Description.211 X7-2 Description.211 Compact Transducer Adapter.211 Using the Compact Adapter.212 Transducer Maintenance.213 Acoustic Artifacts.214 Acoustic Artifacts in 3D Imaging.217 Transducer Covers.218 Ergonomic Grip.219 Installing the Ergonomic Grip.219 iE33 User Manual 4535 616 23901.
Leakage Current and TEE Transducers.246 Reducing Risks of Using TEE Transducers.246 TEE Deflection Control Basics.247 Connecting an S7-2omni, S7-3t, S8-3t, or X7-2t Transducer.248 Connecting a T6H or T6207 Transducer.249 S7-2omni TEE Transducer Description.250 iE33 User Manual 4535 616 23901. Checking the TEE Transducer.281 TEE Transducer Inspection.282 TEE Transducer Controls Inspection.282 Special Considerations for TEE Studies.282 Patient Selection for TEE Transducer Use.283 Preparing Patients for TEE Studies.284 TEE Study Guidelines.285 Tip Fold-Over.286 Recognizing Tip Fold-Over.286 iE33 User Manual 4535 616 23901.
Acoustic Coupling Medium.301 Choosing a Disinfectant.301 General Cleaning for All Transducers.302 Cleaning a Transducer.303 Disinfecting Transducers Using a Wipe or Spray Method.303 Cleaning and Disinfecting Cables and Connectors.306 Disinfection of Transducers by Immersion (High-Level Disinfection).309 iE33 User Manual 4535 616 23901. Specifying and Resetting the Air Filter Maintenance Status.337 Transducer Maintenance.338 Printer Maintenance.338 VCR and DVD Recorder Maintenance.339 Troubleshooting.340 Error Messages.341 Test Patterns.342 Transferring the Test Patterns.342 Using the Test Patterns.342 Testing the System.343 For Assistance.344 13 Specifications.345 iE33 User Manual 4535 616 23901.
Contents Safety and Regulatory Requirements.348 Index.351 iE33 User Manual 4535 616 23901. 1 Read This First This manual is intended to assist you with the safe and effective operation of your Philips product.
Before attempting to operate the product, read this manual and strictly observe all warnings and cautions. Pay special attention to the information in the 'Safety'. Read This First Use of the product for purposes other than those intended and expressly stated by Philips, as well as incorrect use or operation, may relieve Philips or its agents from all or some responsibility for resultant noncompliance, damage, or injury.
The Philips iE33 is one of the leading cardiovascular ultrasounds available. For pricing and iE33 transducer information, call Providian Medical today. Philips iE33. Quick Guide – QLAB 9 Cardiac Motion/Mechanics Quantification (CMQ) Overview / Introduction What is CMQ? The CMQ 9 provides a robust and objective. Community forums for Philips - iE33 Echocardiography relating to iE33 user manual on MedWrench.
User Manual: Provided with the product and included on the CD. The User Manual introduces you to features and concepts, helps you set up your iE33 User Manual 4535 616 23901. Shared Roles for System and Data Security: Included on the CD, it contains guidelines to help you understand how the security of your Philips product could be compromised and information on Philips' efforts to help you prevent security breaches. Where only one button in a group can be selected at a time, the selected button is indicated by a gold outline or background. For more information, see 'Touch Screen Controls' on page 140. IE33 User Manual 4535 616 23901.
Highlighting means to mark an image you want to reject during a protocol exam or an image you want to post-process. To highlight an image, click inside the image (but not on the number). IE33 User Manual 4535 616 23901. Customer Comments If you have questions about the user information, or you discover an error in the user information, in the USA, please call Philips at 800-722-9377; outside the USA, please call your local customer service representative.
IE33 User Manual. Telephone: 800-445-6741 (USA and Canada), +1 319-656-4447 (International) Fax: 877-329-2482 (USA and Canada), +1 319-656-4451 (International) E-mail: info@civco.com Internet: www.civco.com To order the items listed in the following table, see the referenced section and then contact your Philips representative. System Accessories Item Additional Information Cables 'Approved Cables for Electromagnetic. Customer Service Customer service representatives are available worldwide to answer questions and to provide maintenance and service.
Please contact your local Philips representative for assistance. You can also contact the following office for referral to a customer service representative, or visit the Philips Healthcare 'Contact Us'. Particularly, ensure that all the product-support documentation, including all instructions for use, are passed on to the new user. Make the new user aware of the support services that Philips Healthcare provides for installing, commissioning, and maintaining the system, and for comprehensive operator training. Recycling of useful materials by competent disposal companies. Safe and effective disposal of equipment For advice and information, contact your Philips service organization, or see the following website: www.philips.com/about/sustainability/recycling/productrecyclingservices/index.page Perchlorate Material In this system, perchlorate material is present in lithium coin cells or batteries.
Read This First iE33 User Manual 4535 616 23901. Do not use the system for any application until you are adequately and properly trained on its safe and effective operation. If you are unsure of your ability to operate the system safely and effectively, do not use it.
IE33 User Manual 4535 616 23901. Use the system only for its intended purposes. Do not use the system with any product that Philips does not recognize as compatible with the system. Operation of the product for unintended purposes, or with incompatible products, could lead to fatal or other serious injury. Do not use nonmedical peripherals, such as report printers, within 1.5 m (5 ft) of a patient, unless the nonmedical peripherals receive power from an isolated power outlet on the Philips ultrasound system, or from an isolation transformer that meets medical safety standards, as defined by standard IEC 60601-1-1. Connection of optional devices not supplied by Philips Ultrasound could result in electrical shock. When such optional devices are connected to your ultrasound system, ensure that the total system earth leakage current does not exceed 500 µA, or in the United States, 300 µA.
Use defibrillators that do not have grounded patient circuits. To determine whether a defibrillator patient circuit is grounded, see the defibrillator service guide, or consult a biomedical engineer. IE33 User Manual 4535 616 23901. The brakes are intended as a convenience. To increase cart security, use wheel chocks when the system is parked. If system operation is abnormal after you move or transport the system, contact Philips Ultrasound Customer Service immediately.
System iE33 User Manual 4535 616 23901. Improper cleaning or sterilization of a patient-applied part may cause permanent damage. For cleaning and disinfection instructions, see the 'Transducer Care' section. Do not submerge the transducer connector in solution. The cables and transducer bodies are liquid-tight, but the connectors are not.
IE33 User Manual 4535 616 23901. For information about such products and components, contact your Philips representative. Changes and additions to the system should be made only by Philips or by third parties expressly authorized by Philips to do so. Such changes and additions must comply with all applicable laws and regulations that have the force of law within the jurisdictions concerned, and best engineering practices. The International Electrotechnical Commission (IEC) has established a set of symbols for medical electronic equipment that classify a connection or warn of potential hazards. Of those symbols, the following may be used on your Philips product and its accessories and packaging.
Nonionizing electromagnetic radiation. Indicates that interference may occur in the vicinity of equipment marked with this symbol. The radio component contained in this device is compliant to Council Directive 1999/5/EC (Radio Equipment and Telecommunications Terminal Equipment Directive). IE33 User Manual 4535 616 23901. This degree of protection can apply to transducers and foot-operated devices. Indicates that the device is protected against the effects of immersion for up to 60 minutes. This degree of protection can apply to foot-operated devices.
IE33 User Manual 4535 616 23901. If the system is used stacked with or adjacent to other equipment, verify normal operation before use. Indicates the temperature range (noncondensing) for transport and storage.
(Does not apply to media.) iE33 User Manual 4535 616 23901. Indicates that the device is fragile; handle with care.
Do not use if damaged. Warns of system over-balance due to external force. (Do not push on the monitor or the transducer holders to move the system.) iE33 User Manual 4535 616 23901. Serial number.
Universal part number. The following symbols may also be used on the system and its accessories and packaging: Connection for a pencil probe Connection for a pencil probe Connection for a transducer iE33 User Manual 4535 616 23901. CD, or DVD Output port for audio left/right, VHS/S-VHS, video patient monitor, black-and-white printer, or interlaced RGB output port Input port VGA or parallel output port DVI video output receptacle USB input/output port iE33 User Manual 4535 616 23901. Isolated auxiliary power provided for connection of Philips-approved remote accessories. Foot switch Indicates the atmospheric pressure range for transport and storage. SVGA connectionTwo video receptacles provide DVI-D digital video for flat-panel monitors. S-Video connection iE33 User Manual 4535 616 23901.
Identifies the port for the PercuNav field generator. Chinese Environmentally Friendly Use Period symbol. UL (Underwriters Laboratories) classification symbol. CSA (CSA International) classification symbol. Indicates a possible pinch hazard when positioning the monitor. IE33 User Manual 4535 616 23901.
Perform ultrasound procedures prudently. Use the ALARA (as low as reasonably achievable) principle. Use only acoustic standoffs that have been approved by Philips Ultrasound. For information on ordering approved accessories, see 'Supplies and Accessories' on page. If the system becomes contaminated internally with bodily fluids carrying pathogens, you must immediately notify your Philips service representative. Components inside the system cannot be disinfected.
In that case, the system must be disposed of as biohazardous material in accordance with local or federal laws. Patients with positive histories should have their charts flagged. If latex sensitivity is suspected, consider using devices made with alternative materials, such as plastic. For example, a health professional could wear a iE33 User Manual 4535 616 23901. The ultrasound system and transducers described in this document do not contain natural rubber latex that contacts humans. Natural rubber latex is not used on any Philips ultrasound transducer. It also is not used on Philips ECG cables for the products described in this document.
The decision as to the amount of acoustic output is, in the final analysis, up to the system operator. This decision must be based on the following factors: type of patient, type of exam, patient history, ease or difficulty of obtaining iE33 User Manual 4535 616 23901. Direct Controls Application selection and the output-power control directly affect acoustic intensity.
There are different ranges of allowable intensity or output based on your selection. Selecting the correct range of acoustic intensity for the application iE33 User Manual 4535 616 23901. Pulse length is the time during which the ultrasonic burst is turned on. The longer the pulse, the greater the time-average intensity value. The greater the iE33 User Manual 4535 616 23901. Having acquired the 2D display of the liver, Color can be used to localize blood flow. As with the 2D image display, gain and image processing controls must be optimized before increasing output.
IE33 User Manual 4535 616 23901. The TIB, TIS, or TIC is continuously displayed over the range of 0.0 to maximum output, based on the transducer and application, in increments of 0.1. For the location of the output display, see 'Imaging Display' on page 166.
IE33 User Manual 4535 616 23901. MI value, the greater the likelihood of mechanical bioeffects occurring.
There is no specific MI value that means that a mechanical effect is actually occurring. The MI should be used as a guide for implementing the ALARA principle. IE33 User Manual 4535 616 23901. The values should not be interpreted as actual physical values in interrogated tissue or organs. The initial data that is used to support the output display is derived from laboratory measurements based on the American Institute of iE33 User Manual 4535 616 23901. 0.3 dB/cm-MHz rate, occur in water tank measurements or in most tissue paths in the body.
In the body, different tissues and organs have dissimilar attenuation characteristics. In water, there is almost iE33 User Manual 4535 616 23901. TI below the system maximums. A decrease in pulser voltage will decrease MI. Zoom: Increasing the zoom magnification by pressing Zoom may increase frame rate. This action will increase the TI.
The number of focal zones may iE33 User Manual 4535 616 23901. The TI will increase.
MI will change little, if at all. If PW Doppler is also enabled, then PW Doppler will remain the dominant mode and the TI change will be small. IE33 User Manual 4535 616 23901.
The MI displayed is that of the zone with the largest MI value. Application: Acoustic output defaults are set when you select an application.
Factory defaults vary with transducer, application, and mode. Defaults have been chosen below the FDA limits for intended use. IE33 User Manual 4535 616 23901. Another report, “Bioeffects and Safety of Diagnostic Ultrasound,” dated January 28, 1993, provides more-current information. The acoustic output for this system has been measured and calculated in accordance with the “Acoustic Output Measurement Standard for Diagnostic iE33 User Manual 4535 616 23901.
In Situ In Situ intensity value Water Water value intensity 2.7183 Attenuation factor Tissue a(dB/cm-MHz) Amniotic 0.006 Fluid Brain 0.53 Heart 0.66 Kidney 0.79 Liver 0.43 Muscle 0.55 Skin line to measurement depth (cm) iE33 User Manual 4535 616 23901. No single tissue model is adequate for predicting exposures in all situations from measurements made in water, and continued improvement and verification of these models is necessary for making exposure assessments for specific applications. IE33 User Manual 4535 616 23901.
“fixed-path” tissue model and are for devices having Ispta (derated) values greater than 500 mW/cm. The temperature elevations for fetal bone and tissue were computed based on calculation procedures iE33 User Manual 4535 616 23901. Wo is the ultrasonic power in milliwatts 6.2% (mW).
Is the center frequency in megahertz.
GMI is committed to empowering the Biomed community with outstanding training programs. We believe that the more knowledge that we can pass on to the community, the better off patients will be served. By providing cost effective, hands on and practical training, engineers are immediately able to impact the bottom line of day to day operations. Benefits of GMI Training.
Small Classes to increase Teacher to Student instruction time. Comprehensive Hands-On course instruction. 24/7 Technical Suport. Access to video training library. Cost Effective. Time saving course gets engineers back to work quickly. Best Instructors in the industry.
Ultrasound 101 Self-Pace video class. Preventive Maintenance instruction Can’t find what you are looking for? Call 800.958.9986 to speak to a qualified GMI representative. Enrollment To book a seat in a training course, please the enrollment form and send it with the purchase order to: Mailing Address: Global Medical Imaging (GMI) ATTN: Training Department 222 Rampart Street, Charlotte, NC 28203 Fax: (704) 940-7756 Email: training@gmi3.com. Other Payment Prepay options are accepted. Please refer to the enrollment form for details.
Start & Finish Times All classes begin promptly at 9:00 am and finish at 5:00 pm. Class Supplies Each student needs to come prepared with a notebook and writing utensil; PC is optional (All other study information will be provided by the ultrasound instructor). Cancellation Cancellations MUST be given fourteen days in advance. Location All courses take place at our Charlotte, NC facility at 222 Rampart Street. The nearest airport is Charlotte Douglas International (CLT). Can’t find what you are looking for?
Call 800.958.9986 to speak to a qualified GMI representative. Ultrasound 101 This course covers the basic physics and principles of ultrasound. The class provides the theory and understanding behind ultrasound operation. Basic system architecture, transducer types and their applications will also be discussed. Class gives background and fundamentals for ultrasound operation and lab provides hands on scanning techniques, scanning modes and knobology.
Course Outline. Basic Theory. Physics. System Architecture. Transducer Types and Applications The course is provided online & via the video library on the GMI website.Course is prerequisite for platform specific, unless attendee has 1 year of ultrasound experience.
Philips iU22/iE33 Service Training The iU22 and iE33 are the flagship ultrasound platforms manufactured by Philips. The iU22 is primarily a general imaging system while the iE33 is the premier cardiac system. Both systems offer excellent image quality and ergonomics. This platform is built on similar architecture of its predecessor the HDI 5000. The iU22/iE33 service training course is designed for the ultrasound service professional.
This course will focus on the system as it pertains to theory, architecture, block diagram and functional repair. Course Outline. Basic Theory. System Familiarization. Manual Overview. System Architecture-Common Failures.
System Software Revision. Cart Revision History. Software Reload and Upgrade Procedures. System Comparison. Troubleshooting-Replacement. PM Procedure. DICOM Connectivity The course is completely hands on with labs focusing on scanning techniques, common failures, and board/module replacement.Course prerequisite is 1 year of ultrasound experience or Ultrasound 101 course.
GE Logiq/Vivid E9 Service Training The Logiq E9 is the newest flagship Radiology ultrasound system manufactured by GE. The system produces outstanding images, has improved ergonomics and allows for integration of multiple modalities.
The Logiq E9 service training course is designed for the ultrasound service professional. This course will focus on the system as it pertains to theory, architecture, block diagram and functional repair. Course Outline. Basic Theory. System Familiarization. Manual Overview. System Architecture-Common Failures.
Troubleshooting-Replacement. PM Procedure.
DICOM Connectivity The course is completely hands on with technicians focusing on scanning techniques, common failures, and board/module replacement.Course prerequisite is 1 year of ultrasound experience or Ultrasound 101 course. S2000 Service Training The S2000 is a premium ultrasound imaging console. The system is built on next generation acoustic technologies that enable you to experience never-before-seen detail during examinations. The system software uses advanced algorithms and an expert database of real clinical cases to recognize anatomical patterns and landmarks as well as perform automatic measurements.
The S2000 is the replacement system for the Siemens Sequoia. The S2000 service training course is designed for the ultrasound service professional. This course will focus on the system as it pertains to theory, architecture, block diagram and functional repair. Course Outline. Basic Theory. System Familiarization. Manual Overview.
System Architecture-Common Failures. Troubleshooting-Replacement. PM Procedure. DICOM Connectivity The course is completely hands on with technicians focusing on scanning techniques, common failures, and board/module replacement.Course prerequisite is 1 year of ultrasound experience or Ultrasound 101 course. Philips EPIQ/Affiniti Service Training The Epiq 5/7 and Affiniti 50/70 are the newest offerings for the ultrasound modality manufactured by Philips.
The Epiq 5 & Affiniti 50 are primarily general imaging systems while the Epiq 7 and Affiniti 70 are the premier cardiac systems. Both series of systems offer excellent image quality and ergonomics. The platforms are built on similar architecture of their predecessor the iU22 & iE33. The Epiq/Affiniti service training course is designed for the ultrasound service professional. This course will focus on the system as it pertains to theory, architecture, block diagram and functional repair. Course Outline. Basic Theory.
System Familiarization. Workbook Overview. System Architecture-Common Failures. System Software Revision. Software Reload and Upgrade Procedures.
System Comparison. Troubleshooting-Replacement. PM Procedure. DICOM Connectivity The course is completely hands on with labs focusing on scanning techniques, common failures, and board/module replacement.Course prerequisite is 1 year of ultrasound experience or Ultrasound 101 course. GE Voluson E8 Service Training The Voluson E8 is one of the newest in the Voluson family of OB/GYN & Women’s Health ultrasound systems produced by GE. The system provides anatomical images never seen before, has improved ergonomics and improved automation. The Voluson E8 service training course is designed for the ultrasound service professional.
This course will focus on the system as it pertains to theory, architecture, block diagram and functional repair. Course Outline. Basic Theory. System Familiarization. Manual Overview. System Architecture-Common Failures. Troubleshooting-Replacement.
Philips Ie33 Echo Machine User Manual
PM Procedure. DICOM Connectivity The course is completely hands on with technicians focusing on scanning techniques, common failures, and board/module replacement.Course prerequisite is 1 year of ultrasound experience or Ultrasound 101 course. For Immediate Service, please call 800.958.9986 option 1 for 24×7 support Hours of Operation 8:30-5:30 M-F; 7:30 pm for parts EST Alternative Registration Form (PDF) You can the registration form and send it with the purchase order to: GMI ATTN: Training Department 222 Rampart Street Charlotte, NC 28203 Fax: (704) 940-7756 Note: Prepay options are accepted. Please refer to the enrollment form for details. Can’t find what you are looking for?
Call 800.958.9986 to speak to a qualified GMI representative.