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Contact Us to Register Your Interest Already a member.Il rappresentante legale ESAOTE. ESAOTE legal representative. Le representant legal de ESAOTE. ESAOTE autorisierter Bevollmachtiger. El representante legal de ESAOTE. Page 5 USAGE LICENSE AGREEMENT FOR THE SOFTWARE INCLUDED IN THE APPARATUS Attention Please read with care the terms and conditions indicated below before using the software on the unit. Use of the software implies acceptance of the terms and conditions listed below. Such software products (“SOFTWARE”), as well as associated media, printed materials, and “online” or electronic documentation are protected by international intellectual property laws and treaties. The SOFTWARE is licensed, not sold. The SOFTWARE and, similarly, any copyrights and all industrial and intellectual ownership rights are and shall remain the exclusive propriety of Esaote S.p.A. or its Software Suppliers. The user will acquire no title or right on the SOFTWARE, except for the usage license granted herein. LICENSE RIGHTS AND LIMITATIONS With this license, Esaote S.p.A. grants the end user the right to use the SOFTWARE on the supplied DEVICE. On the basis of the above, and if the SOFTWARE is not protected against copying, only one copy of the SOFTWARE may be made for security purposes (back up copy). The user may not rent or lease the SOFTWARE, but he may transfer, on a permanent basis, the rights granted herein, on condition that he transfers all copies of the SOFTWARE and all written material, and that the transferee accepts all the conditions of this agreement. Any transfer must include the most up-todate version and all the previous ones. The user may not convert, decode, reverse-engineer, disassemble or change in any way the SOFTWARE. The user may not remove, obscure or alter the copyright notice, trademarks or other proprietary rights notices affixed to or contained within the SOFTWARE.
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The user may not publish data or information comparing the performances of said SOFTWARE with that of software written by others. Please use a duly filled copy of the form reported below or send us a communication reporting the same data indicated in this form. All data relating to the system can be found on its identification label. All data relating to the system can be found on its identification label. In this way we will be able to take all adequate measures with the best efficiency and timing. For US Customers: US Federal Law restricts this device to sale, distribution and use by or on the order of a physician. A-1 Product Specifications. A-1 Probe Specifications. A-5 Software Licenses and Kits. A-5 System Accessories. A-5 Appendix B - Installation. B-1 The CARIS PLUS Rear Panel. B-1 To Install the Mainframe Configuration. B-2 Requirements for Video Peripherals. B-3 Hard-copy Devices Installation. B-5 Digital Peripherals. B-6 Appendix C - Acoustic Output Data. C-1 Acoustic Output Tables. C-1 Acoustic Output Data according to IEC1157. C-24 Appendix D - Cleaning, Disinfecting and Maintenance. D-1 Equipment. D-1 Periodic Maintenance Schedule. D-1 Procedures. D-2 Appendix E - Cardiac Calculation Package. E-1 Measurements Accuracy and Formulas.E-1 Derived Data.E-2 Appendix F - Other Calculation Packages.F-1 Measurements Accuracy and Formulas.F-1 Derived Data.F-2 Gestational Age: References, Tables and Formulas.F-4 Appendix G - The VTR Menu and Off-Line Calculations.G-1 The VTR Menu. G-1 Off-Line Measurements. G-2 Appendix H - Older Probes Acoustic Data.H-1 According to FDA. H-1 Acoustic Output Data according to IEC1157. Intended Clinical Use Appendix A lists product and probes specifications.
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The following table lists the CARIS PLUS probes1 and their intended clinical use: CAR PV NH SP ABD OB PED PA Probes PA for Phased Array, LA for Linear and CA for Convex Array PA230E PA121E PA122E PA023E LA Probes LA522 LA523 CA Probes CARIS PLUS endocavity probes and applications are described later in this Operator’s Manual (Section 5). This system is not intended for transorbital or any other ophtalmic application. 1 Older generation probes which are compatible with the CARIS PLUS are described separately in Appendix H. 1 -1 Page 26 U S E R M A N U A L - CARIS PLUS Cardiac Application The probe applies ultrasound energy through the chest wall to obtain an image of the heart for purpose of assessing cardiac abnormalities. In Doppler modes, the probe applies energy through the chest wall to determine the velocity and direction of blood in the heart and in the vessels. Vascular Application The probe applies ultrasound energy through the neck or extremities of a patient to obtain an image of the carotid artery, or other peripheral vessels, that can be used to detect abnormalities or obstructions in the vessels. In Doppler modes, the probe applies ultrasound energy through the neck or extremities of a patient to assess the blood velocity, flow or lack of flow and patency of peripheral vessels. Abdominal Application The probe applies ultrasound energy through the patient abdomen to obtain an image of the abdominal organs to detect abnormalities (imaging) and assess the blood velocity, flow and patency of abdominal vessels through the Doppler modalities. Small Parts Application The probe applies ultrasound energy through the skin to obtain an image or a Doppler flow visualization of small organs such as thyroid (neck), testicles (scrotal sac) and breast (breast). In Doppler modes, the probe applies energy through the patient abdomen to detect placental or fetal flow abnormalities.
Use the lowest amount of acoustic output power for the shortest duration of time to obtain the necessary clinical diagnostic information. Neonatal Head The probe applies ultrasound energy through the neonatal head fontanelles to visualize brain structures (imaging) or flow (Doppler) to detect structural or functional abnormalities. A CAUTION describes the precautions which are necessary to protect the equipment. Be sure that you understand and observe each of the cautions and warnings. Electrical Safety As defined in EN60601-1 (IEC Standard 60601-1, Safety of Medical Electrical Equipment), this equipment is classified as Class I, with applied parts of type B (probes), and of Type CF (ECG). Do not remove the system or the monitor cover. Do not use the system in the presence of flammable anaesthetics. Pacemakers could interfere with these signals. You should be aware of this small potential hazard and immediately turn off the unit if interference with the pacemaker operation is noted or suspected. 1 -3 Page 28 U S E R Damages caused by dropping a probe, striking it against another object, pinching, kicking or twisting the cable are not covered under warranty. Follow the instructions in this Manual to install such a device. Wrong connections may compromize the electrical safety of the system. Wrong connections or the use of peripherals with improper safety characteristics may compromize the electrical safety of the system. Read carefully the appropriate sections of this Operator Manual before using any function labeled with this symbol. Environmental Safety Electro-magnetic Compatibility This system complies with the EN60601-1-2 (Electro-magnetic Compatibility). It is a Class A device. Note This is a class A product. In a domestic environment this product may cause radio interference; in this case the user may be required to take adequate measures. Sensitivity to interferences is more noticable in Doppler modalities.
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Ultrasound units are designed to receive radiofrequency (RF) energy and are, therefore, susceptible to other RF sources. In the presence of RF interference, the physician must evaluate the image degradation and its diagnostic impact. Electro-Surgical Units (ESUs) Electrosurgical units or other devices that introduce radiofrequency electromagnetic fields or currents into the patient, may interfere with the 1 -5 Page 30 U S E R M A N U A L - CARIS PLUS ultrasound image. An electrosurgical device in use during ultrasound imaging will grossly affect the 2D image and render Doppler modalities useless. Depending on the dimensions of a recyclable component, this symbol and the component’s material are applied to the component by ESAOTE. In this system, the packing materials are reusable and recyclable; the unit and display devices casings (plastic) and most of the cart components (plastic) are also recyclable. To remove the battery, contact ESAOTE personnel. The unit contains a Lithium Carbon MonoFluoride battery; the battery and the LCD screen must be treated as special garbage and, therefore, disposed of according to local regulations. Biocompatibility and Infection Control Items in Contact with Patient The probe and electrode material that is in contact with patients, complies with the European applicable requirements (EN30993). No negative reactions to these materials have been reported. Note ESAOTE probes and electrodes do NOT contain Latex. Probes and recommended consumables (gel and electrodes) are designed to be used on intact skin Refer to Appendix A for recommended Ultrasound Gels and single use electrodes or make sure you are using items which complies with applicable safety regulations.
Infection Control Regard any exam waste as potentially infectious and dispose of it accordingly Since probes and electrodes are intended to be used on intact skin, the use of this system has very limited probabilities to propagate infections; basic procedures as described later in this Manual are sufficient for infection control. 1 -6 Page 31 U S E R M A N U A L - CARIS PLUS Ultrasound Safety Introduction In compliance with the EN61157, Appendix C provides data about the acoustic power levels. Background information may be requested directly from ESAOTE. ESAOTE has adopted the more recent requirements and recommendations established by the USA Food and Drug Administration and by the American Institute of Medicine and Biology. The CARIS PLUS is, therefore, equipped with the Acoustic Output Display feature to provide the user with real-time, on-line information on the actual power of the system. The following sections describe the rationale of this methodology. ESAOTE recommends the use of the ALARA principle (see below), which is extensively covered in this Manual. Refer to the glossary at the end of this chapter for specific terms. In the USA, in more than three decades of use, there has been no report of injury to patients or operators from medical ultrasound equipment. Clinical Safety American Institute for Ultrasound in Medicine (AIUM) Statement on Clinical Safety: October 1982, Revised March 1983 and October 1983. Diagnostic ultrasound has been in use for over 25 years. Given its known benefits and recognized efficacy for medical diagnosis, including use during human pregnancy, the American Institute of Ultrasound in Medicine herein addresses the clinical safety of such use: No confirmed biological effects on patients or instrument operators caused by exposure at intensities typical of present diagnostic ultrasound instruments have been reported.
Although the possibility exists that such biological effects may be identified in the future, current data indicate that the benefits to patients deriving from the prudent use of diagnostic ultrasound outweigh the risks, if any, that may be present. The ALARA (As Low As Reasonably Achievable) principle is the guideline for prudent use: during an exam, the user should use for the shortest duration the least amount of acoustic output to obtain the necessary clinical information for diagnostic purposes. Ultrasound Bioeffects Although diagnostic ultrasound has an excellent history of safety, it has been known for a long time that ultrasound, at certain levels, can alter biological systems. 1 -7 Page 32 U S E R M A N U A L - CARIS PLUS The AIUM Bioeffects Committee describes two fundamental mechanisms by which ultrasound may induce biological effects: non-thermal or mechanical mechanisms2 and thermal effects. MECHANICAL BIOEFFECTS “Cavitation” phenomenon Non-thermal bioeffects, also referred to as mechanical bioeffects, seem to be caused by the tissue alternate expansion and contraction induced when ultrasound pressure waves pass through or near gas. The majority of these non-thermal interactions, also known as cavitation, deal with the generation, growth, vibration, and possible collapse of microbubbles within the tissue. The occurrence of cavitation depends on a number of factors, such as the ultrasonic pressure and frequency, the ultrasonic field (focused or unfocused, pulsed or continuous), the nature and state of the tissue and boundaries. Mechanical bioeffects are a threshold phenomenon, occurring only when a certain level of output is exceeded. However, the threshold level varies depending on the tissue. The potential for mechanical effects is thought to increase as peak rarefactional pressure increases, but to decrease as the ultrasound frequency increases.
Although there have been no adverse mechanical bioeffects in humans from diagnostic ultrasound exposure, it is not possible to specify thresholds at which cavitation will occur in mammals. THERMAL BIOEFFECT Rise in temperature of tissue exposed to acoustic energy. Thermal bioeffect is the rise in temperature of tissue when exposed to acoustic energy. The acoustic energy is absorbed by body tissue; absorption is the convertion of this energy into heat. If the rate of energy deposition in a particular region exceeds the ability to dissipate the heat, the local temperature will rise. The rise in temperature will depend on the amount of energy, the volume of exposure, and the thermal characteristics of the tissue. On-Screen Real-Time Acoustic Output Display Until recently, application-specific output limits3 established by the USA Food and Drug Administration (FDA) and the user's knowledge of equipment controls and patient body characteristics have been the means of minimizing exposure. Now, more information is available through a new feature, named the Acoustic Output Display. The Output Display provides users with information that can be specifically applied to ALARA. It eliminates some of the guess work and provides both an indication of what may actually be happening within the patient (i.e. the potential for bioeffects), and what occurs when system control settings are changed. Discover everything Scribd has to offer, including books and audiobooks from major publishers. Start Free Trial Cancel anytime.
Report this Document Download Now save Save Esaote Caris 7200 Service manual7200S01c For Later 0 ratings 0 found this document useful (0 votes) 403 views 4 pages Esaote Caris 7200 Service manual7200S01c Uploaded by Anonymous t1FCvPRSa Description: Esaote Caris 7200 Service manual Full description save Save Esaote Caris 7200 Service manual7200S01c For Later 0 0 found this document useful, Mark this document as useful 0 0 found this document not useful, Mark this document as not useful Embed Share Print Download Now Jump to Page You are on page 1 of 4 Search inside document Browse Books Site Directory Site Language: English Change Language English Change Language. The documentation is delivered in the format of a PDF portfolio, which provides thumbnails for each of the documents included in the application. Each thumbnail represents a different document. It is recommended that you use Adobe Reader to view this file as the portfolio functionality may not be handled well by all PDF viewers. Also, the instructions below are specific to Adobe and some functionality may be different or not available in other PDF viewers. PDF portfolios cannot be viewed in Microsoft Edge 25. You can preview a document by double-clicking a thumbnail. When in preview mode, a toolbar is displayed for navigating in the document. Button Description Extract file Save the document to a user-specified location. The file name will default to the name of the PDF when it was added to the portfolio. Show info view Display file information about the current selected thumbnail, such as the name and size of the file. Show previous page Display the previous page in the document. Show next page Display the next page in the document. Click the Left arrow button to preview the previous document and the Right arrow button to preview the next document. Exit (X) The X button in the top-right corner of the previewed document is used to exit preview mode.
This file can be launched from the Windows Start screen using the CARIS Application Documentation item if the application is not running. Procedure: Open a Document Original documents can be opened in a PDF viewer by selecting the Open File command or by double-clicking a file that is being previewed. A list of the documents containing the search term is displayed. Each document in the list can be expanded to show each instance of the search term in the document. 2. Click an item in the search results to preview the selected topic. The selected topic is displayed. You can browse the through list of results using the Left and Right arrow buttons beside the Search field. As you change topics, the name of the current document is displayed below the toolbar, which also provides a Close Preview button to return to the portfolio view. The toolbar in this mode provides additional tools to print or save the current document. 3. Click Close Preview to return to the portfolio view. Talk to an expert Today. (440) 459-1625 Using innovation and the latest research in ultrasound technology, Biosound has a reputation for providing high quality images. The ultrasound technicians at Providian Medical Field Service are prepared to service your Biosound AU3 ultrasound unit, Biosound Caris and Caris Plus equipment, Biosound Mega ES ultrasound machine, or your Biosound MyLab 30CV ultrasound system. Contact Providian today to speak to an ultrasound tech about your Biosound servicing needs. With technicians across 11 regions, you can expect your Biosound servicing, repair, and maintenance needs to be taken care of at your location. Schedule your Biosound preventive maintenance, or discuss your Biosound repair needs with our technicians today. Our service contracts for maintenance and repair of Biosound ultrasound equipment can be tailored to meet your servicing needs.
Service and maintenance contracts can include preventive maintenance visits, single year or multi-year contracts, probe testing, and a 24 hour or less on site response time service. Our experienced ultrasound engineers provide professional service at an affordable price. Contact Providian today for more information on Biosound ultrasound service contract options. Providian has a number of Biosound ultrasound service manuals to help with straightforward Biosound repair issues that can be repaired independently. Contact us today for your Biosound service manual needs. Suite A Chagrin Falls, OH 44022 Our videos have beed used by Doctors over 100,000 times. How I can change Display resolution on this ultrasound?,Service menu?,Service manual?,inside Dipswitch?.Please help me ! I have a device with lost configuration by RTC battery faukl. Without the configuration disk I can not establish the serial number or the licenses acquired Sign up now. Everything is ok so far. Previously I was convinced by Thomas that the language can be configured to the English version, but it wasn\'t. I already consult with local BBraun Engineer but they said impossible unless I replace the new mainboard. I was asking Thomas to return this product but he never replied. I bought Agfa 5302 and Carestream dryview 5850 from Thomas Konigbauer. Both devices are of good condition. I did receive it. Everything is ok I guess. But as an advise I mentioned many times I was looking for A NEW ITEM.Effectivement j\'ai achete le colposcope de la societe MED IT. J’ai recu le colposcope a Paris. Please note, that we are your international trading partner, we care for packing, transport and customs clearence Used: Article has already been used. An article with signs of wear but in good condition and fully functional. The item may be a demonstration model or an item returned to the seller after use Price of item does not include VAT, but is subject to differential taxation.
Shipping: EUR 400,00 Upon receipt of the item, the purchase must be cancelled within the grace period of 14 days. Shippingcosts are paid by the buyer Please note, that we are your international trading partner, we care for packing, transport and customs clearence Used: Article has already been used. An article with signs of wear but in good condition and fully functional. The item may be a demonstration model or an item returned to the seller after use Price of item does not include VAT, but is subject to differential taxation. Shipping: EUR 400,00 Upon receipt of the item, the purchase must be cancelled within the grace period of 14 days. Shippingcosts are paid by the buyer For doctors, dentists, veterinarians, pharmacists, hospitals, clinics and all persons interested in health. Free registration. Fast search function by subject area or category. Whether protective clothing, protective mask, Respirator mask FFP2, infrared thermometer or clinical thermometer - on doc-market you will find products of the brands Omron, 3M and many more. Calculate the costs for the publication of your ad with the quick calculator. If your place of work is not a government office, you will require a special secure account to access CARIS or any other online services. This account is a BCeID account. BCeID is an online service that makes it possible for you to use one Login ID and password to sign in securely to BCeID participating Government online services. BCeID accounts will automatically de-activate after three months of inactivity. This document describes the process for setting up a BCeID account and getting access to CARIS. Creating BCeID Account The BCeID request form is online. 1. Go to 2. Click Register for a BCeID under Registration (in the top right).S:\PS-Youth Forensic\Program Support\Client Information System\CARIS\User Manual\Business Process Manual\Web-publications\Contractor Accounts and Access.
doc 1 of 6 last saved on 2008-Feb-19 CARIS - Youth Forensic Psychiatric Services Contractor Accounts and Access.doc 4. Fill in the required information in all four steps and click Next to advance through the screens.When asked for Business Type, indicate Proprietor.When asked to provide a Password, consult the Password Guidelines to ensure protection to the information you will be accessing. The Password Reset Details are questions to verify your identity in case you forget your password. It is strongly recommended that you retain this information for future reference (needing to change your password etc.) c) Step 3 Business Details: Fill in the required information. Take note of or print the Point Of Service Location closest to verify your identity and residential address to activate your account.Enter their Last and First Name and the Region should be Provincial Services.If this section is not available, the Employment Status on the previous tab is not correct. 8. Click OK and an email is generated with the Security Access Request. 9. Include all CARIS locations required (a list for each region is on page 4) within the Add any Additional Comments here: area of the email. These will be sought out and then returned to this email account. 3. When the request has all the necessary approvals, it will be forwarded to the MCF Security ID Admin MCF:EX account to be completed. 4. You will receive confirmation of request received AND notification when it is completed. S:\PS-Youth Forensic\Program Support\Client Information System\CARIS\User Manual\Business Process Manual\Web-publications\Contractor Accounts and Access.doc 4 of 6 last saved on 2008-Feb-19 CARIS - Youth Forensic Psychiatric Services Contractor Accounts and Access.doc CARIS Locations by Region Include all required locations with each security request. All users need access to include access to IAU.
S:\PS-Youth Forensic\Program Support\Client Information System\CARIS\User Manual\Business Process Manual\Web-publications\Contractor Accounts and Access.doc 6 of 6 last saved on 2008-Feb-19 We are a non-profit group that run this service to share documents. We need your help to maintenance and improve this website. Biosound Megas Ultrasound System with phased array probes, model 7250 All Megas units with PA122 or PA023 probes. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.It is possible that some links will connect you to content onlyIn the case of any discrepancy in meaning, the English version is considered official. Thank. Please upgrade your browser to improve your experience. With results back in about 8 days, we’ll help you find better answers when you need it most. The technology platforms used and biomarkers tested may vary based on the tumor type submitted.Turnaround time for Caris profiling is 8-14 days. We understand that clinicians need treatment information fast. That’s why the top page of every report presents all potentially relevant, actionable clinical information in an easy-to-digest summary. Our Comprehensive Tumor Profiling approach to assess DNA, RNA and Proteins reveals a molecular blueprint to guide more precise and individualized treatment decisions. As such, Caris examines DNA, RNA and proteins to decode a patient’s tumor and provide a more comprehensive tumor assessment. One technology may not be sufficient or clinically appropriate to provide an integrated picture of a tumor’s biology. Learn more about our profiling technologies. View a sample report. Our laboratory holds the industry’s strictest quality and compliance accreditations, including ISO 15189, CAP, CLIA, NY State and CE Mark.
It was assumed that cultural and contextual factors would influence HCPs’ knowledge, attitudes, and practices in the clinical care of sexual assault survivors, and subsequently, their uptake of the training. Therefore, study settings were purposively selected to demonstrate the effectiveness of the CCSAS Multimedia Training Tool in a diversity of humanitarian settings, health facility levels, and geographical regions. Study settings included an IRC operated hospital in Dadaab Refugee Camp, Kenya, two government operated hospitals in Sheder and My’Ayni Refugee Camps in Ethiopia, two health facilities operated by a local non-governmental organization in an urban refugee setting in Amman, Jordan, and two referral hospitals and twenty-eight health posts operated by the government in post-conflict settings in Kabare and Kalehe health zones, South Kivu, Democratic Republic of Congo. All study sites, except Jordan, demonstrated previous documented cases of sexual violence in health facilities and all study sites had no previous training for health facility staff on clinical care for sexual assault, although some had received related training on gender based violence. Study design A mixed-methods study evaluated changes in HCP knowledge, confidence, attitudes, and practices pre and three months post CCSAS training. Data was collected through clinician questionnaires and in-depth interviews with HCPs and medical record audits. Tools were adapted to the local context and translated into the local language. The in-depth interview field guide was designed to qualitatively explore HCPs’ knowledge, confidence, attitudes, and practices caring for survivors of sexual assault. Interviews were conducted in English by the PI with interpretation in Amharic, Arabic, French, Somali, or Tigrinya as necessary by multilingual research staff trained in interpretation. Some interviews were conducted in French by a bilingual co-investigator without the use of interpreters.