haemonetics teg manual

haemonetics teg manual

By clicking the “ACCEPT” button to your right or by clicking on any site content, you agree to the placement of cookies on your computer. For more information, see our Privacy Policy. For more information, see our Privacy Policy. Featuring an innovative, all-in-one cartridge, the TEG 6s delivers the same quality test results without the complicated test preparation process. TEG 6s allows clinicians to drive personalized, clinically and economically sound treatment and monitoring decisions with confidence. New to the TEG system technology is the measurement of clot viscoelasticity using a resonance method. To measure the clot strength with the resonance method, the sample is exposed to a fixed vibration frequency. The frequency leading to resonance is identified and then converted to the TEG system readout. Stronger clots have higher resonant frequencies and higher TEG readouts. Preparing the blood sample for the TEG 6s system analysis is very simple. There is no need for controlled pipetting or prior manipulation of reagents. The only requirement is to transfer a small, unmetered amount of blood to the loaded cartridge from a sample tube with citrate or heparin. To check availability in your region, please contact us for more information. For more information, see our Privacy Policy. With two independent sample channels of a variety of tests, graphical and numerical data output, remote data viewing, and more, the TEG system has become the new standard of care in hemostasis management. Contact us for more information To be configured as follows. What’s your cost to treat an infection caused by an avoidable allogeneic transfusion. How often is your patient at risk for thrombosis. Traditional coagulation testing is proven, but limited Routine coagulation tests are used as a starting place when investigating the cause of bleeding. They indicate the time of fibrin formation through the intrinsic and extrinsic pathways of the coagulation cascade. While.http://tibbelit.se/userfiles/gateway-3040gz-manual.xml

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Facilitating or inhibiting platelet function before surgery — without understanding the patient’s baseline function — could put your patient at risk for a thrombotic or. By simply having a more thorough understanding of patients' hemostasis, unnecessary allogeneic transfusions could be avoided. Given that a TEG analysis can aid the prediction of a surgical bleed greater than 95% of the. PlateletMapping is a trademark of Cora Healthcare. Aspirin is a registered trademark of Bayer Aktiengesellschaft. 03.2010 THE Blood Management Company Prices are indicative only and may vary by country, with changes to the cost of raw materials and exchange rates. Haemonetics is ready to assist Laboratory Managers in developing an IQCP for the TEG based on the ISO Hazard Analysis, incorporating up to a once weekly external QC regimen. Pa de folgende sider vil. Presented by Suzanne M Hoffman MT (ASCP). Sorting options p Sort by haemonetics teg 5000 manual patient name p Sort by patient ID When you have selected one of these options, you can then specify whether the sorting should be ascending or descending, and click on Done. Mix specimen thoroughly by gentle inversion. The aim of this study was to assess agreement and interchangeability between the TEG6S and TEG analysers. Haemonetics won FDA clearance for its TEG 6s Hemostasis Analyzer System to be used in adult trauma settings to evaluate the viscoelasticity of patients’ blood. TEG Haemonetics U. This course is conducted on-line via the internet with a multi-media approach to remote learning, including interactive review and examination, along with embedded videos demonstrating PM procedure steps per the ACP. The TEG System facilitates your understanding of hemorrhagic or thrombotic risk by revealing: Rate of clot formation, Strength and stability of clot, Effect of platelet, coagulation factor, and cellular, interactions, Maximum platelet function. The Site Administrator can change the setting.http://cw-cut.com/uploads/file/gateway-400vtx-repair-manual.xml

This system is a compact diagnostic instrument that provides clinicians with rapid, comprehensive and accurate identification of a patient’s hemostasis. Please contact your local Haemonetics representative to establish haemonetics teg 5000 manual a free account for your hospital.S. nance and cleaning described in this manual is required, the local Haemonetics representative should be contacted to provide specific instruction. Product Details. ?. Haemonetics is committed to the protection of personal data in accordance with applicable laws and regulations.S. S. Page 7 Chapter 1: Only one captured image can be held on the clipboard at a time. Citrated kaolin thromboelastography (CK-TEG) assays were recalcified and run according to the manufacturer’s instructions on a TEG Thrombelastograph Hemostasis Analyzer (Haemonetics). Page 7 Chapter 1: Only one captured image can be held on the clipboard at a time. Mississippi Valley Regional Blood Center, USA, View all customer testimonials. Signy Centre Rue des Flecheres P. ?. Press the index key A to exit. By continuing. The letters listed guidelines regarding proper use of the TEG System Power Supply to eliminate any potential risks such as electrical shorting or power supply damage. New to the TEG system technology is the measurement haemonetics teg 5000 manual of clot viscoelasticity using a resonance method. Donelan D. nance and cleaning described in this manual is required, the local Haemonetics representative should be contacted to provide specific instruction. From our devices, to our integrated software solutions, to our value-added consulting services, we are committed to advancing the safety, quality, and availability of the world’s blood supply while helping to enhance the donor experience, improve patient care, and increase operational efficiencies. New to the TEG system technology is the measurement of clot viscoelasticity using a resonance method. They also use different chemicals.

The haemonetics teg 5000 manual information, which was printed in the letter, will also be available in an updated TEG User Manual soon to be released. 8 million Surgical million Whole Blood 40 million Automated Collections Manual Collections Welcome to Haemonetics. When a sample ends either manually or by program settingsit is removed from the TEG screen. Haemonetics TEG Technical Manual (). TEG Manager is an application that provides remote viewing of current and historical patient tracing and test results created by the TEG 6s analyzers, and administration of all connected TEG 6s devices. It would be most helpful to have your most recent electric bill handy for this. Haemonetics Software Download Center. Samples were run within one half to 1 hour of collection. The intent of each seminar is to familiarize biomedical engineers with maintenance and service procedures of our TEG systems, and is modeled after the same training received by Haemonetics Field Service Engineers. Rapid TEG reagent simultaneously activates the intrinsic and extrinsic coagulation pathways by adding tissue factor to the test system. The TEG 6s and TEG Manager are approved for the same set of indications in Europe, Australia and Japan. TEG Thrombelastograph Hemostasis Analyzer System. TED automatically resets the billing cycle based on the Meter Read Date. Lab Dept: Coagulation Test Name: TEG WITH HEPARINASE General Information Lab Order Codes: TEGH Fibrinolysins or coagulopathy screen, interpretation and report Test Includes: TEG parameters, R, K, Angle, MA, G, and LY30 evaluated with heparinase. Special Coagulation Laboratory University of Wisconsin Hospital and Clinics. Press the index key A to exit. Returned Goods Authorization system Haemonetics seeks to provide the apheresis customer with haemonetics teg 5000 manual equipment and mate-rial which respects the highest established standards of quality in design and.

Haemonetics won FDA clearance haemonetics teg 5000 manual for its TEG 6s Hemostasis Analyzer System to be used in adult trauma settings to evaluate the viscoelasticity of patients’ blood. Download Center. TEG and Haemonetics—pioneers of the. The information, which was printed in the letter, will also be available in an updated TEG User Manual soon to be released. To measure the clot strength with the resonance method, the sample is exposed to a fixed. The TEG Manager haemonetics teg 5000 manual is an optional accessory to Haemonetics TEG 6s Hemostasis System. Page Next, specify whether the data should be placed in an existing table or in a new table Figure 8. The TEG 6s system is easy to use for near-patient testing, and physicians can view both active and historical test. Logistics Haemonetics TEG Technical Manual (). Sample Preparation p Gloves Procedure 1. Collection: A clean venipuncture or line draw is essential. Product Downloads; Public IFU; Languages. Please contact your local Haemonetics representative to establish a free account for your hospital. However, if you approach the maximum size limit of 2GB, the database will stop working; the software will haemonetics teg 5000 manual give a warning before the 2GB maximum is reached. Signy Centre Rue des Flecheres P. Blood and Plasma Center Devices. Processed Volume: Same as Draw Volume Collection: A clean venipuncture or line draw is essential. This Home Design and Decorating Ideas site for your references. These settings affect the haemonetics teg 5000 manual rate calculations of your TED system. However, they provide similar haemonetics teg 5000 manual information on. Returned Goods Authorization system Haemonetics seeks to provide the apheresis customer with equipment and mate-rial which respects the highest established standards of quality in design and. By providing a more complete picture of your patients' hemostasis, the TEG system can.

Data from multiple devices can be centralized, with remote access to any connected TEG analyzer, no matter where it is located. Haemonetics - TEG AnalyzerUnique in its ability to detect the state, cause, and extent of imbalance in patient hemostasis and to provide guidance for effective.LaRose S, Croft R, Lawler D, and Wall-Donelan. SE Exakt Den nye generation af Digitale Fartskrivere Introduktion Med denne brochure vil vi gerne informere dig om vores nye generation af digital fartskriver SE Exakt.A. mL whole blood was collected Author: Patryck Lloyd-Donald, Leonid Churilov, Faizan Zia, Rinaldo Bellomo, Graeme K Hart, Peter R McCall, J. Both use different mechanisms to assess similar components of the coagulation process.A. A. It would be most helpful to have your most recent electric bill handy for this. The system relies on an all-in-one. However, if you approach the maximum size limit of 2GB, the database will stop working; the software will give a warning before the 2GB maximum is reached. The TEG Hemostasis Analyzer System provides a more complete picture of patients' hemostasis, thus helping you deliver more targeted treatment.S. The system relies on an all-in-one. We are continually advancing our thought leadership and research, enhancing our training resources, and building our library of educational materials to help ensure that you have a comprehensive array of resources to increase your knowledge about blood management. Haemonetics S. This decreases haemonetics teg 5000 manual the time it takes to form a clot, allowing for faster turnaround times. Transfer the blood gently from the syringe to a small non-wettable surface, e. This date may fluctuate from bill-to-bill by a couple of days (depending on weekends, etc). The program focuses on technical issues and provides an in-depth review of programming and protocols haemonetics teg 5000 manual to enable operators to troubleshoot haemonetics teg 5000 manual any potentially difficult problems.

Contact Us to Register Your Interest Already a member. Any information or descriptions contained in this manual may not be reproduced and released to any of the general public, or used in conjunction with any professional instructions without written consent of Haemonetics Corporation, USA. Disclaimer This manual is intended as a guide to provide the user with necessary instructions on the proper use and maintenance of certain Haemonetics Corporation products. This manual should be used in conjunction with instruction and training supplied by qualified Haemonetics personnel. Any failure to follow the instructions as described could result in impaired product function, injury to the user or others, or void applicable product warranties. Haemonetics accepts no responsibility for liability resulting from improper use or maintenance of its products. Utilization of Haemonetics products may require the user to handle and dispose of blood-contaminated material. Users must fully understand and implement all regulations governing the safe handling of blood products and waste, including the policies and procedures of their facility. Handling and use of any blood products collected or stored using Haemonetics equipment are subject to the decisions of the attending physician or other qualified medical personnel. Haemonetics makes no warranty with respect to such blood products. Patient diagnosis is the sole responsibility of the attending physician or other qualified medical personnel. The screenshots appearing in this manual are provided for illustrative purposes only, and may differ from the actual software screens. Any similarity to the name of an organization or person is unintentional. The TEG 6s analyzer is licensed for sale or use only in in-patient hospitals and any laboratories that are primary providers of such hospitals.

Document updates The document is furnished for information use only, is subject to change without notice and should not be construed as a commitment by Haemonetics Corporation. Haemonetics Corporation assumes no responsibility or liability for any errors or inaccuracies that may appear in the informational content contained in this material. For the purpose of clarity, Haemonetics Corporation considers only the most recent version of this document to be valid. Trademarks and patents Haemonetics, TEG, RapidTEG, and Thrombelastograph are trademarks or registered trademarks of Haemonetics Corporation in the US, other countries, or both. PlateletMapping is a registered trademark of Cora Healthcare, Inc. Vacutainer is a registered trademark of Becton, Dickinson and Company. US patent numbers 7,261,861, 7,879,615, 8,236,568, 6,787,363, 7,179,652, and 9,068,966. Note: Availability of devices may vary from one country or region to another as a result of specific local regulatory approval or clearance requirements. Applicable laws may restrict the sale, distribution, or use of this device to, by, or on the order of a licensed healthcare practitioner. Haemonetics worldwide Please direct any written inquiries to the appropriate address. This manual includes. A detailed description of the analyzer. ? Instructions for operating the analyzer and troubleshooting any difficulties. ? Information on how to properly handle and maintain the analyzer. ? Specifications and performance capabilities. Use this manual in combination with training supplied by qualified Haemonetics personnel. What is the TEG 6s system. The TEG Thrombelastograph hemostasis analyzer TEG 6s Series system consists of the following components. TEG 6s analyzer ? Disposable cartridges with preloaded dried reagents. Service-Maintenance-Settings (SMS) software interface The TEG analyzer monitors the harmonic motion of a pendant drop of blood in response to external vibration.

As the sample transitions from a liquid state to a gel-like state during clotting, the modulus of elasticity and resonant frequency increase. The analyzer measures these variations in resonant frequency during clotting and lysis and displays the results on a touchscreen display. Disposable cartridges are used for processing whole blood samples. Blood is delivered by transfer pipette to a small port in the cartridge. Once a sample has been added to the cartridge and testing has begun, the sample is inaccessible to the user. The cartridges contain all necessary reagents for performing an assay. The TEG analyzer has two modes of operation: (1) Stand-alone, and (2) computer-controlled through the network interface. Service-MaintenanceSettings (SMS) software provides the interface for an administrator or qualified service technician to change configuration settings, update, backup, and restore firmware and data files, and manage analyzer calibration parameters. For more information about the SMS software, consult the TEG 6s Site Administrator Guide. The TEG 6s analyzer is indicated for use with adult patients where an evaluation of blood coagulation properties is desired. Results from the TEG 6s analyzer should not be the sole basis for a patient diagnosis, but should be evaluated together with the patient’s medical history, the clinical picture and, if necessary, other coagulation tests. Precautions The operator should be aware of the following precautions. Read and understand the entire contents of this manual before operating the TEG analyzer - especially precautionary information and specifications. ? The TEG analyzer is to be operated by qualified personnel only. ? If this equipment is used in a manner inconsistent with this manual, protections provided by the device may be impaired. ? Use only Haemonetics parts and accessories with the TEG analyzer. Third-party accessories may cause improper performance. ? DO NOT use malfunctioning equipment.

Have the unit repaired by an authorized Haemonetics service representative. ? DO NOT place anything other than human blood, plasma or Quality Control (QC) material into a cartridge. ? Upon removal from the TEG analyzer, used cartridges must be immediately disposed of according to local standard operating procedures for the removal of biohazardous material and should not be mixed with non-biohazardous waste. Repair service Haemonetics maintains a worldwide network of company-trained service representatives responsible for responding to technical needs concerning equipment. If service beyond the routine maintenance and cleaning described in this manual is required, the local Haemonetics representative should be contacted to provide specific instruction. Preventive maintenance General maintenance procedures should be performed as required. For instructions, refer to “Cleaning and Disinfecting the Analyzer” on page 7-89. Preventive maintenance procedures should be conducted annually to ensure optimal mechanical functioning of the analyzer and are performed by a trained Haemonetics representative. Product return guidelines If, for any reason, merchandise must be returned to the company, the customer should contact the local Haemonetics representative to arrange for repairs or returns using procedures to ensure proper handling and subsequent analysis. No returns will be accepted without advanced authorization. Units returned to Haemonetics for repair are subject to biohazard charges if any component is contaminated with blood or blood products. Warning: Haemonetics products must be properly cleaned and packaged prior to their return. It remains an important responsibility of the customer to reduce potential health hazards by being aware of the risks involved in the shipping, handling and testing of this material. Note: provides useful information regarding a procedure or operating technique when using Haemonetics material.

Tip: provides additional information or an alternate method to perform a task when using Haemonetics material. Caution: advises the operator against initiating an action or creating a situation which could result in damage to equipment or impair the quality of the test results; personal injury is unlikely. Warning: advises the operator against initiating an action or creating a situation which could result in serious personal injury to the patient or operator. Symbols found on the analyzer and packaging The following symbols may appear on the analyzer, consumables, or packaging: Electrical and electronic equipment waste (applies to EU only) Dispose of the device using a separate collection method (according to EU and local regulation for waste electrical and electronic equipment). Color-coded top conforms to ISO 6710:1995. CE mark General warning, caution, risk of danger Biological risks Consult instructions for use (Applies to USA only) USA Federal Law restricts the sale, distribution or use of this device to, by or on the order of a physician. Exterior back components. Disposable assay cartridges Note: Any references made to “front” or “back” are from the perspective of an operator facing the TEG analyzer. The TEG 6s system consists of an analyzer and disposable assay cartridges. The analyzer contains a user-friendly interface in the form of a color touchenabled display. Through this interface, the operator can control all operations of the analyzer except turning it on and off, which is accomplished by accessing a switch at the rear of the analyzer. The system is designed to accept a disposable plastic cartridge, into which a blood sample can be placed. Once a test is started, the analyzer processes the sample and reports the results on the touchscreen display. All prompts, directions, selections, and results are displayed on this screen. Cartridge slot The cartridge slot at the front of the analyzer accepts TEG analyzer assay cartridges.

During a test, the cartridge is locked in place. When the test is complete, a lighted strip flashes around the perimeter of the cartridge slot. Cooling fan The fan on the back of the analyzer ensures that the internal temperature of the analyzer remains close to the ambient temperature. This allows the widest possible range of sample temperatures to be selected without requiring active cooling in the analyzer. USB ports Three Standard Type A USB ports are located to the left of the cooling fan and can be used to attach a peripheral device, such as a printer or barcode scanner, to the analyzer. LED lights on either side of the port have the following functions: Left LED - Link Speed Right LED - Link Activity. Amber: operating in 1000 BT mode. Blinking green: activity. Green: operating in 100 BT mode. Off: no link established. Off: operating in 10 BT mode Fuse holder The fuse holder is a cylindrical housing that protects and holds the fuse. Fuse The 250 Volt 5 Amp fuse is located inside the fuse holder on the back of the analyzer. Power jack The power jack is located at the back of the analyzer and is the screw-on connection point for the power cord that is supplied by Haemonetics. Do not replace the cord with a substitute. If necessary, contact the local Haemonetics representative for a replacement. Use an Uninterruptible Power Supply (UPS) unit between the analyzer and the power source. Grounding reliability can be achieved only when the analyzer is connected to a properly grounded outlet. Cartridges should be kept in their sealed pouches and in the specified storage conditions (2-8 deg C) until just before use. Cartridges can be used directly from the refrigerator; they do not need to reach room temperature before use. 1. Barcode 2. Sample port 1 2 Figure 3, TEG analyzer disposable assay cartridge Sample port A sample port at one end of the cartridge accepts an unmetered amount of blood, delivered by transfer pipette.

Under instrument control, the cartridge pulls the blood sample into up to four staging areas, mixes the sample with reagents that have been dried in place, and then transfers a small amount into the test cells. Excess blood is moved to a sealed waste area within the disposable. Barcode The barcode on the cartridge allows the analyzer to identify the cartridge type, test type, expiration date, and lot number. Cartridge Library In addition to the barcode on the cartridge, the analyzer system also uses a Cartridge Library file to determine the type of test the cartridge is intended to perform. The Cartridge Library holds information that the analyzer needs to run the appropriate scripts and display the correct parameters for each test. Haemonetics periodically provides updates to the Cartridge Library which can be downloaded to your system. The operator should be aware of the problems that could result if these items are stored, installed, or used incorrectly. Storing and handling the analyzer Unpacking the TEG analyzer The TEG analyzer is packaged to reduce the risk of damage during shipment. Remove all polystyrene inserts and carefully remove the TEG analyzer from the box. The power adapter and cables are packaged separately. Note: Save the shipping box and molded polystyrene inserts. If the TEG analyzer needs to be returned for repair or preventive maintenance, it must be shipped in its original packaging in order to avoid damage. Haemonetics will charge for any repairs necessary due to improper packaging. Placement of the TEG analyzer Use the following guidelines to correctly place the TEG analyzer. Place the TEG analyzer on a flat surface such as a table or lab bench. ? Proper operation of the analyzer requires adequate airflow through the cooling fan at the rear of the device. Ensure that the fan is not obstructed by proximity to a wall or other equipment. ?

Isolate the analyzer from all sources of heat (for example, laptops, heaters, or other heat-emitting equipment). ? Make sure that the device is positioned so that it is easy to access the power button and to disconnect the power cord. The TEG analyzer is designed for indoor use only. The operator should wear protective gloves when handling the TEG analyzer. Caution: If the TEG analyzer has been stored at a temperature outside the operating temperature range, allow sufficient time for the analyzer to equilibrate to room temperature before use. Note: See “Specifications” on page 92 for a complete list of environmental conditions in which to store and operate the TEG analyzer. Refer to each product insert for storage and handling instructions. Transporting the analyzer Before transporting the TEG analyzer from one location to another, ensure that all plugs, cords, and cartridges are removed from the device. The analyzer must also be cleaned and disinfected prior to moving the analyzer to a new location, or for return shipment if servicing is necessary. The risk of electrical shock is, therefore, minimal. However, the operator should never remove the analyzer’s covers. Maintenance that requires the removal of these covers remains the responsibility of a Haemonetics-trained technician. Power outlet connection Do not power the device using a power supply other than the one originally supplied by Haemonetics for the TEG analyzer. Always ensure that the power cord is connected to an appropriately grounded power source per your institution’s policy. Caution: Grounding reliability can only be achieved when the equipment is connected to a properly grounded outlet. Caution: Do not unplug the male single-pin connector end of the power cord from the analyzer while leaving the power cord connected to a live power source. Electrical shorting and power supply damage may occur. Bloodborne pathogens Users should adhere to Standard Precautions when handling or using this device.

All parts of the TEG analyzer system should be considered potentially infectious and are capable of transmitting blood-borne pathogens between patients and healthcare professionals. Although the TEG analyzer does not present a significant biohazard risk in itself, the unit is used to analyze human blood, so care must be taken to properly handle, clean, and disinfect the equipment as appropriate. Warning: Special cleaning needs, such as a blood spill, should be dealt with promptly. Follow local standard operating procedure for blood precautions when cleaning up a blood spill or dealing with blood contaminated components. Dispose of all cleaning materials as biohazardous waste. At a minimum, use the following precautions when handling blood and disposing of blood-contaminated material. While operating the TEG analyzer, wear powder-free protective gloves and wash hands immediately after removing the gloves. ? Switch gloves between patients and after completion of testing. ? Wear fluid-resistant clothing. This should only need to be done as required by laboratory protocol and immediately after any blood spill. Precautions must be taken to eliminate or reduce the hazards involved with removing the TEG analyzer from its point of use, transporting it from one place to another, or disposing of the analyzer. If any blood-contaminated material must be returned to Haemonetics for further inspection, see “Product return guidelines” on page 12 for instructions. Proper disposal of biologically contaminated materials Any disposable material used during a procedure is considered to be biologically contaminated and biohazardous. It must be disposed of according to local standard operating procedures for the removal of such material and should not be mixed with non-biohazardous waste. Handling of glass objects Glass objects such as blood collection tubes and Quality Control (QC) vials should be handled with care. Warning: In case of glass breakage, watch for sharp edges.