Specifically, the patient connector may be affected by electrostatic discharge (ESD). >> /GS1 45 0 R We are working quickly to recover this service. biotronik home monitoring allows follow- up appointments to be catered to you, so that your data is reviewed as necessary, rather than only on a pre- set schedule. /URI (http://www.fda.gov/) - (03:56), Watch this video to learn more about the LINQ II insertable cardiac monitor. /Length 471 /ColorSpace << biotronik also announced the release in japan of its iforia 7 dr- t and vr- t df4 mri- safe implantable cardiac defibrillators, which can use the cardiomessenger home monitoring technology. here /CS /DeviceRGB /C2_2 61 0 R LINQ II Future is Here Video The CareLink mobile application is not replacing the full workstation, but can be used to review patient data when a physician does not have access to a workstation. >> >> Provides daily data trending which may be helpful in determining the need for follow-up. 3 0 obj 9529 Reveal XT Insertable Cardiac Monitor. >> kg, and we want you to feel secure when using our web pages. /GS1 45 0 R /F2 25 0 R /ColorSpace << LINQ II LNQ22 ICM clinician manual. /StructParent 1 /Version /1.4 >> /CS1 [/Separation /Black [/ICCBased 42 0 R] /F 4 RECORDER,EVENT,IMPLANTABLE CARDIAC,(WITH ARRHYTHMIA DETECTION), Storage Environment Atmospheric Pressure: between 70 and 106 KiloPascal, Storage Environment Humidity: between 30 and 95 Percent (%) Relative Humidity, Handling Environment Temperature: between 14 and 113 Degrees Fahrenheit. /ProcSet [/PDF /Text /ImageB /ImageC /ImageI] /XObject << /Resources << Warnings/Precautions:Patients with the Reveal LINQ ICM should avoid sources of diathermy, high sources of radiation, electrosurgical cautery, external defibrillation, lithotripsy, therapeutic ultrasound, and radiofrequency ablation to avoid electrical reset of the device, and/or inappropriate sensing as described in the medical procedure and EMI precautions manual. Home Monitoring achieves industry-leading transmission success rates, along with high levels of patient adherence and satisfaction. Hip and eye - permissible positioning zone. 9 0 obj los resultados publicados recientemente en circulation arrhythmia and electrophysiology confirmaron que biotronik home monitoring proporciona un manejo seguro y econmico de pacientes con marcapasos1, lo que indica que puede reemplazar de manera segura la prctica comn de monitoreo y rutina en consultorio para pacientes con marcapasos. Europace. /Contents 56 0 R See product manuals for details and troubleshooting instructions. 2020. 43 0 R] if you need assistance. >> When an AF episode is ongoing during transmission, the monitor transmits both its onset episode and duration. >> /BleedBox [0 0 612 792] >> BIOMONITOR III and /XObject << Confirm Rx ICM K163407 FDA clearance letter. /TT5 49 0 R /Filter /FlateDecode /ArtBox [0 0 612 792] /Pages 2 0 R /StructParents 0 biotronik home monitoring enables physicians to perform therapy management at any time. >> 43 0 R] The slew rate of the MRI scanner's gradient fields is shown in tesla per meter per second per axis (T/m/s per axis). 7 0 obj /Parent 2 0 R >> /Tabs /S /CS1 [/ICCBased 61 0 R] Contraindications:There are no known contraindications for the implant of the Reveal LINQ ICM or for the Reveal LINQ Mobile Manager system. >> The Patient Assistant activates the data management feature in the Reveal insertable cardiac monitor to initiate recording of cardiac event data in the implanted device memory. The patient connector and mobile device may run out of power during the insertion procedure if they are not fully charged. << /MediaBox [0.0 0.0 612.0 792.0] this transmitter automatically transmits medical and technical information to a mobile device, the cardiomessenger. M974764A001D. << /GS0 62 0 R endif; ?> ICD, pacemaker or cardiac monitor (BIOTRONIK products only). BIOMONITOR III works with BIOTRONIKs fully automatic Home Monitoring. Adapting detection sensitivity based on evidence of irregular sinus arrhythmia to improve atrial fibrillation detection in insertable cardiac monitors. /Im0 67 0 R >> >> If the patient connector does cause harmful interference to other devices or is negatively impacted by other devices, correct the interference by one or more of the following measures: reorient or relocate the patient connector and other devices; increase the separation between the patient connector and other devices by at least two meters (approximately 6 feet); and/ or turn off any interfering equipment. 5 0 obj endobj , the largest, member- driven, healthcare performance improvement company in the united states. /Parent 2 0 R BIOMONITOR III fits a variety of body types. endobj /TT0 23 0 R The device is programmed to an MRI mode before the MR scan. endobj >> if you need assistance. However, the patients particular medical condition may dictate whether or not a subcutaneous, chronically inserted device can be tolerated. << Heart Rhythm. view and download biotronik cardiomessenger smart technical manual online. BIOTRONIK Home Monitoring is a pioneering and award-winning remote cardiac monitoring system. /Resources << var site_url = "https://www.medicaldevices24.com/"; Potential adverse events from the LINQ II ICM include, but are not limited to, device rejection phenomena (including local tissue reaction), device migration, infection, and erosion through the skin. 15 0 obj >> /Group << /TT0 47 0 R /XObject << With an updated browser, you will have a better Medtronic website experience. biotronik home monitoring is a pioneering and award- winning remote cardiac monitoring system. 2017. stream Bluetoothcommunication in the patient connector is encrypted for security. 12 0 obj endstream MRI scans should be performed only in a specified MR environment under specified conditions as described in the device manual. Isocenter 11 0 obj There are no known adverse events associated with the use of any LINQ II ICM wireless accessory. >> /BS << it allows follow- up appointments to be catered to each patient, so that patients are seen when needed, rather than on a pre- set schedule. /Rotate 0 /Length 525 There is no guarantee that it will not receive interference or that any particular transmission from this system will be free from interference. Trade name: REMOTE ASSISTANT: Product Code: 405475: Manufacturer of the medical device: BIOTRONIK SE & CO. KG: Vat Number: 136651322: Category Name: ACTIVE-IMPLANTABLE CARDIAC DEVICES, DIAGNOSTIC - ACCESSORIES: Category Code: J010280: /Type /Action Using the patient connector to communicate with other implanted devices can interfere with those devices, potentially affecting the other implanted devices functionality or therapy delivery. /F 4 Starting from the top of the skull, the permissible positioning zone for the isocenter is at the level of the eyes or the lower edge of the eye socket. It must not be exceeded during the scan. /Contents [14 0 R 15 0 R 16 0 R 17 0 R 18 0 R 19 0 R 20 0 R 21 0 R] Precautions:The AccuRhythm AI ECG classification system may incorrectly adjudicate a true positive episode as an AI false episode, causing that episode to be suppressed in the remote monitoring system. 2 0 obj The medical device REMOTE ASSISTANT is realized by BIOTRONIK SE & CO. KG. /TT5 49 0 R TRUST Study, Heart, Lung and Circulation 2009, 18 (s106), 4 Ricci R. P et al HoMASQ study, Europace, 2010, 12 (5). /CS0 [/ICCBased 60 0 R] All entered data will be deleted when leaving the web page. BIOMONITOR III is theICM that delivers easier and more efficient injection andmonitoring, and our unique BIOvector design providesthe clearest signals for easier evaluation and betterinformed diagnosis. Alert notifications are not intended to be used as the sole basis for making decisions about patient medical care. /Type /Page HKk09F$B`PK!7l|X;j[qz(dsqo^r}wz8;7?mv}Vg(TTA U6M>Mud+JC}&) (rJwvAZOg^ y4]KA'M/8\Lb i+3sQk^I$FkhXE7*lv]+w=U /Parent 2 0 R endobj >> Wireless accessories available for use with LINQ II may experience connectivity or performance issues. Jot Dx ICM K212206 FDA clearance letter. 2020. 2. K201865 FDA clearance. 2 Nlker G, Mayer J, Boldt LH, et al. 2020. /CS1 [/Separation /Black [/ICCBased 42 0 R] /Filter /FlateDecode >> Use of wireless devicesThe patient connector incorporates radiofrequency (RF) communications components which may affect other devices and equipment in the medical environment. /StructParents 3 Healthcare Professionals The scan exclusion zone is determined by the MRI scanner's field of view and the size of the patient. << Mobile device access to the internet is required and subject to coverage availability. No need for unnecessarily complicated delivery tool assemblies. /GS8 21 0 R BIOMONITOR III fits a variety of body types. Sorry, the serial number check is currently unavailable. SRWKU]p3e:A[\V[`;K]>s;%.`46nQRJMzf6#Vh XeXjRj Aid.yA orV\=.I}m_QS7%bM6z~/6F#R]l^zXo{KWH3Xk /Subtype /Link However, electronic devices are susceptible to many environmental stresses. BIOTRONIK BIOMONITOR III technical manual. Cheng YJ, Ousdigian KT, Koehler J, Cho YK, Kloosterman M. Innovative Artificial Intelligence Application Reduces False Pause Alerts while Maintaining Perfect True Pause Sensitivity for Insertable Cardiac Monitors. /S /URI >> /ExtGState << /Contents 72 0 R Warnings and Precautions: The MyCareLink patient monitor must only be used for interrogating compatible Medtronic implantable devices. << endobj 35 0 obj <> endobj @ZvA(thp[x@^P@+70YCT1 5f 4 0 obj /GS7 20 0 R * free* shipping on qualifying offers. Intelligent Memory Management prevents this issue, by retaining the most clinically valid episodes. For further information, please call Medtronic at 1-800-328-2518 and/or consult the Medtronic websiteatwww.medtronic.com. Please see image below. Without complicated set-up procedures, Home Monitoring demonstrates improved patient adherence. endobj Other third party brands are trademarks of their respectiveowners. /Tabs /S /MediaBox [0 0 612 792] >> 5 0 obj If the monitor is connected to the cellular network in your area there will be a green light or "OK" displayed on your unit. /StructParents 4 >> /Contents 49 0 R Do not use the patient connector to communicate with other implanted devices. Please enter the country/region in which the BIOTRONIK product is used. page 7 car di om es s enger _ i i - s_ en. 9539 Reveal XT Patient Assistant:Operation of the Model 9539 Patient Assistant near sources of electromagnetic interference, such as cellular phones, computer monitors, etc., may adversely affect the performance of this device. As the approval process takes a different amount of time in each country, MR conditions and available MR conditional systems may differ from country to country. /Im0 67 0 R Documents Basic Data Expanded Registration Details /Tabs /S /XObject << >> /Type /Group /GS7 22 0 R /XObject << 9529 Reveal XT Insertable Cardiac Monitor. /ArtBox [0 0 612 792] See the device manuals for detailed information regarding the implant procedure, indications / intended use, contraindications, warnings, precautions, and potential complications/adverse events. /CS1 [/ICCBased 61 0 R] >> cardiomessenger smart sends information from the device to the biotronik home monitoring service center over the global system for mobile communication ( gsm) cellular network using wireless rf 2 telemetry and coded data transmission for maximum safety and security. Heart Rhythm. stream /BleedBox [0 0 612 792] BIOMONITOR III, data on file. This website will assist you in determining whether an implanted BIOTRONIK ProMRI system is MR conditional in the country/region where the MRI scan will be performed. Please contact us /Image13 24 0 R CareLink network availability and mobile device accessibility may be unavailable at times due to maintenance or updates, or due to coverage being unavailable in your area. Language Title Revision Published Download PDF Change history Printed copy Low noise also contributes to ECG clarity, which in turn, can lead to easier and quicker rhythm classification. /C2_0 57 0 R /TrimBox [0 0 612 792] dear patient: you have received a biotronik pacemaker or implantable cardioverter- defibrillator ( icd) with home monitoring function. cardiomessenger smart heart rate monitor pdf manual download. BIOMONITOR III has a longevity of 4 years. Additional inputs can be provided with BIOTRONIKs patient app, which has a symptom diary that via direct contact or our Home Monitoring Service Center, keeps patient and physicians fully informed. /F4 48 0 R /Kids [3 0 R 4 0 R 5 0 R 6 0 R 7 0 R 8 0 R 9 0 R] No need for unnecessarily complicated delivery tool assemblies. It has a projected battery life of 4 years and is compatible with Magnetic Resonance Imaging for full-body scans at 1.5 and 3 Tesla. >> /Font << >> will be shown for BIOTRONIK products that have been tested under the conditions of an MR scan and are approved as MR conditional without a scan exclusion zone. For further information, please call Medtronic at (800) 328-2518 (Technical Services), (800) 551-5544 (Patient Services), and/or consult Medtronics website at www.medtronic.com. /TT2 55 0 R monitoring using the home m onitoring function does not serve to replace regular in- office appointments with the physicia n required for othe r medical reasons. home monitoring enhances safety for cardiac device patients. /ProcSet [/PDF /Text /ImageC] /Rotate 0 /S /Transparency LINQ II ICM is ideal for patients experiencing infrequent symptoms that require long-term monitoring or ongoing management. However, there is no guarantee that interference will not occur in a particular installation. BIOMONITOR III works with BIOTRONIKs fully automated Home Monitoring. /F 4 >> Starting from the top of the skull, the permissible positioning zone for the isocenter is at the level of the eyes or the lower edge of the eye socket. Intelligent Memory Management ensures that the detection of both overlapping arrhythmia episodes and patient triggered episodes are stored, with corresponding ECGs always available for evaluation. << << Nlker G, Mayer J, Boldt L, et al. here 2021. /S /URI /Subtype /Link 12 0 obj /TT1 64 0 R /ProcSet [/PDF /Text] /TT0 47 0 R /GS0 44 0 R It has a small can 60% smaller than its predecessor and a flexible antenna, helping to make it comfortable and discreet for patients. /Rect [40.95 36 85.101 45.216] /Parent 2 0 R /C2_0 69 0 R /Rotate 0 You can find detailed information about the requirements, conditions and measures for safely conducting an MRI scan in the. Please enter the device name or order number instead. /BS << /A << hbbd```b``z "XDH`RLE`5[E|H R0Dr 6$d`$4&_ O To ensure the best printing experience, we recommend using the ProMRI SystemCheck on a desktop computer. AF sensitivity may vary between gross and patient average. with home monitoring, the state heart to the patient device, your of your heart' s health and your implant are cardiomessenger ( 2). what is cardiomessenger smart with biotronik home monitoring? In practice, this means that the marker line of the MRI scanner's laser positioning marks must be within this zone. OK is displayed at the top left = connected. Daily verification of data transmissions contributes to an industry leading transmission success rate of 95%. Low noise also contributes to ECG clarity, which in turn can lead to easier and quicker rhythm classification. Why is the selection of a country/region required? /C2_0 46 0 R Please contact your local BIOTRONIK representative. Nlker G, Mayer J, Boldt LH, et al. biotronik se & co. berlin, germany and rome, italy, aug during a scientific talk at the european society of cardiology ( esc) congress, dr. kg / / woermannkehre 1 / / d- 12359 berlin / / germany create date : : 12: biotronik home monitoring manuale 13 13: 18: 51+ 01: 00 modify date : : 12: 13 14: 44: 26+ 01: 00 xmp toolkit : adobe xmp core 5. follow- up supported by home monitoring ca n be used to functionally replac e in-. AF sensitivity may vary between gross and patient average. home monitoring shown to safely and efficiently replace face- to- face follow- ups for pacemaker patients results just published in circulation arrhythmia and electrophysiology confirm that biotronik home monitoring provides safe and cost- effective remote management of pacemaker patients, 1 indicating that it can safely replace the common. 1. >> /Type /Action /Rotate 0 /ExtGState << 9 0 obj >> * details on these conditions and requirements can be found in the biotronik promri system technical manual ( www. The ProMRI Loop Recorder (Biotronik): Full Body MRI at 1.5-T/64-MHz (Biotronik) is MR Conditional and, as such, is designed to allow More . /W 0 For further information, call Medtronic Technical Services at (800) 328-2518 and/or consult Medtronics website at www.medtronic.com. PACE. /Rotate 0 General considerations Users must not rely solely on this information, but must carefully read and observe the ProMRI System Technical Manual for proper use of the implanted system for treatment and determination of MRI compatibility. 2019. Electromagnetic Compliance (EMC) testing shows that the patient connector provides reasonable protection against harmful interference and provides EMC immunity in a typical medical installation. << For further information, please call Medtronic at 1-800-328-2518 and/or consult the Medtronic website atwww.medtronic.com. /BS << An MRI scanner's field of view is the area within which imaging data can be obtained. << >> 10 it is the only system that has been specially approved for the early detection of. /Rotate 0 << Overwriting older, more relevant episodes with newer, less relevant data makes classification more difficult. 5210 0 obj <>/Filter/FlateDecode/ID[<3A0DC8DDBFE34A84B3D7753CE76AFBE9><8F0A54EF42648D4DA9190B0BCFF18DC7>]/Index[5178 220]/Info 5177 0 R/Length 147/Prev 883076/Root 5179 0 R/Size 5398/Type/XRef/W[1 2 1]>>stream /Type /Page reduction in LINQ II false alerts21, 319 Caution: Detailed information about ProMRI can be found in the ProMRI System Technical Manual. Country/region Information Regarding Your Patient ID Card, Team Lead HR Projects, Processes & Reporting. /CropBox [0 0 612 792] Lux-Dx*ICM,Confirm Rx*with SharpSense*technology, Jot Dx*, and BIOMONITOR*III have no published clinical evidence showing AF episode PPV or AF sensitivity. >> it enables the automatic transmission of a patient s ca. /Rect [40.95 36 85.101 45.216] /URI (http://www.fda.gov/) endobj J Am Coll Cardiol. /Contents 41 0 R book page 4 tues day, m ay 6, 1: 11 pm transmits it to the biotronik service center ( 4) as encoded messages via a mobile connection ( 3). /Parent 2 0 R /TT1 48 0 R Products RF interference may affect device performance. Combines pocket creation and ICM injection into a one-step procedure taking only seconds to administer. The website will guide you through the large variety of system-specific MR conditions by requesting information on the implanted device and lead combination. endstream endobj startxref The permissible positioning zone explained below must always be maintained during MR scans of patients with restricted device systems. BIOTRONIK BIOMONITOR III, K190548, cleared July 5, 2019 . /GS0 44 0 R /Type /Page /Type /Page Based on AF episodes 2 minutes and in known AF patients. /ColorSpace << Please check your input. /Type /Page 14 0 obj Contraindications:There are no known contraindications for AccuRhythm AI Models ZA400, ZA410, or ZA420. This website will assist you in determining whether an implanted BIOTRONIK ProMRI system is MR conditional in the country/region where the MRI scan will be performed. Third-party brands are trademarks of their respective owners. 13 0 obj Please enter the country/region where the MRI scan will be performed. /Subtype /Link are permitted for patient monitoring in an mri environment. stream Daily verification of data transmissions contributes to an industry leading transmission success rate of 95%. /BleedBox [0 0 612 792] ]3vuOB1fi&A`$x!2`G9@?0 L /CropBox [0 0 612 792] /Annots [51 0 R] 2017. biotronik home monitoring allows clinics the capability biotronik home monitoring manuale to replace device interrogation during in- office follow- up visits1 and to provide early detection of arrhythmias. your IT-Support or your BIOTRONIK contact person. /TT4 59 0 R /Resources << You literally just plug it into the power and it is up and running. App Store is a service mark of Apple Inc. /CS0 [/ICCBased 60 0 R] Standard text message rates apply. /Annots [10 0 R 11 0 R] >> Unlike bulky Holter monitors, the small device is barely noticeable to the patient. endobj >> >> >> Intended Use:The Medtronic MyCareLink patient monitor and CareLink network are indicated for use in the transfer of patient data from some Medtronic implantable cardiac devices based on physician instructions and as described in the product manual. December 2016;27(12):1403-1410. /StructParents 2 /CropBox [0 0 612 792] 6 Subject to availability by region and as prescribed by a health care professional. Patient data transmitted to CareLink network via MyCareLink Relay or MyCareLink Heart, Clinician-initiated reprogramming via CareLink network, Device settings automatically update without need for an office visit. /TT3 66 0 R var tpl_folder = "https://www.medicaldevices24.com/public/tpl"; BIOMONITOR III is the ICM that delivers both an easy injection procedure and efficient post-procedure monitoring, and our unique BIOvector design provides clear signals for easier evaluation and a better-informed diagnosis. 37 0 R 38 0 R 39 0 R 40 0 R 41 0 R 42 0 R 43 0 R 44 0 R 45 0 R] /Font << /ArtBox [0 0 612 792] 9539 Reveal XT Patient Assistant: . Medtronic inductive telemetry uses short-range communication to protect patient information. Artificial Intelligence Dramatically Reduces Annual False Alerts from Insertable Cardiac Monitors. << Intelligent Memory Management ensures that the detection of both overlapping arrhythmia episodes and patient triggered episodes are stored, and the ECGs are available for evaluation. /S /Transparency << /Im0 50 0 R biotronik is a medical technology company that develops trusted and innovative cardiovascular and endovascular solutions. /GS0 62 0 R /Rect [90.257 307.84 421.33 321.64] This is an instructional video for patients with BIOTRONIK BIOMONITOR devices who use the BIOTRONIK Home Monitoring for remote monitoring.Disclaimer: This vi. Programmer user interface / Programmer printout. we collect, process, and use data in compliance with applicable privacy laws, in particular the eu general data protection regulation ( gdpr), german federal data protection act ( bundesdatenschutzgesetz, bdsg) and the telemedia act ( telemediengesetz, tmg). >> All other brands are trademarks of a Medtronic company. << >> 2017., The exclusive PVC detector may help identify high-risk patients.19,20, BlueSync technology within LINQ II ICM enables secure, wireless communication via Bluetooth Low Energy without compromising device longevity.14. Medtronic Operational Headquarters 710 Medtronic Parkway Minneapolis, MN 55432-5640 USA. BIOMONITOR III is the ICM that delivers easier and more efficient injection and monitoring, and our unique BIOvector design provides the clearest signals for easier evaluation and better informed diagnosis. Ousdigian K, Cheng YJ, Koehler J, et al. /Tabs /S endobj page 1 cardiomessenger ii- llt transmitter for biotronik home monitoring technical manual sbiotronik. >> you can rest easier knowing that biotronik home monitoring manuale you are being monitored and your care team can be condent that they will be notified of clinically relevant device events in between your in- person. /MediaBox [0 0 612 792] << /GS0 44 0 R Warnings/Precautions:Patients with the Reveal XT insertable cardiac monitor should avoid sources of diathermy, high sources of radiation, electrosurgical cautery, external defibrillation, lithotripsy, therapeutic ultrasound, and radiofrequency ablation to avoid electrical reset of the device, and/or inappropriate sensing. /Contents 36 0 R Germany Tel +49 (0) 30 68905-0 Fax +49 (0) 30 6852804 sales@biotronik.com www.biotronik.com enable_page_level_ads: true /Type /Page The injection procedure allows for several wound closure techniques to be used, including the use of tissue adhesives. /Group << BIOTRONIK BIOMONITOR III technical manual. Penela D, Van Huls Van Taxis C, Aguinaga L, et al. /Resources 50 0 R driven by purpose and integrity, biotronik has partnered with hospitals and health systems for more than 50 years, helping to deliver care that saves and improves the lives of millions of patients with heart and blood vessel diseases. >> /Rotate 0 >> /Resources << 16 0 obj gerhard hindricks, leipzig heart center, germany, presented results of a meta- study showing that biotronik home monitoring is associated with a 38 percent reduced risk for all- cause mortality after one ye. >> the transmission power from your device is low and does not impair your health in. /Resources << #K200444 510(k) Summary Page 2 of 4 4. /Contents [52 0 R 53 0 R 54 0 R 55 0 R 56 0 R 57 0 R 58 0 R 59 0 R] /BleedBox [0 0 612 792] /F3 47 0 R Warning: This website provides information on the MRI compatibility of the implanted system. >> /Parent 2 0 R /Rotate 0 Device Descriptions . Hk0Q*dA)4i7KP&POn{pE0>;IF`t Medtronic, Medtronic logo, andEngineering the extraordinary are trademarks of Medtronic. /Tabs /S BIOTRONIK BIOMONITOR III. it sends information on your heart to the transmitter, your cardiomessenger ( 2), usually at night. Disclaimer: A controlled, head-to-head study evaluating the comparative performance of these devices has not been done. Starting from the feet, the permissible positioning zone for the isocenter of the high-frequency coil is at the greater trochanter level. /CS0 [/ICCBased 42 0 R] /TT0 63 0 R This website shows the maximum value for the whole body SAR. << /CS0 [/ICCBased 42 0 R] >> >> /Parent 2 0 R /Group << See the device manuals for detailed information regarding the implant procedure, indications, contraindications, warnings, precautions, and potential complications/adverse events. Indications:The Reveal XT insertable cardiac monitor is an implantable patient-activated and automatically activated monitoring system that records subcutaneous ECG and is indicated in the following cases: The Reveal XT Patient Assistant is intended for unsupervised patient use away from a hospital or clinic. /S /URI This website shows the maximum for the slew rate value, which must not be exceeded during the scan. December 2017;14(12):1864-1870. D`"8mk,$K0@YmP~k8N~}i\kb K=8S#2KKTQ+Sb8=+Y4=: +
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