/GS1 45 0 R /S /URI /TT3 58 0 R 2010, 12(5). crm / / biotronik home monitoring cardiomessenger smart enechnical manual t es manual tcnico fr manuel techniqueh_ ga_ cardiomessenger- smart_ e- mul_ cover. If the monitor is connected to the cellular network in your area there will be a green light or "OK" displayed on your unit. >> 11 0 obj /BS << 3 0 obj google_ad_client: "ca-pub-5568848730124950", /TT3 58 0 R Eradicates time consuming and potentially costly multi-step procedures. 15 0 obj >> /XObject << K190548 FDA clearance. /CS /DeviceRGB /ColorSpace << Every year, more and more patients are receiving ICMs all of which must be actively managed, creating additionalworkloads for everyone involved. Data on file. /Filter /FlateDecode /Contents 56 0 R Caution: Federal law (USA) restricts prescription devices to sale by or on the order of a physician. << /ColorSpace << >> It is also 1.5T and 3.0T full-body MR conditional with no post-injection waiting period limitations. When an AF episode is ongoing during transmission, the monitor transmits both its onset episode and duration. >> 2010, 122(4). /C2_0 53 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. /Rect [90.257 280.24 421.33 294.04] /C2_0 69 0 R /MediaBox [0.0 0.0 612.0 792.0] /Parent 2 0 R 2019, doi: 10.1111/pace.13728. 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. /Rotate 0 /TT0 23 0 R AccuRhythm clinician manual supplements M015316C001 and M015314C001. /Contents [12 0 R 13 0 R 14 0 R 15 0 R 16 0 R 17 0 R 18 0 R 19 0 R] the home monitoring system is comprised of a home monitoring- enabled biotronik pacemaker or defibrillator, cardiomessenger home transmitter, which wirelessly and automatically collects and transmits implant data, and the biotronik home monitoring service center, which allows clinics to review and assess. Alert notifications are not intended to be used as the sole basis for making decisions about patient medical care. /Rect [40.95 36 85.101 45.216] /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] : Berlin-Charlottenburg HRA6501B, Commercial Register No. /BS << Biotronik home monitoring is an award- winning remote monitoring system that provides continuous and automatic wireless remote monitoring of cardiac patient and device status. The permissible positioning zone explained below must always be maintained during MR scans of patients with restricted device systems. /Parent 2 0 R Please check your input. biotronik cardiomessenger ii- llt transmitter for biotronik home monitoring technical manual ( cardio messenger ii- llt, transmitter for biotronik home monitoring) [ biotronik] on amazon. << /TT0 47 0 R Third-party brands are trademarks of their respective owners. Environmental precautions To ensure safe and effective operation, use the device with care to avoid damage to the patient connector from environmental factors that may impair its function. >> /MediaBox [0 0 612 792] /Length 449 The validation study performance and time study results were projected onto 16,301 LINQ II patients to calculate the time saved per year in 200 LINQ II ICM patients. >> 16 0 obj >> AF sensitivity may vary between gross and patient average. 2 0 obj Data availability and alert notifications are subject to Internet connectivity and access, and service availability. Medtronic inductive telemetry uses short-range communication to protect patient information. /S /URI 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. >> /ExtGState << 43 0 R] /GS0 62 0 R var site_url = "https://www.medicaldevices24.com/"; /ExtGState << >> BIOTRONIK BIOMONITOR III, K190548, cleared July 5, 2019 . Nlker G, Mayer J, Boldt L, et al. BIOMONITOR III and BIOMONITOR IIIm can be activated by the patientusing the Remote Assistant III to record cardiac rhythm during symptomatic episodes. The FIT OneStep injection tool provides an ideal pocket to accommodate the device securely and easily. The MR scan with BIOTRONIK systems requires the use of a clinical MRI scanner with a closed bore, cylindrical magnets and a static magnetic field strength of 1.5T or 3T. The isocenter position is an MR condition that describes the permissible scan areas of the patient. It monitors cardiac activity round the clock, day in and day out, with excellent signal fidelity. /TT2 65 0 R PACE. /Contents 72 0 R /Font << It is simple to use, and requires no patient interaction for successful daily data transmissions. endobj Clinical recognition of pure premature ventricular complex-induced cardiomyopathy at presentation. >> the centers for medicare and medicaid services ( cms) ), certified reimbursement coding professionals, other reimbursement experts, and/ or. /Parent 2 0 R << The CareLink mobile application is intended to provide current CareLink network customers access to CareLink network data via a mobile device for their convenience. >> >> See the device manuals for detailed information regarding the implant procedure, indications, contraindications, warnings, precautions, and potential complications/adverse events. By clicking the links below to access the news on our International website, you are leaving this website. If this is not the case please try the monitor closer to a window. /Parent 2 0 R endobj 16Radtke AP, Ousdigian KT, Haddad TD, Koehler JL, Colombowala IK. 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 . 9. /TrimBox [0 0 612 792] /Parent 2 0 R Remote access to full ECGs eliminates the need for manual transmissions 14; . BIOMONITOR III Manual Go to ProMRI SystemCheck Injection Procedure in Less Than One Minute1 >> /CropBox [0 0 612 792] >> Confirm Rx ICM K163407 FDA clearance letter. This website provides worldwide support, except for Japan. 9529 Reveal XT Insertable Cardiac Monitor. /W 0 stream Potential Complications:Potential complications of the Reveal LINQ device include, but are not limited to, device rejection phenomena (including local tissue reaction), device migration, infection, and erosion through the skin. /MediaBox [0 0 612 792] /Pages 2 0 R /A << >> Sorry, the serial number check is currently unavailable. /BleedBox [0 0 612 792] For further information, please call Medtronic at 1-800-929-4043 and/or consult the Medtronic websiteatwww.medtronic.com. }ljxO4!sm4!lO4!l4!l8:7dYAs=8ug]YzYzYzYzYz_s|0s\Cuvt~:r+r8sCq4f>Q'/^dY>MQo+{mw7zyfi Av=&. >> /ProcSet [/PDF /Text /ImageC] 7 0 obj However, the patients particular medical condition may dictate whether or not a subcutaneous, chronically implanted device can be tolerated. /ProcSet [/PDF /Text /ImageC] The unit is battery operated making it easy for patients while travelling, with a battery life of 48 hours. /StructParent 1 10 it is the only system that has been specially approved for the early detection of. GMDN Names and Definitions: Copyright GMDN Agency 2015. BioMonitor 2-AF and Remote Assistant - Mediadatabase BIOTRONIK SE & Co. KG - CRM, Arrhythmia Monitoring, Cardiac Monitor, Accessories, Complete View, Product Family, Gray Background To avoid interference, do not use the patient connector and mobile device within 2 m (6 feet) of other wireless communications equipment. * details on these conditions and requirements can be found in the biotronik promri system technical manual ( www. An MRI scanner's field of view is the area within which imaging data can be obtained. /Parent 2 0 R /URI (http://www.fda.gov/) /TrimBox [0 0 612 792] Overwriting older, more relevant episodes with newer, less relevant data makes classification more difficult. >> /Rotate 0 /Type /Page 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. Performance of an Implantable Cardiac Monitor to Detect Atrial Fibrillation: Results of the DETECT AF Study. Note: A maximum slew rate of 125 T/m/s per axis is valid for Evia, Entovis, Estella and Ecuro models up to and including serial number 66237094. 5178 0 obj <> endobj >> 43 0 R] >> 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 << /Type /Page 9 0 obj 2 today, biotronik home monitoring is available in over 55 countries, optimizing patient management in more than 3, 800 clinics around the world. page 5: about this technical manual about this technical manual about this technical manual user group the cardiomessenger is to be used by patients with a biotronik pacemaker or an implantable cardio- verter- defibrillator ( icd) with the home monitoring function. 7 0 obj 2020. BIOMONITOR III works with BIOTRONIKs fully automated Home Monitoring. /Contents 60 0 R Please enter the country/region where the MRI scan will be performed. /TrimBox [0 0 612 792] 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 /BS << More information (see more) BIOMONITOR III, data on file. /Type /Page Security Maintain adequate physical security of the patient connector to prevent unauthorized use that could lead to harm to patients. >> December 2017;14(12):1864-1870. stream >> hVR8 $[lMQ$d "pD/[_-9 ;eVw[X" 09 (a1%#$($@, !$"B &G?&!z4 >A00vJBjA}:*lu-:GGk+]+YVQ])i[l/tlVJ>}uThtd$ZAe a)\f[Gf65d~bNFtf)wvKH.pjT0+4 _^(604~Vz<18Y Z g`Vp }| 2 s CP0m Ycd>4P@ 6)];TP &1L0J)zgx9r{N29})j/w,a\nD:uLL:YnBLI100* "V_)-|W*^RTW#Xm>\h_F`[ CBA{X )8~f @2pE%]AG?HhIGlD@k(5n^M|r(#"'# 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. See the device manuals for detailed information regarding the implant procedure, indications / intended use, contraindications, warnings, precautions, and potential complications/adverse events. >> /Type /Page /Filter /FlateDecode /StructParent 2 endobj Europace November 1, 2018;20(FI_3):f321-f328. /XObject << /GS0 62 0 R /Type /Pages BIOTRONIK BIOMONITOR IIIm. /Annots [10 0 R 11 0 R] /S /URI /TT1 64 0 R /Im0 67 0 R /C2_1 46 0 R /CS1 [/ICCBased 61 0 R] /Im1 51 0 R /ExtGState << it enables the automatic transmission of a patient s ca. /TT0 63 0 R Electromagnetic Compliance (EMC) testing shows that the patient connector provides reasonable protection against harmful interference and provides EMC immunity in a typical medical installation. 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. >> /W 0 /Type /Action D`"8mk,$K0@YmP~k8N~}i\kb K=8S#2KKTQ+Sb8=+Y4=: + endobj /GS0 44 0 R >> BIOMONITOR III and 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. /Annots [27 0 R 28 0 R 29 0 R 30 0 R 31 0 R 32 0 R 33 0 R 34 0 R 35 0 R 36 0 R Home Monitoring achieves industry leading transmission success rates, along with high levels of patient adherence and satisfaction. cardiomessenger smart heart rate monitor pdf manual download. /XObject << /Type /Page /ProcSet [/PDF /Text] ; page 2: follow- up data overview physician callback signal ( 1) follow- up data transmission ( 2) ready ( cardiomessenger ii) ( 3) battery monitor light ( 4) ready ( charging station) ( 5) data interface ( 6) a view of the rear side of the device can be found on the back cover. There is no guarantee that it will not receive interference or that any particular transmission from this system will be free from interference. Language Title Revision Published Download PDF Change history Printed copy /CS1 [/ICCBased 61 0 R] endobj App Store is a service mark of Apple Inc. 6 Subject to availability by region and as prescribed by a health care professional. endif; ?> BIOTRONIK Remote Assistant III NCC CCAI20LP0360T8 NCC CCAI20LP0360T8 Remote Assistant III (17 kHz) The following details are provided for BIOTRONIK Remote Assistant III from the Taiwanese National Communication Commission type approval licensing registration system. what is home monitoring system? /GS8 23 0 R are permitted for patient monitoring in an mri environment. Home Monitoring not only allows physicians to safely review cardiac function, it also sends alerts about relevant . 2017. Central/Eastern Europe, Middle East & Africa, Electromagnetic Compatibility Guide for Cardiac Devices, Electromagnetic Compatibility for Cardiac Devices, California Transparency in Supply Chains Act, Information About Proposition 65 for California Customers, Digital Millennium Copyright Act (DMCA) Notification, patients with clinical syndromes or situations at increased risk of cardiac arrhythmias, patients who experience transient symptoms such as dizziness, palpitation, syncope, and chest pain that may suggest a cardiac arrhythmia, Patients with clinical syndromes or situations at increased risk of cardiac arrhythmias, Patients who experience transient symptoms such as dizziness, palpitation, syncope, and chest pain, that may suggest a cardiac arrhythmia, patients who experience transient symptoms such as dizziness, palpitation, syncope, and chest pain, that may suggest a cardiac arrhythmia, To verify whether the implanted device has detected a suspected arrhythmia or device related event, To initiate recording of cardiac event data in the implanted device memory, Medtronic Get Connected and Stay Connected, Monitor automatically detects if new data is available, Event notification triggers an actionable alert, Remote access to full ECGs eliminates the need for manual transmissions, Automatic smartphone notifications help patients stay connected, Reduces clinic time spent on patient follow-up. 2019. /TT0 47 0 R >> Monitoring Devices Merlin PCS Help Manual for SJM Confirm, Confirm Rx ICM, Jot Dx Manual. Without complicated set-up procedures, Home Monitoring demonstrates improved patient adherence. /TT3 49 0 R /Font << the device, about the size of a smartphone, keeps pacemaker and implantable cardioverterdefibrillator ( icd) wearers connected to their physician enabling safer, more efficient treatment anywhere in the world. /Count 7 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-. /Length 471 /TT2 49 0 R See the device manual for detailed information regarding the implant procedure, indications, contraindications, warnings, precautions, and potential complications/adverse events. 0 %PDF-1.6 % /GS8 23 0 R Please contact us 4 0 obj Circulation. Biotronik home monitoring is an award- winning remote monitoring system that provides continuous and automatic wireless remote monitoring of cardiac patient and device status. << MRI scans should be performed only in a specified MR environment under specified conditions as described in the Reveal LINQ MRI Technical Manual. Please contact your local BIOTRONIK representative. home monitoring enhances safety for cardiac device patients. You literally just plug it into the power and it is up and running. endobj what is biotronik smart? /CropBox [0.0 0.0 612.0 792.0] >> Designed to minimize patient effort, it sends daily, automatic cardiac device data to the patient device that then forwards the information to the Home Monitoring Service Center (HMSC). However, electronic devices are susceptible to many environmental stresses. endobj /TT1 48 0 R /Type /Group /Contents 68 0 R >> 2019. Lux-Dx ICM K212206 FDA clearance letter. /Font << /TT3 66 0 R endobj Procedural simplicity makes it ideal for in-office settings. /Subtype /Link /Im0 67 0 R endstream endobj startxref The injection procedure allows for several wound closure techniques to be used, including the use of tissue adhesives. /TT4 70 0 R The serial number and product name can be found on: None of the entered data will be stored. /GS0 44 0 R /Length 394 Less information (see less), For greater confidence, the Atrial Fibrillation (AF) and Pause AccuRhythm AI algorithms further enhance the accuracy of the LINQ II ICM data.15-17, LINQ II ICM delivers eight times fewer false positives1,2,7,18. /CS0 [/ICCBased 42 0 R] /GS8 21 0 R The LINQ II insertable cardiac monitoring system is personalized for the patient's lifestyle and customized for the clinician's workflow. /CropBox [0 0 612 792] here AccuRhythm AI algorithms can save clinicians approximately 319 hours of false alert review yearly for every 200 LINQ II ICM patients.21, 84% /CropBox [0 0 612 792] /MediaBox [0.0 0.0 612.0 792.0] kg, and we want you to feel secure when using our web pages. biotronik home monitoring enables physicians to perform therapy management at any time. /CS0 [/ICCBased 60 0 R] It may be used in the home or healthcare facility. /Rotate 0 The patient connector and mobile device may run out of power during the insertion procedure if they are not fully charged. K201865 FDA clearance. what is cardiomessenger smart with biotronik home monitoring? 43 0 R] /Parent 2 0 R Clear P-wave and R-wave visibility supports faster, more confident ECG evaluation. LINQ II Future is Here Video /ColorSpace << 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. /A << << << endobj Performance of an Implantable Cardiac Monitor to Detect Atrial Fibrillation: Results of the DETECT AF Study. /Resources 40 0 R In general, the use of medical devices is only allowed if they are approved. /A << /ProcSet [/PDF /Text /ImageB /ImageC /ImageI] page 1 cardiomessenger ii- llt transmitter for biotronik home monitoring technical manual sbiotronik. We are working quickly to recover this service. >> Performance of an Implantable Cardiac Monitor to Detect Atrial Fibrillation: Results of the DETECT AF Study. hb``d``6d`a` B@q P.p1i@,`yi2*4r 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). %PDF-1.6 % Login with Workspace ONE <B>WARNING:</B> To maintain your login session, make sure that<BR>your browser is configured to accept Cookies. 55 0 obj <>/Filter/FlateDecode/ID[<427DB793BDE2D541B88ED21029101CC0>]/Index[35 38 74 1]/Info 34 0 R/Length 108/Prev 410609/Root 36 0 R/Size 75/Type/XRef/W[1 3 1]>>stream >> /C2_3 62 0 R Neurohormonal, structural, and functional recovery pattern after premature ventricular complex ablation is independent of structural heart disease status in patients with depressed left ventricular ejection fraction: a prospective multicenter study. MRI scans should be performed only in a specified MR environment under specified conditions as described in the device manual. See product manuals for details and troubleshooting instructions. /l%Z1ZHkDOOM/ {Ygp{ 7pv7+r:.n?PYACm?.p^h /Group << 6 0 obj `3$ihfxg'8hd5B_PrV^.Ps'T3=~w4?CIM- {Mk cardiomessenger smart with biotronik home monitoring enhances safety for cardiac device patients new patient device allows for earlier therapy adjustments in heart patients with pacemakers, icds, crt and biomonitor devices. /Tabs /S your IT-Support or your BIOTRONIK contact person. >> >> Update my browser now. Combines pocket creation and ICM injection into a one-step procedure taking only seconds to administer. /TT1 48 0 R /Resources << /StructParents 2 Biotronik, Inc. Jon Brumbaugh Vice President, Regulatory Affairs and Compliance 6024 Jean Road Lake Oswego, Oregon 97035 Re: K190548 Trade/Device Name: BIOMONITOR III, Remote Assistant III Regulation Number: 21 CFR 870.1025 Regulation Name: Arrhythmia Detector and Alarm (Including ST-Segment Measurement and Alarm) Regulatory Class: Class II /CropBox [0.0 0.0 612.0 792.0] - (03:56), Watch this video to learn more about the LINQ II insertable cardiac monitor. /Subtype /Link 1 0 obj /TT2 55 0 R 18 Confirm Rx* ICM DM3500 FDA clearance letter. Why is the selection of a country/region required? Home >> Mobile device access to the internet is required and subject to coverage availability. >> /ArtBox [0 0 612 792] Grant and Donation Requests to BIOTRONIK, Inc. Information Regarding Your Patient Identification Card, Senior Director Microelectronics Engineering. /TT1 48 0 R /ExtGState << >> /Type /Page Do not use the patient connector to communicate with other implanted devices. << >> /Font << /CS0 [/ICCBased 60 0 R] endobj The Patient Assistant activates one or more of the data management features in the Reveal insertable cardiac monitor: Contraindications:There are no known contraindications for the implant of the Reveal XT insertable cardiac monitor. 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. ProMRI Please refer to the technical manual "ProMRI MR condi-tional device systems" for detailed information Without scan exclusion zone and post-operative waiting period 1.5T and 3.0T Tools FIT OneStep injection tool 201mmx24mm (handle) Incision tool 130mmx13mm (handle) Remote Assistant III << Pairing, initialization and data transmission are all automatic, not requiring any active patient involvement. some of the most noteworthy innovations in this eld include biotronik home monitoring, the only fda- and ce- approved remote monitoring system for the early detection of clinically relevant events, and promri technology, allowing implant patients to undergo crucial mri scans. BIOTRONIK BIOMONITOR III technical manual. (8wNi Reveal LINQ Mobile Manager System:The Reveal LINQ Mobile Manager app is intended for programming and interrogating the Reveal LINQ ICM LNQ11. Hip and eye /URI (https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm) /CropBox [0 0 612 792] The patient connector uses Bluetoothtechnology to transmit implantable heart device data to the Reveal LINQ Mobile Manager app for further processing. /CS1 [/Separation /Black [/ICCBased 42 0 R] required expertise in addition to having basic medical knowledge, the user must be thoroughly familiar with the operation of a device system. /Tabs /S >> 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. /StructParents 3 BIOMONITOR III can transmit up to six ECGs to Home Monitoring each day, increasing physicians opportunity to evaluate patient status remotely. J Cardiovasc Electrophysiol. 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. /Type /Page Presented at HRS 2021. The LINQ II ICM is an insertable automatically-activated and patient-activated monitoring system that records subcutaneous ECG and is indicated in adult patients, and in pediatric patients who are at least 2 years old, in the following cases: There are no known contraindications for the insertion of the LINQ II ICM or its accessories. endobj 12 0 obj Isocenter >> /Rect [90.257 307.84 421.33 321.64] Daily verification of data transmissions contributes to an industry leading transmission success rate of 95%. For MRI information in Japan please check the following webpage: www.pro-mri.jp. endstream 2017. 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: /A << /Type /Group TRUST Study, Heart, Lung and Circulation 2009, 18 (s106), 4 Ricci R. P et al HoMASQ study, Europace, 2010, 12 (5). Designed to minimize patient effort, it sends daily, automatic cardiac device data to the patient device that then forwards the information to the Home Monitoring Service Center (HMSC). >> 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. 2 Nlker G, Mayer J, Boldt LH, et al. /Resources << 3 Piorkowski C et al. Contraindications:There are no known contraindications for the implant of the Reveal LINQ ICM or for the Reveal LINQ Mobile Manager system. Artificial Intelligence Enables Dramatic Reduction of False Atrial Fibrillation Alerts from Insertable Cardiac Monitors. endstream endobj 36 0 obj <>/OCGs[56 0 R 57 0 R]>>/OpenAction 37 0 R/Outlines 28 0 R/Pages 33 0 R/Type/Catalog>> endobj 37 0 obj <> endobj 38 0 obj <>/Resources<>/Font<>/ProcSet[/PDF/Text/ImageC]/Properties<>/XObject<>>>/Rotate 0/Thumb 14 0 R/TrimBox[0 0 595.27557373 790.866149902]/Type/Page>> endobj 39 0 obj <>stream reduction in LINQ II false alerts21, 319 /TT4 70 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. You can find detailed information about the requirements, conditions and measures for safely conducting an MRI scan in the. % For further information, please call Medtronic at 1-800-328-2518 and/or consult the Medtronic websiteatwww.medtronic.com. /TT4 59 0 R source exif data [ ] : file type : pdf file type extension : pdf mime type : application/ pdf pdf version : 1. technical manual for the device technical manual for the home monitoring service center ( hmsc) technical manuals for the programmer and the remote assistant iii technical manuals for the user interface technical manuals are either included in hard copy form in the product package or are available in digital form on the internet:. BIOMONITOR IIIm comes ready to inject, pre-loaded into a single piece injection tool for one-step injection. /F 4 Field of view >> All entered data will be deleted when leaving the web page. 4 0 obj /F1 22 0 R ||First European-approved (TV notified body) remote programmable device. >> Please check your input. /Type /Pages Only use the patient connector to communicate with the intended implanted device. 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
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