Copyright 2023 by Shellock R & D Services, Inc. and Frank G. Shellock, Ph.D. All rights reserved. 2715 0 obj <>stream SKU: CD3357-40Q Weight: 3.00 LBS Availability: 4-5 Business days Shipping: Calculated at checkout : Quantity: Share. No use of any Abbott trademark, trade name, or trade dress in this site may be made without the prior written authorization of Abbott, except to identify the product or services of the company. Read our privacy policy to learn more. Copyright 2023 by Shellock R & D Services, Inc. and Frank G. Shellock, Ph.D. All rights reserved. While 1.5T scanners still comprise the majority of MRI installations, 3T scanners may comprise more than half of new units--with some centers having only 3T scanners--since they offer faster scans and higher resolution images. St. Jude bags CE mark for MRI-compatible pacemaker | Fierce Biotech Fierce Pharma Fierce Biotech Fierce Healthcare Fierce Life Sciences Events Research Biotech Medtech CRO Special Reports. Ellipse Implantable Cardioverter Defibrillator (ICD) System, St. Jude Medical. Informa Markets, a trading division of Informa PLC. The MRI pulse sequences are determined by the radiologist and the physicist. Review the general scan requirements. EDORA 8 HF-T/HF-T QP: 1.5 FBS in combination with Solia S 45 lead. Copyright 2023 by Shellock R & D Services, Inc. and Frank G. Shellock, Ph.D. All rights reserved. Boston Scientific ACCOLADE Pacemaker Physician's Technical Manual 359246-001 EN US 2014-05. The CONNECT (Clinical Evaluation of Remote Notification to Reduce Time to Clinical Decision) trial: The value of wireless remote monitoring with automatic clinician alerts. The MRI My Pacemaker platform present at the British Society of Heart Failure 2020 and the Royal College of Physicians AI and Digital Medicine Conference 2021 One of the more time-consuming tasks can be to check whether devices are compatible. Advancements in pacemaker technology have introduced smaller devices, physician-preferred shapes, MR Conditional systems, remote monitoring and increased device longevity. Manufacturer Parent Company (2017) Abbott Laboratories. Abbott offers multiple pacemaker options with unique pacemaker functionality, so you and your team can determine the best pacemaker option for your patients conditions. Theoretically, programming the device to an asynchronous mode should prevent reversion; however, magnet-mode pacing has been seen during scanning despite asynchronous programming and could initiate arrhythmias. 2207-30 CURRENT DR RF MOD. If needed, perform capture and sense and lead impedance tests. The AVEIR VR leadless pacemakerhas an active helical fixation which uses a screw-in mechanism designed for chronic retrieval1,2*, a battery projected to last up to twice as long as current VR leadless pacemakers based on ISO standard settings1,3**and mapping capabilities designed to help reduce the number of repositioning attempts.1,4, The Assurity MRI pacemaker is the worlds smallest, longest-lasting wireless MRI pacemaker.5*** The greater longevity of the Assurity MRI pacemaker reduces the chance of potential device replacement, which means less risk for infection and complications.6, Designed for ease of implant and a smaller incision and pocket size, the Endurity pacemaker can help reduce RV pacing and heart-failure hospitalization with beat-by-beat ventricular support.7. At routine clinic visits this information is retrieved from the pacemaker to guide decisions about your ongoing management. Unless otherwise specified, all product names appearing in this Internet site are trademarks owned by or licensed to Abbott, its subsidiaries or affiliates. These effects are usually temporary. No use of any Abbott trademark, trade name, or trade dress in this site may be made without the prior written authorization of Abbott, except to identify the product or services of the company. Only nondependent patients with mature lead systems (longer than 90 days) were considered. H758582007. Endurity Pacemaker Designed for ease of implant and a smaller incision and pocket size, the Endurity pacemaker can help reduce RV pacing and heart-failure hospitalization with beat-by-beat ventricular support. Not all lead lengths are MR Conditional. Are you a healthcare professional? THE List. + CONVERT MODEL V-195. 3. The device/lead combinations tables below (page 2) lists the MR After device interrogation, prospective patients met with an electrophysiologist to determine whether the patient was pacemaker dependent and the relative need for pacing under baseline conditions. Indications: Implantation is indicated in one or more of the following permanent conditions: syncope, presyncope, fatigue, disorientation due to arrhythmia/bradycardia or any combination of those symptoms. The MRI. St. Jude medical CD3357-40Q UNIFY ASSURA Cardiac Resynchronization Therapy (CRT) Defibrillator. Still, we recommend following these guidelines to stay safe. The information provided here is not intended to provide information to patients and the general public. Select an MRI Device. Persons with known history of allergies to any of the components of this device may suffer an allergic reaction to this device. Is Boston Scientific Ingenio pacemaker MRI compatible? Programming of rate-responsive pacing is contraindicated in patients with intolerance of high sensor-driven rates. Grand Rounds: Cardiac Device Challenges and Innovation, Sex and race disparities found in management of patients with hypertrophic cardiomyopathy in the hospital. P$TqE& 0$gi {Q@W*rN\c`0z}3(?b Lv@ j[ |{Xf`wK3bHED5c@ Rate-Adaptive Pacing may be inappropriate for patients who experience angina or other symptoms of myocardial dysfunction at higher sensor-driven rates. It requires a special lead system, so the generator cannot be simply replaced and connected to in situ intracardiac leads. This webpage is a global search tool of Medtronic, MR-conditional implantable cardiac devices, including pacemakers, ICDs, CRTs, and ICMs. "This new technology allows patients who have heart failure that is challenging to manage to receive more effective therapy and still be able to get an MRI for other medical conditions if needed," Philip Adamson, M.D., medical director of global research and development at St. Jude, said in the statement. 2 06/12/2018 St Jude Medical Inc. Number 8860726. Our manuals contain the latest instructions and information for cardiac physicians, radiologists and MR technologists. Dual-chamber implantable pacemaker, rate-responsive Dual-chamber implantable pacemaker, rate-responsive Dual-chamber implantable pacemaker, rate-responsive Dual-chamber . The Aveir LPs predicate device has chronic retrieval success rate >80% with helix fixation through 7 years regardless of implant duration The Accent MRI pacemaker has been designed and tested for safe performance of a full-body MRI scan, without zone restrictions, using a 1,5 T (Tesla) field-strength MRI scanner. Download the MRI Ready Systems Manual or MRI Ready Leadless System Manual to see examples of checklist screens and get additional details about the checklist. Specific conditions. Each lead needs to be checked for MRI compatibility and individual scan parameters. Safety Info ID#. These devices are sensitive to strong electromagnetic interference (EMI) and can be affected by certain sources of electric or magnetic fields. Immediately following the MRI procedure, follow the instructions in the MRI Ready Systems Manual or MRI Ready Leadless System Manual to revert to the permanently programmed settings. Download latest version here Sphera MRI SureScan. Registered in England and Wales. Patients are supervised by a cardiologist or pacemaker nurse through the procedure. MRI in patients with non-MRI-conditional devices should be considered only if the patient is not pacemaker dependent. Copyright 2023. MAT-2006955 v3.0 | Item is approved for U.S. use. Adobe Reader 6.0 or later is required to view PDF files. 3 LEAD ECG CABLE MODEL EX3001. Contraindications: Dual-chamber pulse generators are contraindicated in patients with an implanted cardioverter-defibrillator. The medical device ASSURITY SR MODEL PM1240 is realized by ST. JUDE MEDICAL INC. Trade name: ASSURITY SR MODEL PM1240: Product Code: PM1240: Manufacturer of the medical device: ST. JUDE MEDICAL INC. Category Name: SINGLE-CHAMBER IMPLANTABLE PACEMAKERS WITH RATE MODULATION SENSOR (SR) Category Code: J01010102: Sign repertoire: Registered: Group . ST. JUDE MEDICAL INC. Category Name: DUAL-CHAMBER IMPLANTABLE PACEMAKERS WITH RATE MODULATION SENSOR (DR) Category Code: J01010302: Sign repertoire: Registered: Group of similar Medical devices: 0: Medical device reference: 0: Type: Medical Device Class: Progressive number assigned to the medical device: 799733: Effective Date: Friday 12 April . Additionally, the first-generation devices are limited to 1.5-tesla scanners. No use of any Abbott trademark, trade name, or trade dress in this site may be made without the prior written authorization of Abbott, except to identify the product or services of the company. Information about the lead (s) and battery function is continuously recorded. I might be wrong about this, but I think you cannot sell a device as MRI compatible in the U.S. without FDA approval. W1SR01. AF Suppression stimulation is not recommended in patients who cannot tolerate high atrial-rate stimulation. EnRhythm MRI SureScan Pacing System, Medtronic, Inc. ARTEN600175956. Lines and paragraphs break automatically. An appropriate Maximum Sensor Rate should be selected based on assessment of the highest stimulation rate tolerated by the patient. Manufacturer comment. M950432A001E 2013-11-15. The medical device ASSURITY MRI PM2272 is realized by ST. JUDE MEDICAL INC. Della stessa categoria di dispositivi medici: ENDURITY MRI PM2172 - PM2172 ENDURITY PM2162 - PM2162 KORA 250 DR - TPM010C ENDURITY PM2152 - PM2152 ENITRA 6 DR - 407153 ENITRA 6 DR-T - 407150 ENTICOS 4 DR - 407155 Legenda Reddy VY, et al. Use this database for arrhythmia, heart failure and structural heart products. Physicians from the Department of Radiology and the electrophysiology group in the Division of Cardiovascular Diseases at Mayo Clinic in Arizona and Minnesota devised a pilot protocol for patients with standard pacemakers in whom MRI was the preferred imaging modality: According to the protocol, the pacemaker is programmed in an asynchronous mode at the intrinsic heart rate plus 20 beats per minute prior to scanning. Please Enter the Pop Up text to be displayed in Pop Up here. Unless otherwise specified, all product and service names appearing in this Internet site are trademarks owned by or licensed to Abbott, its subsidiaries or affiliates. Primary Results on Safety and Efficacy from the LEADLESS II-Phase 2 Worldwide Clinical Trial, JACC: Clinical Electrophysiology, 2021, ISSN 2405-500X, https://doi.org/10.1016/j.jacep.2021.11.002. Proper patient monitoring must be provided during the MRI scan. AF Suppression stimulation is not recommended in patients who cannot tolerate high atrial-rate stimulation. Dual-Chamber Pacing, though not contraindicated for patients with chronic atrial flutter, chronic atrial fibrillation, or silent atria, may provide no benefit beyond that of single-chamber pacing in such patients. Potential Adverse Events: The following are potential complications associated with the use of any pacing system: arrhythmia, heart block, thrombosis, threshold elevation, valve damage, pneumothorax, myopotential sensing, vessel damage, air embolism, body rejection phenomena, cardiac tamponade or perforation, formation of fibrotic tissue/local tissue reaction, inability to interrogate or program a device because of programmer malfunction, infection, interruption of desired device function due to electrical interference, loss of desired pacing and/or sensing due to lead displacement, body reaction at electrode interface or lead malfunction (fracture or damage to insulation), loss of normal device function due to battery failure or component malfunction, device migration, pocket erosion or hematoma, pectoral muscle stimulation, phrenic nerve or diaphragmatic stimulation. THE List. This site is Exclusively Sponsored by BRACCO, Cardiac Pacemakers, Implantable Cardioverter Defibrillators (ICDs), and Cardiac Monitors. (Funded by St. Jud Accessed January 11, 2020. CD1411-36C. This includes the models listed Individual manufacturer allow you to do this and so we have centralised the direct links here: Cardiac MRI is excluded because of potential overheating of the new lead system (second-generation devices currently available in Europe use a lead system that is compatible with cardiac MRI). St. Jude Medical Research Report: Competitive Product Review: Wireless Pacemakers. "All the exams take place on a 1.5-tesla magnet, and the specific absorption rate is limited to 1.5 W/kg for a maximum of 30 minutes," according to Joel P. Felmlee, Ph.D., a radiation physicist at Mayo Clinic in Minnesota. One St. Jude Medical Dr., St. Paul, MN 55117 USA, Tel: 1 651 756 2000 SJM.com St. Jude Medical is now Abbott. Chronotropic competence is defined by the Model of the Cardiac Chronotropic Response to Exercise. The Assurity MRI Cardiac Pacemaker System (Models PM1272, PM2272; St. Jude Medical, Inc., St. Paul, MN) has been designed and tested for performance of an MRI examination using a 1.5-T (Tesla) field-s. More . Pulse oximetry and ECG are monitored. Make a donation. Boston Scientific, 360167-003 EN US 2019-07. Precautions Illustrations are artist's representations only and should not be considered as engineering drawings or photographs. 2708 0 obj <>/Filter/FlateDecode/ID[<0F24CD3BBFCF034381BD972BA11C2BDE><7FEEE39621E4B845877B293CB49ED616>]/Index[2698 18]/Info 2697 0 R/Length 63/Prev 518623/Root 2699 0 R/Size 2716/Type/XRef/W[1 2 1]>>stream CapSure Sense MRI SureScan Models 4074, 4574 Subscribe to our daily e-newsletter. "If pre-scan sequences demonstrate heart rate synchronization to the transmission-receive interval of the radiofrequency coil, the scan is discontinued.". Dual-Chamber Pacing is indicated for those patients exhibiting: sick sinus syndrome, chronic, symptomatic second- and third-degree AV block, recurrent Adams-Stokes syndrome, symptomatic bilateral bundle branch block when tachyarrhythmia and other causes have been ruled out. Once you have completed the checklist, select the Program MRI Settings button to enable MRI Settings. Confirm the MR Conditional components and location of the system. St Jude Medical Inc. PM 1260 ASSURITY + These low voltage (LV) devices are implantable pacemaker pulse generators, inten. St. Jude Medical Accent MRI Pacemaker Rep to Clinician PPT. Safety Topic / Subject. This content does not have an English version. Most pacemakers made since 2000 are MRI-conditional, meaning they are safe for magnetic resonance imaging. Search for arrhythmia, heart failure and structural heart IFUs. Edwards . Prior to use, reference the Instructions for Use, inside the product carton (when available) or online for more detailed information on Indications, Contraindications, Warnings, Precautions and Adverse Events. Boston Scientific. [prod, crx3, samplecontent, publish, crx3tar], https://vascular.abbott.com/,https://mri.merlin.net/,https://www.thelancet.com/,https://www.ahajournals.org/,https://www.onlinejacc.org/,https://jamanetwork.com/,https://www.sciencedirect.com/,https://onlinelibrary.wiley.com/,https://www.cms.gov/,https://www.novitas-solutions.com/,https://event.on24.com/,https://dx.doi.org/,https://www.myloopaccount.com/,https://www.invasivecardiology.com/,https://manuals.sjm.com/,https://www.cardiovascular.abbott, MRI Ready Systems Manual or MRI Ready Leadless System Manual, Interrogate the device with the Merlin PCS Programmer. Copyright 2023 by Shellock R & D Services, Inc. and Frank G. Shellock, Ph.D. All rights reserved. MRI examination of pacemaker-dependent patients should not be performed unless there are highly compelling circumstances and when the benefits clearly outweigh the risks. This site uses cookies. Article Text. Your pacemaker is designed to work properly around most appliances and tools. St. Jude pointed multiple clinical trials and to a 2015 studythat demonstrated that its multiple-point pacing technology may be particularly beneficial in the approximately one third of the total population of CRT patients who do not respond to traditional bi-ventricular pacing therapy. Device Trade Name St. Jude Medical MR Conditional Pacemaker System, consisting of: Assurity MRI Models PM 1272, PM 2272 . Based on the country you select, you can choose the device and lead combination (if applicable) to get scan parameters. Safety Info ID#. This site is Exclusively Sponsored by BRACCO, Assurity MRI Cardiac Pacemaker System, St. Jude Medical, (Models PM1272, PM2272; St. Jude Medical, Inc., St. Paul, MN) has been designed and tested for performance of an MRI examination using a 1.5-T (Tesla) field-s. Indicates a third party trademark, which is property of its respective owner. All pacing abnormalities appear to have been transient and reversible. All rights reserved. You MAY be eligible to have an MRI scan if you are implanted with the Boston Scientific ImageReady MR Conditional pacing system . Feb 2001 - Dec 201716 years 11 months. In this study, device or lead failure did not occur in any patient with a non-MRI-conditional pacemaker or ICD who underwent clinically indicated nonthoracic MRI at 1.5 tesla, was appropriately screened, and had the device reprogrammed in accordance with the prespecified protocol. EDORA 8 SR-T/DR-T: 1.5T FBS + 3T with Thoracic Exclusion Zone in combination with Solia S45 lead. 1998-2023 Mayo Foundation for Medical Education and Research. No. Confirm that no adverse conditions to MR scanning are present. Use is contraindicated in patients with an implanted vena cava filter or mechanical tricuspid valve because of interference between these devices and the delivery system during implantation. On February 29, 2012. the pacemaker unit at the hospital checked the pacemaker and I was told that the lead has to replaced because the ba read more This site uses cookies. 0 By using this site, you consent to the placement of our cookies. Single-Chamber Ventricular Demand Pacing is relatively contraindicated in patients who have demonstrated pacemaker syndrome, have retrograde VA conduction, or suffer a drop in arterial blood pressure with the onset of ventricular pacing. Premature ventricular contractions have been observed, but they have been clinically insignificant. The lead's body has a co-axial design and uses MP35N coils and an Optim outer Presented at the XV International Symposium on Progress in Clinical Pacing, Rome, Italy. "The American College of Radiology recognizes that MRI in patients with pacemakers is never routine and should be conducted only when the case is properly triaged and deemed medically necessary and when alternative radiologic methods have not been diagnostic," according to Robert E. Watson Jr., M.D., Ph.D., a radiologist at Mayo Clinic in Rochester, Minn. "Also, it is stipulated that there is cardiology pacemaker support and careful pacemaker and physiologic monitoring during the MRI, as well as MRI physicist support during imaging.". Number of products: 613. Read our privacy policy to learn more. hb```9@9v284dq;8~Pu|\-En?6}mv'oVl~4hUr %=swV (rPL(xPP:#jcz^J#\.JI+v pPhQ0Kdc:N/&ue\NlI5^(#l*h"?z*::82:8:$":+:::, Download the MRI Ready Systems Manual or MRI Ready Leadless System Manual for details on default settings and how to save modified settings for scanning. When programmed to On, the MRI SureScan feature . MRI Status. %PDF-1.5 % Shutterstock You can have an MRI with a pacemaker, as almost all pacemakers are now considered safe for magnetic resonance imaging. For Cardiac Physicians 1) Confirm MRI readiness It is sold as MRI compatible in the USA but does not have FDA approval for that use. AF Suppression algorithm is indicated for suppression of paroxysmal or persistent atrial fibrillation episodes in patients with one or more of the above pacing indications. For Healthcare Professionals. The following, in addition to the above, are potential complications associated with the use of rate-modulated pacing systems: inappropriate, rapid pacing rates due to sensor failure or to the detection of signals other than patient activity, loss of activity-response due to sensor failure, palpitations with high-rate pacing. By using this site, you consent to the placement of our cookies. However, strong electromagnetic interference (EMI) from some appliances and tools may affect how your pacemaker works. The Quadra Allure with MRI labeling is designed to work with St. Jude's Quartet LV lead, which has four electrodes for different pacing configurations to help manage heart-failure patients. 2 06/12/2018 St Jude Medical Inc. PM1226 ACCENT ST MRI SR RF and PM2222 ACCENT ST These low voltage (LV) devices are implantable pace. Indicates a trademark of the Abbott group of companies. Therefore, MRI in PPM . Rate-Modulated Pacing is indicated for patients with chronotropic incompetence, and for those who would benefit from increased stimulation rates concurrent with physical activity. "As a clinician, I want to offer my patients an advanced cardiac pacing technology that also reserves the option for them to safely undergo a full-body MRI at some point in the future if it's needed," added Prof. Georg Nlker, head of the Electrophysiology, Heart, and Diabetes Center NRW at Ruhr-University of Bochum, Germany. The European approval will allow patients who have the pacemaker to undergo full-body MRI scans of up to 1.5 T. The MRI conditional labelling for the Nanostim leadless pacemaker is expected shortly in the EU. Contraindications: Use of the Aveir Leadless Pacemaker is contraindicated in these cases: Use of any pacemaker is contraindicated in patients with a co-implanted ICD because high-voltage shocks could damage the pacemaker and the pacemaker could reduce shock effectiveness. 2,3. Accessed December 18, 2020. The Amplia MRI CRT-D SureScan Model DTMB1D4/DTMB1D1 and Amplia MRI Quad CRT-D SureScan Model DTMB1QQ/DTMB1Q1, hereafter referred to collectively as the Amplia MRI CRT-D device, is MR Conditional and, as such is designed to allow patients to be safely scanned by an MRI machine when used according to the specified MRI conditions for use. Indications: The Aveir Leadless Pacemaker system is indicated for patients with significant bradycardia and normal sinus rhythm with rare episodes of A-V block or sinus arrest, chronic atrial fibrillation and severe physical disability. The subsequent launch of similar MRI-compatible pacemakers by competitors Boston Scientific and Medtronic undercut St. Jude's bottom line in its cardiac rhythm segment. + VR EPIC MODEL V-196. Mayo Clinic Graduate School of Biomedical Sciences, Mayo Clinic School of Continuous Professional Development, Mayo Clinic School of Graduate Medical Education, Cardiovascular Diseases and Cardiac Surgery, New protocols allow for MRI in selected patients with pacemakers. CAUTION: Do not bring any external control devices, such as the Merlin Patient Care System (PCS) Programmer, SJM MRI Activator handheld device, or Aveir Link Module into the scanner magnet room (Zone IV). THE List. The St. Jude Medical Merlin Patient Care System (PCS) with software model 3330 version 24.0.1 (or greater), a Merlin Antenna (for devices with RF communication), and a telemetry wand constitute the external portion of the ICD and CRT-D systems. ACCENT DR RF MODEL PM2212. Azure MRI SureScan. Adverse Events: Potential complications associated with the use of the Aveir Leadless Pacemaker system are the same as with the use of single chamber pacemakers with active fixation pacing leads including, but not limited to: Cardiac perforation, Cardiac tamponade, Pericardial effusion, Pericarditis, Valve damage and/or regurgitation, Heart failure, Pneumothorax/hemothorax, Cardiac arrhythmias, Diaphragmatic/phrenic nerve stimulation / extra-cardiac stimulation, Palpitations, Hypotension, Syncope, Cerebrovascular accident, Infection, Hypersensitivity reaction to device materials, medications, or direct toxic effect of contrast media on kidney function, Pacemaker syndrome, Inability to interrogate or program the LP due to programmer or LP malfunction, Intermittent or complete loss of pacing and/or sensing due to dislodgement or mechanical malfunction of the LP (non-battery related), Loss of capture or sensing due to embolization or fibrotic tissue response at the electrode, Increased capture threshold, Inappropriate sensor response, Interruption of desired LP function due to electrical interference, either electromyogenic or electromagnetic, Battery malfunction/ premature battery depletion, Device-related complications (Premature deployment, Device dislodgement/embolization of foreign material, Helix distortion), Death. Presented at: HRS 2021; Jul 28-31, 2021; Boston, MA. Article Text. Dont scan the patient if any adverse conditions are present. Indicates a trademark of the Abbott group of companies. ST. JUDE MEDICAL, INC. FDA.report . An appropriate Maximum Sensor Rate should be selected based on assessment of the highest stimulation rate tolerated by the patient. It is required to program the device to MRI Settings as part of the MRI scan workflow. The lead systems are implanted using either transvenous or transthoracic techniques. St. Jude Medicalhas landed the CE Mark for MRI compatibility for its Quadra Allure MP cardiac resynchronization therapy pacemaker. Search for coronary and peripheral disease and valve disease IFUS. Informa PLC's registered office is 5 Howick Place, London SW1P 1WG. Download the MRI Ready Systems Manual or MRI Ready Leadless System Manual to review how data will be handled by each system. Company Name: ST. JUDE MEDICAL, INC. Primary DI Number: 05414734508186 Issuing Agency: GS1 Commercial Distribution End Date: Device Count: 1 Labeler D-U-N-S Number*: 790268031 * Terms of Use Device Description: Cardiac resynchronization device, tiered-therapy cardioverter/defibrillator VVED DDDRV CLOSE Device Characteristics Device Record Status Order a paper copy. Follow the checklist instructions within Merlin PCS Programmer. Single-Chamber Ventricular Demand Pacing is relatively contraindicated in patients who have demonstrated pacemaker syndrome, have retrograde VA conduction or suffer a drop in arterial blood pressure with the onset of ventricular pacing. To look up your patients system, use the Product Search tool to determine whether your patients device and leads (if applicable) are safe for an MRI. Ensure the patient's neurostimulation system is in MRI mode. These devices are considered MR Unsafe. CAUTION: Do not bring any external control devices, such as the Merlin Patient Care System (PCS) Programmer, SJM MRI Activator handheld device, or Aveir Link Module into the scanner magnet room (Zone IV).