Premarket Approval (PMA) Coils, Filters, Stents, and Grafts More.
Boston Scientific Sentinol Self-Expanding Nitinol Biliary Stent System with Over-the-Wire Delivery System. If you are not using the MRI Activator, MRI Settings must be disabled by the patient's device management physician or clinician using the Merlin PCS Programmer and Aveir Link Module (if applicable). Our manuals contain the latest instructions and information for cardiac physicians, radiologists and MR technologists. Platinum Chromium Coronary Stent System (Monorail) Device Procode: Applicant's Name and Address: NIQ . "The positive 12-month data from the ORION trial complement our early launch success and market share gains," said Jeff Mirviss, president of Peripheral Interventions at Boston Scientific.
These forward-looking statements are based on our beliefs, assumptions and estimates using information available to us at the time and are not intended to be guarantees of future events or performance. Catalog No. Esophageal Stent, Niti-S & Comvi Model E2423 TaeWoong Medical Co., Ltd., www.stent.net. MR imaging provides excellent spatial . This scientific statement is intended to summarize and clarify issues regarding the safety of MR imaging in patients with cardiovascular devices. All of these factors are difficult or impossible to predict accurately and many of them are beyond our control. of Abbott Medical Japan GK. For more information, please visit: www.bostonscientific.com. PARIS, May 22, 2013 /PRNewswire/ -- Boston Scientific Corporation (NYSE: BSX) reports positive results from two trials evaluating new, innovative drug-eluting stent (DES) technologies, which are emerging treatment options for coronary heart disease. Magnetic Resonance Imaging (MRI) Safety for Boston Scientific Peripheral Products PDF, 272.0 KB.
PDF Summary of Safety and Effectiveness Data (Ssed) Safety Topic / Subject Enterra II Model 37800 Gastric Electrical Stimulation (GES) System . With our stent systems, MRI analyses can now be performed immediately.". Coils, Filters, Stents, and Grafts More. Testing, Training, and Books Implant & Device Testing MAGNETIC RESONANCE SAFETY TESTING SERVICES is a highly experienced MRI-safety testing company that conducts comprehensive evaluations of implants, devices, objects, and materials.
THE List - MRI Safety Introduction II. Boston Scientific is a worldwide developer, manufacturer and marketer of medical devices whose products are used in a broad range of interventional medical specialties. It may be a continuous tube or a mesh structure in tubular form and is available in a variety of lengths and diameters.
AccessGUDID - DEVICE: Ascerta Firm (08714729861775) About Boston ScientificBoston Scientific is a worldwide developer, manufacturer and marketer of medical devices that are used in a broad range of interventional medical specialties. A Boston Scientific Study of the Epic Self-Expanding Nitonol Stent System in the treatment of Atherosclerotic Lesions in Iliac Arteries 0 amputations at 3 years (106 subjects) 89.9% Freedom from TLR at 3 years (143 lesions) ORION US IDE Clinical Trial to demonstrate similar patency across all TASC classifications
It is required to program the device to MRI Settings as part of the MRI scan workflow. Health care professionals and consumers may report adverse reactions or quality problems they experienced using these devices to MedWatch: The FDA Safety Information and Adverse Event Reporting Program using an online form, regular mail, or FAX. The .gov means its official.Federal government websites often end in .gov or .mil. They appreciate the radial force of the stent, which helps allow the artery to stay open, and the flexibility in its design, which helps in deliverability. Catalog No.
PDF Table of Contents - WATCHMAN We disclaim any intention or obligation to publicly update or revise any forward-looking statements to reflect any change in our expectations or in events, conditions or circumstances on which those expectations may be based, or that may affect the likelihood that actual results will differ from those contained in the forward-looking statements. Based on the country you select, you can choose the device and lead combination (if applicable) to get scan parameters. AccessGUDID - Ascerta Firm (08714729861720)- Ureteral Stent. Data from the first human use NG PROMUS Clinical Trial evaluating the safety and effectiveness of the Promus PREMIER Everolimus-Eluting . It was launched in the United States in May of 2012. Forward-looking statements may be identified by words like "anticipate," "expect," "project," "believe," "plan," "estimate," "intend" and similar words.
PDF Summary of Safety and Effectivness (SSED)Template Several of these demonstrated magnetic field interactions. These devices are considered MR Unsafe. hbbd``b` C9E tk`/@PHA,HyM! (,OcEh{[%E#Xl@::9(k]xv# q#fs+[Jb{-$r;EB9 pdRkEdq^(PFG3|'ae1wsv4N5:YBswO[kQC9U0EJ[Tkd/*4s3_SN}W~jj,SPuT-9 )44ZtGtWAO@Fo aP3lqS-P*)v"rj5QEWL!zg8KbORyvm?B'tZ&3D#>7"7Q8&a*$"xmVTeV [@[@.o)BpiyHpV1FIh\w|wD!2N^# U#gb
a]qkz,'@Ri3 Date of Panel Recommendation: None Premarket Approval Application (PMA) Number: P150003/S058 Date of FDA Notice of Approval: August 10, 2020 Indications for Use The Wallstent Venous Endoprosthesis is indicated for improving central venous diameter . Before sharing sensitive information, make sure you're on a federal government site. Boston Scientific Corporation . GMDN Preferred Term Name GMDN Definition; Polymeric ureteral stent A sterile non-bioabsorbable tubular device intended to be implanted in an obstructed ureter (e.g., from stone, stricture, compression, fibrosis, trauma) to maintain luminal patency allowing urine to drain from the renal pelvis to the bladder. Search for arrhythmia, heart failure and structural heart IFUs.
Class 3 Device Recall Sentinol Nitinol Biliary Stent System A tracking/verification form is asked to be returned to Boston Scientific and arrangements will be made for retuning the affected product.
Download the MRI Ready Systems Manual or MRI Ready Leadless System Manual to review how data will be handled by each system. DVAz~U|OH_P&xuN)Z6:U<0GI+LQj%]mr2&4SCjyWlQq0H[-2vmu5*Q]zp`MocdS.I>^fp~DEBdo(t
1.5 . We recommend that you download and review the most current version any time a patient with an Abbott product needs an MRI. Boston Scientific Corporation Customer Service: 8882721001 www.bostonscientific.com Page 1 of 12 PI86716AG Magnetic Resonance Imaging (MRI) Safety for Boston Scientific Products Table of Contents 1. MRI safety testing has shown that the REBEL Stent is MR Conditional and that "The FDA approval of the timing on MRI exams is a significant development for interventional cardiologists and their patients," said Paul LaViolette, Boston Scientific Chief Operating Officer. f@
THE List - MRI Safety Dry Pad 9 x 9 with Silver Antimicrobial Agent. The positive data support the Boston Scientific goal of delivering products designed to reduce the need for reinterventions and help lower overall healthcare costs. The Notice described the issue, identified affected product and asked that the use of affected product be discontinued and affected units be segregated. Abbotts MRI-Ready High Voltage Device Setup for Gallant and Entrant ICD and CRT-Ds (11:45). The ORION clinical data was used to support application for U.S. Food and Drug Administration approval of the Epic Stent System. Dont scan the patient if any adverse conditions are present. Note: Boston Scientific is not responsible for the correct use of codes on submitted claims; this informationdoes not constitute reimbursement or legal advice. Boston Scientific 2 Agenda I.
PDF Summary of Safety and Effectiveness 0.3. Safe More. 2022 Boston Scientific Corporation or its affiliates. 3: Conditional 6 . Boston Scientific performed rigorous laboratory testing to demonstrate MRI compatibility. Coronary data supports safety of paclitaxel and ELUVIA DES IV. Indicates a trademark of the Abbott group of companies.
AccessGUDID - DEVICE: Tria Soft (08714729959915) The product, pouch label and carton label are all correct and the correct DFU is in the package. This site uses cookies. As the stent is exposed to body temperature it expands to appose the duct wall. %%EOF
This press release contains forward-looking statements within the meaning of Section 27A of the Securities Act of 1933 and Section 21E of the Securities Exchange Act of 1934. Based on the country you select, you can choose the device and lead combination (if applicable) to get scan parameters. The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely. endstream
endobj
startxref
Use this database for coronary intervention, peripheral intervention and valve repair products. The Express Coronary Stent System was granted approval by Boston Scientific's notified body (TUV Rheinland) to permit CE marking June 18, 2001. HWnFC=ji6n
9/~\:\$$rxnsU,)Ielo((a,$4bY?W7)MoQEHk1s-;]zXJ$G=0.F4VJYwS|U9VOU@n0ZL26w~+y38.$qW|%-zu'2g:,IwA28nvnP
R%ivTpks5>/m5p)H,!HIsqz
9x?pFH=@q}+[|Gd $Xp7lXcV5ZID?vM1V]kM).? This site is Exclusively Sponsored by BRACCO. One lot of one catalog number of the Sentinol Nitinol Biliary Stent System may have been packaged in a Sentinol nitinol Vascular outer carton. endstream
endobj
60 0 obj
<>>>/Filter/Standard/Length 128/O(v~aIgInj rM)/P -1340/R 4/StmF/StdCF/StrF/StdCF/U( ey,62_ )/V 4>>
endobj
61 0 obj
<>>>
endobj
62 0 obj
<>
endobj
63 0 obj
<>/ExtGState<>/Font<>/ProcSet[/PDF/Text]/Properties<>/Shading<>/XObject<>>>/Rotate 0/TrimBox[24.0 24.0 619.276 865.89]/Type/Page>>
endobj
64 0 obj
<>stream
Fortunately, the devices that exhibited po . Follow the checklist instructions within Merlin PCS Programmer. Boston Scientific, www.bostonscientific.com, Neuroform Atlas Stent Non-clinical testing and analysis have demonstrated that the Neuroform Atlas Stent is MR Conditional alone, or when overlapped with a second stent, and adjacent to a Stryker Neur, AAA Endograft Ovation Ovation Abdominal Stent Graft System TriVascular2, Inc. Santa Rosa, CA, Abre StentMedtronic, Inc., www.Medtronic.com/MRI, Absolute .035 Biliary Self-Expanding StentAbbott Vascular, www.abbottvascular.com, ABSOLUTE 0.35 Biliary Self Expanding Stent System Guidant http://www.guidant.com/ifu/, Absolute Biliary StentAbbott Vascularwww.abbottvascular.com, Absolute Pro .035 Biliary Self-Expanding StentAbbott Vascular, www.abbottvascular.com, Absolute Pro Peripheral Stent Abbott Vascular www.Abbott.com, Absolute Pro Stent Nickel titanium with nickel titanium platinum markers 8-mm x 120-mm Single version Abbott Vascular Santa Clara, CA, Absolute Pro Stent Nickel titanium with nickel titanium platinum markers 8-mm x 348-mm three overlapped version Abbott Vascular Santa Clara, CA, ABSOLUTE Biliary Self-Expanding Stent System Nitinol coils, filters, stents Guidant Endovascular Solutions Santa Clara, CA, Absorb Bioresorbable Vascular Scaffold (BVS) SystemAbbott Vascular, www.abbottvascular.com, Absorb GT1 Bioresorbable Vascular Scaffold (BVS) SystemAbbott Vascular,www.abbottvascular.com, Acculink Carotid StentAbbott Vascularwww.abbottvascular.com, ACCULINK Carotid StentGuidanthttp://www.guidant.com/ifu/, ACS MULTI-LINK Coronary StentAbbott Vascularwww.abbottvascular.com, ACS MULTI-LINK DUET Coronary StentAbbott Vascularwww.abbottvascular.com. If the stent migrates to the heart, it could cause life-threatening injury. Boston Scientific is dedicated to transforming lives through innovative medical solutions that improve the health of patients around the world. Device setup, user manuals and troubleshooting, The Boston Scientific Epic Stent Continues to Demonstrate Positive Clinical Outcomes for Patients with Iliac Artery Disease, Twelve-Month Data Presented at TCT 2012 Support Safety and Efficacy of Epic Stent in Iliac Stenting, Lab Agent - Restock Products For Your Practice, Bladder leakage and pelvic organ prolapse, Enteral feeding tube and esophageal stent device support, Cardiac Resynchronization Therapy (CRT) device support, Peripheral Artery and Vein interventions device support, Transcatheter Aortic Valve Replacement device support, Spinal Cord Stimulator (SCS) systems device support, EDUCARE Medical Education and Training Courses, ADVANTICS Innovative Healthcare Solutions, Do not sell or share my personal information. Shellock R & D Services, Inc. email: Frank.ShellockREMOVE@MRIsafety.com. The Sentinol Nitinol Stent System is comprised of two components: the implantable . The TAXUS Express2 and Express2 systems were shown to be MRI safe at a high level of magnetic field strengths with minimal effect on temperature rise and drug release. 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. Use this database for arrhythmia, heart failure and structural heart products. The revised Express2 bare-metal stent DFU will be available shortly. Marlborough, MA 01752-1566 . 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. All rights reserved. Unless otherwise specified, all product names appearing in this Internet site are trademarks owned by or licensed to Abbott, its subsidiaries or affiliates.
Are you a healthcare professional? Boston Scientific is recalling the VICI SDS and RDS VENOUS STENT Systems after reports indicate that the stents may migrate or move from where they are initially implanted. Cautionary Statement Regarding Forward-Looking Statements. You can search by product, model number, category or family. A non-bioabsorbable tubular device intended to be implanted in the common and/or external iliac artery(ies) to maintain arterial patency and luminal diameter in patients with symptomatic atherosclerotic disease. Patients experienced significant clinical improvement from baseline to twelve months based on feedback from validated questionnaires evaluating walking distance, speed and stair climbing. Sterile. Physicians interested in reviewing a complete copy of the revised TAXUS Express2 stent DFU may obtain a copy from the TAXUS website at www.taxus-stent.com. Download the MRI Ready Systems Manual or MRI Ready Leadless System Manual to review a list of adverse conditions and effects. 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. Reproduced with Permission from the GMDN Agency. As a result, readers are cautioned not to place undue reliance on any of our forward-looking statements. 5-year data for. Factors that may cause such differences include, among other things: future economic, competitive, reimbursement and regulatory conditions; new product introductions; demographic trends; intellectual property; litigation; financial market conditions; and future business decisions made by us and our competitors. Applicant's Name and Address: Boston Scientific Scimed Inc. One Scimed Place Maple Grove MN 55311-1566 PMA Number: P980033 Date of Notice of Approval to the Applicant: Novermber 16, 2001 2. Boston Scientific, www.bostonscientific.com . 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. Stent delivery system (SDS): A system that delivers a biliary stent to a target site within the bile duct and then deploys the stent. There have been 17 complaints and reported injuries related to this issue.