Icast stent instructions for use Ulooloo

Icast stent instructions for use

iCast Balloon Expandable Covered Stent DAIC † These calculations assume the minimum 30 mm overlap between the bifurcated stent graft and the contralateral iliac limb per the Endurant II Stent Graft System Instructions For Use. When using the 124 mm length bifurcated stent graft, subtract 10 mm from …

Atrium iCast Covered Stent bmctoday.net

Adherence to EVAR Device Instructions for Use (IFU. 29/03/2016 · Stents available for use in the aortoiliac arteries can be divided into balloon-expandable stents, self-expanding stents, and covered stents. Although significant data exist for each stent type, most clinical studies have included patients with relatively less-complex disease. In addition, little comparative data exist between stent types., Use caution when advancing the endovascular system through tortuous or difficult anatomy. This device has not been tested for use in overlapped conditions with stents or covered stents from other manufacturers. Please consult package insert for more detailed safety information and instructions for use..

29/03/2009 · Table 3 is a list of commercially available covered stents (used for peripheral indications) in the U.S. Aortic Endografts. The advances in the development of intravascular stents made possible the construction and approval of the currently available endovascular grafts for the treatment of abdominal and thoracic aortic pathology. Endovascular treatment of TransAtlantic Inter-Society Consensus II (TASC) D aortoiliac occlusive lesions remains a challenge, but a valuable treatment option in poor surgical candidates. We present our operative technique and midterm results in treating TASC D aortoiliac occlusive disease using unibody bifurcated endografts.

The Omnilink Elite Stent System is intended to perform as a system.The stent should not be removed for use in conjunction with other dilatation catheters, nor should the delivery system be used in conjunction with other stents; Refer to the instructions for use supplied with any interventional devices to be used in conjunction with the Omnilink Use caution when advancing the endovascular system through tortuous or difficult anatomy. This device has not been tested for use in overlapped conditions with stents or covered stents from other manufacturers. Please consult package insert for more detailed safety information and instructions for use.

The stent's patented design balances strength and flexibility for proven patency as found in the VISIBILITY ILIAC study. Radiopaque markers on the stent ensure precise placement. Deliver over an 0.035" guidewire for use in the common or external iliac arteries or in the biliary system. Before withdrawing the stent graft delivery system, visually confirm complete balloon deflation by fluoroscopy to avoid guiding catheter movement into the vessel and subsequent arterial damage. Carefully read all instructions prior to use. Observe all warnings and precautions noted throughout these instructions. Failure to do so may result in

The stent's patented design balances strength and flexibility for proven patency as found in the VISIBILITY ILIAC study. Radiopaque markers on the stent ensure precise placement. Deliver over an 0.035" guidewire for use in the common or external iliac arteries or in the biliary system. Use caution when advancing the endovascular system through tortuous or difficult anatomy. This device has not been tested for use in overlapped conditions with stents or covered stents from other manufacturers. Please consult package insert for more detailed safety information and instructions for use.

atrium iCAST™ Balloon expandable Covered Stent. Atrium’s iCAST™ balloon expandable covered stent is FDA 510(k) cleared for the treatment of tracheobronchial strictures. The iCAST covered stent provides deployment accuracy due to its precision stent delivery platform and its low foreshortening design. The iCAST stent is crafted using Atrium’s PTFE encapsulation technology and a one-step deployment … 09/11/2019 · Self-expanding polyethylene terephthalate and polytetrafluoroethylene (PTFE)-covered stents have been shown to decrease the need for repeat …

that Cordis offers products for every use or procedure discussed and the FDA-cleared or approved labeling for all products may not be consistent with the information in this guide. As always, please refer to the product’s instructions for use or package insert for a complete description of indications and contraindications for any medical Patients with benign and malignant central airway obstruction suffer from disabling dyspnea, obstructive pneumonia, and impending suffocation. Therapeutic bronchoscopy provides immediate and gratifying palliation. Airway stenting is the principal modality used to manage intrinsic tracheobronchial pathology and extrinsic airway compression. This report provides the details of the indications

• Prior to implantation of the MERIT ENDOTEK AEROmini Tracheobronchial Stent System, the physician should refer to the Sizing Table (Table 1 & 2) and read the Instructions for Use. • When used in the treatment of stenotic or obstructive lesions, placement of the stent should immediately follow the opening of the airway by 9. Rogers C, Edelman EA Non-GLP Study of biologic responses to uncoated and PTFE coated steel stents in rabbit iliac arteries. MIT iCAST IH Study, July 16, 1997. 10. Sabri et al. Outcomes of covered kissing stent placement compared with bare metal stent placement in the treatment of atherosclerotic occlusive disease at the aortic bifurcation.

The stent's patented design balances strength and flexibility for proven patency as found in the VISIBILITY ILIAC study. Radiopaque markers on the stent ensure precise placement. Deliver over an 0.035" guidewire for use in the common or external iliac arteries or in the biliary system. The Ultraflex Tracheobronchial Stent System is provided sterile in both covered and uncovered versions and is indicated for use in the treatment of tracheobronchial strictures produced by …

Prospective, multicenter, non-randomized, single-arm registry to evaluate the safety and effectiveness of the iCAST Covered Stent System in the treatment of patients with symptomatic claudication or rest pain and angiographic confirmation of de novo or restenotic lesions in the common and/or external iliac artery. Fenestrated stent graft system. device descriPtioN The Zenith Fenestrated stent graft has been approved to treat patients with short-necked abdominal aortic aneurysms that are ≥ 4 mm in length and those who do not meet the proposed anatomical criteria for the use of infrarenal stent grafts. The device consists of a …

Techniques in Endovascular Aneurysm Repair

Icast stent instructions for use

Endovascular treatment of TransAtlantic Inter-Society. Widely used Iliac stent, well-known for its outstanding com-pression resistance. Its Tandem Architecture has been designed to provide excellent conformability to vessel anatomies. The outstanding compression resistance of the EXPRESS Vascular LD Stent makes it an excellent choice for bifurcations or resistant lesions when strength is critical. The Express Vascular LD Iliac Pre-mounted Stent, Prospective, multicenter, non-randomized, single-arm registry to evaluate the safety and effectiveness of the iCAST Covered Stent System in the treatment of patients with symptomatic claudication or rest pain and angiographic confirmation of de novo or restenotic lesions in the common and/or external iliac artery..

Safety Information AFX - Endologix. 9. Rogers C, Edelman EA Non-GLP Study of biologic responses to uncoated and PTFE coated steel stents in rabbit iliac arteries. MIT iCAST IH Study, July 16, 1997. 10. Sabri et al. Outcomes of covered kissing stent placement compared with bare metal stent placement in the treatment of atherosclerotic occlusive disease at the aortic bifurcation., The iCAST covered stent provides deployment accuracy due to its precision stent delivery platform and its low foreshortening design. The iCAST stent is crafted using Atrium’s PTFE encapsulation technology and a one-step deployment technique for precise, accurate deployment..

Pivotal Study of a Next-Generation Balloon-Expandable

Icast stent instructions for use

Adherence to EVAR Device Instructions for Use (IFU. Instructions For Use Finder; Zilver® PTX® Drug-Eluting Peripheral Stent Specifications Videos Documents Images. Handle of the Zilver PTX delivery system Zilver PTX Drug-Eluting Peripheral Stent. Indicated for improving luminal diameter for the treatment of de novo or restenotic symptomatic lesions in native vascular disease of the above-the-knee femoropopliteal arteries having reference https://en.wikipedia.org/wiki/Stent Prospective, multicenter, non-randomized, single-arm registry to evaluate the safety and effectiveness of the iCAST Covered Stent System in the treatment of patients with symptomatic claudication or rest pain and angiographic confirmation of de novo or restenotic lesions in the common and/or external iliac artery..

Icast stent instructions for use


Specific follow-up guidelines are described in the Instructions For Use under, Imaging Guidelines and Post-Operative Follow-up. After endovascular graft placement, patients should be regularly monitored for perigraft flow, aneurysm growth or changes in the structure or position of the endovascular graft. † These calculations assume the minimum 30 mm overlap between the bifurcated stent graft and the contralateral iliac limb per the Endurant II Stent Graft System Instructions For Use. When using the 124 mm length bifurcated stent graft, subtract 10 mm from …

25/10/2011 · Most often, the internal iliac artery must be covered with this method, and pelvic ischemia can result. Endograft limbs may be used, but the Gore Viabahn, Bard Fluency plus vascular stent graft, and Atrium iCAST covered stents could also be used off label for this technique (Figure 1). While both the Viabahn and Fluency stents are self Patients with benign and malignant central airway obstruction suffer from disabling dyspnea, obstructive pneumonia, and impending suffocation. Therapeutic bronchoscopy provides immediate and gratifying palliation. Airway stenting is the principal modality used to manage intrinsic tracheobronchial pathology and extrinsic airway compression. This report provides the details of the indications

Use of a PTFE-covered BE stent (iCast Covered Stent, Atrium Medical Corp, Hudson, NH; or Graft Master Stent, Abbott Vascular Devices, Santa Clara, CA) is another potential method to treat renal ISR, although neither device is approved for this indication, nor is there evidence to support their use. Summary. Prospective, multicenter, non-randomized, single-arm registry to evaluate the safety and effectiveness of the iCAST Covered Stent System in the treatment of patients with symptomatic claudication or rest pain and angiographic confirmation of de novo or restenotic lesions in the common and/or external iliac artery.

stents is a safe and effective therapeutic option when such aneurysms are limited to the proximal or midportion of the renal artery. A brachial artery approach is often required in such cases due to significant renal artery tor-tuosity or downward angulation. Table. Select demographics and outcomes by instructions for use (IFU) status Variable Specific follow-up guidelines are described in the Instructions For Use under, Imaging Guidelines and Post-Operative Follow-up. After endovascular graft placement, patients should be regularly monitored for perigraft flow, aneurysm growth or changes in the structure or position of the endovascular graft.

Use of a PTFE-covered BE stent (iCast Covered Stent, Atrium Medical Corp, Hudson, NH; or Graft Master Stent, Abbott Vascular Devices, Santa Clara, CA) is another potential method to treat renal ISR, although neither device is approved for this indication, nor is there evidence to support their use. 29/03/2016 · Stents available for use in the aortoiliac arteries can be divided into balloon-expandable stents, self-expanding stents, and covered stents. Although significant data exist for each stent type, most clinical studies have included patients with relatively less-complex disease. In addition, little comparative data exist between stent types.

Use caution when advancing the endovascular system through tortuous or difficult anatomy. This device has not been tested for use in overlapped conditions with stents or covered stents from other manufacturers. Please consult package insert for more detailed safety information and instructions for use. Specific follow-up guidelines are described in the Instructions For Use under, Imaging Guidelines and Post-Operative Follow-up. After endovascular graft placement, patients should be regularly monitored for perigraft flow, aneurysm growth or changes in the structure or position of the endovascular graft.

• Prior to implantation of the MERIT ENDOTEK AEROmini Tracheobronchial Stent System, the physician should refer to the Sizing Table (Table 1 & 2) and read the Instructions for Use. • When used in the treatment of stenotic or obstructive lesions, placement of the stent should immediately follow the opening of the airway by All iCast stents are 0.035-inch guidewire compatible and are mounted on a 5-F catheter shaft size with available lengths of 80 and 120 cm. Devices are compatible with either a 6- or 7-F introducer sheath. The iCast is currently approved for the treatment of tracheobronchial strictures.

Patients with benign and malignant central airway obstruction suffer from disabling dyspnea, obstructive pneumonia, and impending suffocation. Therapeutic bronchoscopy provides immediate and gratifying palliation. Airway stenting is the principal modality used to manage intrinsic tracheobronchial pathology and extrinsic airway compression. This report provides the details of the indications The Ultraflex Tracheobronchial Stent System is provided sterile in both covered and uncovered versions and is indicated for use in the treatment of tracheobronchial strictures produced by …

The stent is indicated for use in occlusions, lesions at high risk for abrupt closure or threatened closure following percutaneous transluminal angioplasty (PTA) or lesions believed to be at high risk of restenosis following PTA in the common iliac, external iliac, or subclavian arteries. The stent is also intended as a palliative treatment of Fenestrated stent graft system. device descriPtioN The Zenith Fenestrated stent graft has been approved to treat patients with short-necked abdominal aortic aneurysms that are ≥ 4 mm in length and those who do not meet the proposed anatomical criteria for the use of infrarenal stent grafts. The device consists of a …

Atrium Interventional Surgery iCASTв„ў Covered Stent

Icast stent instructions for use

GOREВ® VIABAHNВ® Endoprosthesis Gore Medical. Endovascular treatment of TransAtlantic Inter-Society Consensus II (TASC) D aortoiliac occlusive lesions remains a challenge, but a valuable treatment option in poor surgical candidates. We present our operative technique and midterm results in treating TASC D aortoiliac occlusive disease using unibody bifurcated endografts., Prospective, multicenter, non-randomized, single-arm registry to evaluate the safety and effectiveness of the iCAST Covered Stent System in the treatment of patients with symptomatic claudication or rest pain and angiographic confirmation of de novo or restenotic lesions in the common and/or external iliac artery..

FLEXIVE bsci-prod2-origin.adobecqms.net

Atrium iCast Covered Stent bmctoday.net. Use caution when advancing the endovascular system through tortuous or difficult anatomy. This device has not been tested for use in overlapped conditions with stents or covered stents from other manufacturers. Please consult package insert for more detailed safety information and instructions for use., 25/10/2011 · Most often, the internal iliac artery must be covered with this method, and pelvic ischemia can result. Endograft limbs may be used, but the Gore Viabahn, Bard Fluency plus vascular stent graft, and Atrium iCAST covered stents could also be used off label for this technique (Figure 1). While both the Viabahn and Fluency stents are self.

Please consult Instructions for Use for product indications for use, contraindications, warnings, precautions, complications, adverse events and detailed safety information. BPV/BPAL/0916/0051a 0 All iCast stents are 0.035-inch guidewire compatible and are mounted on a 5-F catheter shaft size with available lengths of 80 and 120 cm. Devices are compatible with either a 6- or 7-F introducer sheath. The iCast is currently approved for the treatment of tracheobronchial strictures.

9. Rogers C, Edelman EA Non-GLP Study of biologic responses to uncoated and PTFE coated steel stents in rabbit iliac arteries. MIT iCAST IH Study, July 16, 1997. 10. Sabri et al. Outcomes of covered kissing stent placement compared with bare metal stent placement in the treatment of atherosclerotic occlusive disease at the aortic bifurcation. The stent is indicated for use in occlusions, lesions at high risk for abrupt closure or threatened closure following percutaneous transluminal angioplasty (PTA) or lesions believed to be at high risk of restenosis following PTA in the common iliac, external iliac, or subclavian arteries. The stent is also intended as a palliative treatment of

The stent system is compatible with 0.035-inch guide wires and 6-F (stents with diameters of 5 mm and 6 mm in lengths of 16 mm and 22 mm), 7-F (stents with diameters of 5–10 mm), and 9-F (stents with diameter of 12 mm) introducer sheaths. sue. Atrium comments that iCast has the lowest crossing profile com-pared to other commercially available stents, providing for a more effi-cient delivery. For 5-mm to 10-mm sizes, iCast is 7-F compatible; the 12-mm version is 8-F compatible. Atrium iCast Covered Stent GE Healthcare (Milwaukee, WI) has launched the

Please consult Instructions for Use for product indications for use, contraindications, warnings, precautions, complications, adverse events and detailed safety information. BPV/BPAL/0916/0051a 0 This is not recommended as the proximal end of the stent may catch the edge of the introducer sheath, thus dislodging the stent. The instructions for use provided with the catheter system also recommends not to attempt to pull the device back through the introducer sheath, but to pull the stent and sheath together out of the pt as a unit. The

sue. Atrium comments that iCast has the lowest crossing profile com-pared to other commercially available stents, providing for a more effi-cient delivery. For 5-mm to 10-mm sizes, iCast is 7-F compatible; the 12-mm version is 8-F compatible. Atrium iCast Covered Stent GE Healthcare (Milwaukee, WI) has launched the Stents for Aorto-iliac Occlusive Disease: New Trial Data makes for an Interesting Comparison 3rd December 2016 Balloon Expandable Covered Stents in Aorto-iliac Occlusive Disease: Suddenly a Crowded Space Andrew Holden Auckland, New Zealand L INC 2018. D is c lo s u r e S p e a k e r n a m e : A n d r e w H o ld e n..... I h a v e th e fo llo w in g p o te n tia l c o n flic ts o f in te r e s

For more than 15 years, by touching over 500,000 lives, our Advanta V12 balloon expandable covered stent has been trusted by physicians for its ease of use and proven, reliable outcomes. Designed with a unique PTFE covering technology, Advanta V12 inspires confidence with high patency and low reintervention rates. Use of a PTFE-covered BE stent (iCast Covered Stent, Atrium Medical Corp, Hudson, NH; or Graft Master Stent, Abbott Vascular Devices, Santa Clara, CA) is another potential method to treat renal ISR, although neither device is approved for this indication, nor is there evidence to support their use.

Before withdrawing the stent graft delivery system, visually confirm complete balloon deflation by fluoroscopy to avoid guiding catheter movement into the vessel and subsequent arterial damage. Carefully read all instructions prior to use. Observe all warnings and precautions noted throughout these instructions. Failure to do so may result in Endovascular treatment of TransAtlantic Inter-Society Consensus II (TASC) D aortoiliac occlusive lesions remains a challenge, but a valuable treatment option in poor surgical candidates. We present our operative technique and midterm results in treating TASC D aortoiliac occlusive disease using unibody bifurcated endografts.

This is not recommended as the proximal end of the stent may catch the edge of the introducer sheath, thus dislodging the stent. The instructions for use provided with the catheter system also recommends not to attempt to pull the device back through the introducer sheath, but to pull the stent and sheath together out of the pt as a unit. The 12/07/2017 · Stent-grafts possess unique advantages over bare metal stents, including plaque exclusion and prevention of in-stent neointimal hyperplasia, improved blood hemodynamics via a new flow lumen, and decreased risk of complications resulting from distal embolization, perforation, rupture, or dissection. 1,9,14,16 The Society for Vascular Surgery

Atrium Physician Education Welcome to Atrium Medical

Icast stent instructions for use

Atrium 85452 Atrium iCast Covered Stent 6mm x 16mm x. Instructions For Use Finder; Zilver® PTX® Drug-Eluting Peripheral Stent Specifications Videos Documents Images. Handle of the Zilver PTX delivery system Zilver PTX Drug-Eluting Peripheral Stent. Indicated for improving luminal diameter for the treatment of de novo or restenotic symptomatic lesions in native vascular disease of the above-the-knee femoropopliteal arteries having reference, Widely used Iliac stent, well-known for its outstanding com-pression resistance. Its Tandem Architecture has been designed to provide excellent conformability to vessel anatomies. The outstanding compression resistance of the EXPRESS Vascular LD Stent makes it an excellent choice for bifurcations or resistant lesions when strength is critical. The Express Vascular LD Iliac Pre-mounted Stent.

Cope Nephroureterostomy Stent Cook Medical. Fenestrated stent graft system. device descriPtioN The Zenith Fenestrated stent graft has been approved to treat patients with short-necked abdominal aortic aneurysms that are ≥ 4 mm in length and those who do not meet the proposed anatomical criteria for the use of infrarenal stent grafts. The device consists of a …, • Prior to implantation of the MERIT ENDOTEK AEROmini Tracheobronchial Stent System, the physician should refer to the Sizing Table (Table 1 & 2) and read the Instructions for Use. • When used in the treatment of stenotic or obstructive lesions, placement of the stent should immediately follow the opening of the airway by.

Outcomes After Stent Implantation for the Treatment of

Icast stent instructions for use

Safety Information AFX - Endologix. This is not recommended as the proximal end of the stent may catch the edge of the introducer sheath, thus dislodging the stent. The instructions for use provided with the catheter system also recommends not to attempt to pull the device back through the introducer sheath, but to pull the stent and sheath together out of the pt as a unit. The https://en.m.wikipedia.org/wiki/Talk:Gunther_Stent 29/03/2009 · Table 3 is a list of commercially available covered stents (used for peripheral indications) in the U.S. Aortic Endografts. The advances in the development of intravascular stents made possible the construction and approval of the currently available endovascular grafts for the treatment of abdominal and thoracic aortic pathology..

Icast stent instructions for use


2017 Endovascular Reimbursement Coding Fact Sheet 1 of 11 The information contained in this document is provided for informational purposes only and represents no statement, promise, • Prior to implantation of the MERIT ENDOTEK AEROmini Tracheobronchial Stent System, the physician should refer to the Sizing Table (Table 1 & 2) and read the Instructions for Use. • When used in the treatment of stenotic or obstructive lesions, placement of the stent should immediately follow the opening of the airway by

29/03/2016 · Stents available for use in the aortoiliac arteries can be divided into balloon-expandable stents, self-expanding stents, and covered stents. Although significant data exist for each stent type, most clinical studies have included patients with relatively less-complex disease. In addition, little comparative data exist between stent types. The stent is indicated for use in occlusions, lesions at high risk for abrupt closure or threatened closure following percutaneous transluminal angioplasty (PTA) or lesions believed to be at high risk of restenosis following PTA in the common iliac, external iliac, or subclavian arteries. The stent is also intended as a palliative treatment of

Atrium Physician Education. Welcome to Atrium's online center for advanced physician training. Atrium has partnered with several thought leaders in the fields of interventional cardiology, endovascular surgery and open surgery to provide physicians with a broad range of training topics. The stent's patented design balances strength and flexibility for proven patency as found in the VISIBILITY ILIAC study. Radiopaque markers on the stent ensure precise placement. Deliver over an 0.035" guidewire for use in the common or external iliac arteries or in the biliary system.

• Prior to implantation of the MERIT ENDOTEK AEROmini Tracheobronchial Stent System, the physician should refer to the Sizing Table (Table 1 & 2) and read the Instructions for Use. • When used in the treatment of stenotic or obstructive lesions, placement of the stent should immediately follow the opening of the airway by The Medtronic Resolute Integrity drug-eluting stent (DES) is among the top three stents on the U.S. market. Outcomes for these stents are very similar, so the stents have largely become a commodity product purchased on price rather than clinical data.

Summary. Prospective, multicenter, non-randomized, single-arm registry to evaluate the safety and effectiveness of the iCAST Covered Stent System in the treatment of patients with symptomatic claudication or rest pain and angiographic confirmation of de novo or restenotic lesions in the common and/or external iliac artery. Summary. Prospective, multicenter, non-randomized, single-arm registry to evaluate the safety and effectiveness of the iCAST Covered Stent System in the treatment of patients with symptomatic claudication or rest pain and angiographic confirmation of de novo or restenotic lesions in the common and/or external iliac artery.

that Cordis offers products for every use or procedure discussed and the FDA-cleared or approved labeling for all products may not be consistent with the information in this guide. As always, please refer to the product’s instructions for use or package insert for a complete description of indications and contraindications for any medical The stent is indicated for use in occlusions, lesions at high risk for abrupt closure or threatened closure following percutaneous transluminal angioplasty (PTA) or lesions believed to be at high risk of restenosis following PTA in the common iliac, external iliac, or subclavian arteries. The stent is also intended as a palliative treatment of

Specific follow-up guidelines are described in the Instructions For Use under, Imaging Guidelines and Post-Operative Follow-up. After endovascular graft placement, patients should be regularly monitored for perigraft flow, aneurysm growth or changes in the structure or position of the endovascular graft. Use of a PTFE-covered BE stent (iCast Covered Stent, Atrium Medical Corp, Hudson, NH; or Graft Master Stent, Abbott Vascular Devices, Santa Clara, CA) is another potential method to treat renal ISR, although neither device is approved for this indication, nor is there evidence to support their use.

The iCAST covered stent provides deployment accuracy due to its precision stent delivery platform and its low foreshortening design. The iCAST stent is crafted using Atrium’s PTFE encapsulation technology and a one-step deployment technique for precise, accurate deployment. Proven across a broad range of complex cases, the versatility of the GORE® VIABAHN® Endoprosthesis with Heparin Bioactive Surface* enables you to deliver high patency and durable outcomes to minimize interventions for your patients.

These explanted stents showed no evidence of in-stent growth at a follow-up of 3 weeks. 15 Gordon and Moore 9 subsequently showed the effective use of iCAST stents in 3 patients with refractory PVS with patency at 6 months after implantation. Though these studies and our observations of the iCAST stent show promise for application in PVS atrium iCAST™ Balloon expandable Covered Stent. Atrium’s iCAST™ balloon expandable covered stent is FDA 510(k) cleared for the treatment of tracheobronchial strictures. The iCAST covered stent provides deployment accuracy due to its precision stent delivery platform and its low foreshortening design. The iCAST stent is crafted using Atrium’s PTFE encapsulation technology and a one-step deployment …