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EUROPE. Company Directory


Bentley InnoMed GmbH

Lotzenäcker 3 , 72379 Hechingen, Germany

PHONE: +49 (0) 7471 984 995 10

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Catheters / Specialty Catheters

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Company Name Product Name Catheter Size (F) Working Length (cm) Minimum Guiding Catheter ID (inch) Comments
Bentley InnoMed GmbH BeBack crossing catheter 2.9, 4 80, 120 2.9 F (crossover 5 F); 4 F (crossover 6 F) A low-profile support catheter that has a crossing and targeted re-entry capability due to the steerable nitinol needle at the tip; a radiopaque marker indicates the direction in which the curved needle will protrude from the catheter’s tip; antegrade, retrograde, and crossover are possible for intraluminal and subintimal approach on 0.014- and 0.018-inch wire platform

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Stents / Balloon-Expandable Covered Stents

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Company Name Product Name Material Used Maximum Guidewire Size (inch) Introducer Size (F) Stent Diameter (mm) Stent Length (mm) Delivery System Length (cm) CE Mark Indications
Bentley InnoMed GmbH BeGraft Cobalt chromium (L605), ePTFE 0.035 6 (diameter: 5–8 mm), 7 (diameter: 9–10 mm) 5, 6, 7, 8, 9, 10 18, ~23, ~28, ~38, ~58 75, 120 Intraluminal chronic placement in iliac and renal arteries for restoring and improving the patency and to treat aneurysms, acute perforations, ruptures and fistulas
Bentley InnoMed GmbH BeGraft aortic Cobalt chromium (L605), ePTFE 0.035 9 (diameter: 12 mm); 11 (diameter: 14, 16 mm); 14 (diameter: 18–24 mm) 12, 14, 16, 18, 20, 22, 24 19, 29, ~38, ~48, ~58 75, 120 Implantation in the native and/or recurrent coarctation of the aorta on adolescent or adult patients; restores and improves the patency of the iliac arteries
Bentley InnoMed GmbH BeGraft coronary Cobalt chromium (L605); ePTFE 0.014 5 (guide catheter) 2.5, 2.75, 3, 3.5, 4, 4.5, 5 8, 12, 16, 18, 21, 24 144, 154 Transluminal implantation in coronary arteries or aortocoronary bypass grafts for the treatment of (1) acute perforation or rupture of coronary arteries; and (2) aneurysm of coronary arteries or coronary bypass-vein graft
Bentley InnoMed GmbH BeGraft peripheral Plus Double cobalt chromium (L605), double ePTFE (in sandwich design) 0.035 7 (diameter: 5–8 mm); 8 (diameter: 9–10 mm) 5, 6, 7, 8, 9, 10 ~27, ~37, ~57 120 Intraluminal chronic placement in iliac and renal arteries for restoring and improving the patency and to treat aneurysms, acute perforations, ruptures, and fistulas
Bentley InnoMed GmbH BeFlared FEVAR CoCr (L-605), ePTFE covering folded inside and clamped on both ends 0.035 6, 7 5/8, 6/8, 7/10, 8/10, 9/11 22–37 120 Indicated for use as a bridging stent graft in patients requiring endovascular abdominal aortic aneurysm repair with a fenestrated aortic endovascular graft to keep the visceral artieries perfused
Bentley InnoMed GmbH BeFlow iliac CoCr (L-605)m ePTFE covering folded inside and clamped on both ends 0.035 6, 7 7, 8, 9, 10 37, 57 75 Permanent intraluminal placement in iliac arteries for restoring and improving the patency impaired by arteriosclerosis or other stenoses that may be treated by stenting
Bentley InnoMed GmbH BeGraft Plus CoCr (L-605) 0.035 7/8 F 5 for Ø 5 - 7 mm (depending on indication and access site) 8 F for Ø 8 mm 8/9/10 F 5 for Ø 9 and 10 mm (depending on indication and access site) Ø 5 and 6 mm (SV = small vessel design) Ø 7 and 8 mm (MV = medium vessel design) Ø 9 and 10 mm (LV = large vessel design) 28, 38, 58, 78 (SV = small vessel design) 27, 37, 57, 77 (MV = medium vessel design, LV = large vessel design) 120 Indicated for permanent intraluminal placement in iliac and renal arteries for restoring and improving the patency impaired by arteriosclerosis or other stenoses that may be treated by stenting; sealing aneurysms, acute perforations, acute ruptures, and fistulas; as bridging stent graft in patients requiring endovascular abdominal aortic aneurysm repair with a branched aortic endovascular graft to keep the visceral arteries perfused Sizes approved when used for permanent intraluminal placement in iliac and renal arteries: Ø 5 mm and 6 mm in lengths of 28 mm, 38 mm, and 58 mm, Ø 7 mm - 10 mm in lengths of 27 mm, 37 mm, and 57 mm Sizes approved when used as a bridging stent graft for BEVAR: Ø 5 mm and 6 mm in lengths of 38 mm, 58 mm, and 78 mm, Ø 7 mm - 10 mm in lengths of 37 mm, 57 mm and 77 mm

Stents / Balloon-Expandable Stents

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Company Name Product Name Material Used Maximum Guidewire Size (inch) Introducer Size (F) Stent Diameter (mm) Stent Length (mm) Delivery System Length (cm) CE Mark Indications
Bentley InnoMed GmbH BeSmooth peripheral Cobalt chromium (L605) 0.035 6 5, 6, 7, 8, 9, 10 18, 23, ~27, 38, ~57 75, 120 Treatment of de novo or restenotic atherosclerotic lesions in protected peripheral arteries

Stents / Venous Stents

View Chart
Company Name Product Name Stent Material Cell Design Introducer Size (F) Guidewire Compatibility (inch) Stent Diameter (mm) Stent Length (mm) Delivery System Delivery System Length (cm)
Bentley InnoMed GmbH BeYond venous Nickel-titanium alloy (nitinol) Open cell design; closed cell stent ends 10 0.035 10–18 60–150 Pull-back technique; radiopaque marker on catheter tip 100

Other Devices / CTO Crossing Devices

View Chart
Company Name Product Name Catheter Size (F) Wire Size (inch) Working Length (cm) Minimum Guiding Catheter ID (inch) Comments
Bentley InnoMed GmbH BeBack crossing catheter 2.9, 4 0.014, 0.018 80, 120 2.9 (crossover 4), 4 (crossover 6) A low-profile support catheter that has a crossing and targeted re-entry capability due to the steerable nitinol needle at the tip; a radiopaque marker indicates the direction in which the curved needle will protrude from the catheter’s tip; antegrade, retrograde, and crossover are possible for intraluminal and subintimal approach on 0.014- and 0.018-inch wire platform

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Aortic (AAA) Aortic (TAA) Balloons Catheters Embolization Sheaths Stents Wires Other Devices View All

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Carotid Coding Dialysis Embolization EVAR HTN Limb Salvage Neurointervention Oncology Radial Regulatory Renal SFA TEVAR Venous
Centers

Carotid Coding Dialysis Embolization EVAR HTN Limb Salvage Neurointervention Oncology Radial Regulatory Renal SFA TEVAR Venous

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