Tag: bd
Vascular News’ top 10 most popular stories of March 2024
Transcarotid artery revascularisation (TCAR) features in three of March's most popular Vascular News stories, with a talk on the future of aortic repair and...
Rotarex™S: A 25-year legacy continues
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This year marks a significant milestone as BD celebrates 25 years...
BD announces first patient enrolled in PAD vascular covered stent trial
BD has announced the enrolment of the first patient in the AGILITY investigational device exemption (IDE) study, which will assess the safety and effectiveness...
Promising future previewed for PAD treatment at Riga summit
This advertorial is sponsored by BD.
There has been major progress in the treatment of peripheral arterial disease (PAD) globally in the last few years,...
Vascular News’ top 10 most popular stories of August 2022
The establishment of the first-ever global consensus for the appropriate use of intravascular ultrasound (IVUS) in lower extremity and arterial and venous interventions, results...
BD launches first-in-human trial of a peripheral sirolimus drug-coated balloon
BD has announced the start of enrolment in a first-in-human trial of a peripheral sirolimus drug-coated balloon (DCB).
The PREVISION trial is a prospective, multicentre,...
Vascular News’ top 10 most popular stories of July 2022
July's top 10 most popular items include more from this year's Society for Vascular Surgery (SVS) Vascular Annual Meeting (VAM 2022; 15–18 June, Boston,...
AVeVA study confirms benefit of covered stent placement in graft-vein anastomotic...
A prospective, multicentre study involving the Covera vascular covered stent (BD) has confirmed the benefits of immediate, post-percutaneous transluminal angioplasty (PTA) placement of the...
New data support covered stent use in complex aortoiliac occlusive disease...
One-year outcomes from the BELSTREAM trial add to a growing pool of data that covered stents are safe and effective in the treatment of...
Vascular access creation: EndoAVF keeps future options open, but is not...
Based on over four years of experience in a single centre, Robert Shahverdyan (Asklepios Klinik Barmbek, Hamburg, Germany) claims that endovascular arteriovenous fistula (endoAVF)...
Case report: Aspirex™S enables treatment of thrombosed prosthetic arteriovenous grafts
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“Percutaneous mechanical thrombectomy debulks thrombus load, leading to rapid revascularisation for...
BD launches new Crosser iQ CTO recanalisation system
BD has announced the launch and US Food and Drug Administration (FDA) 510(k) clearance for the Crosser iQ chronic total occlusion (CTO) recanalisation system,...
Vascular News’ top 10 most popular stories of October 2021
New data from a head-to-head, randomised trial comparing vascular closure devices, highlights from CX Aortic Vienna 2021 (5–7 October, broadcast) and an interview with past Society...
BD announces 510(k) clearance of expanded indications for the Rotarex atherectomy...
BD recently announced it has received 510(k) clearance for expanded indications from the US Food and Drug Administration (FDA) for the Rotarex atherectomy system.
The...
The WavelinQ™ EndoAVF System takes an innovative approach in creating endovascular...
NOTE: This advertorial is ONLY available to watch in selected countries and geographies
This advertorial, sponsored by BD, is intended for readers in the...
Why Rotarex is my first choice treatment in patients with bypass...
NOTE: This video is ONLY available to watch in selected countries and geographies
Bruno Migliara (Peschiera del Garda, Italy) talks to Vascular News about the reasons...
Case report: Recanalisation of chronic iliofemoral venous occlusion in a patient...
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In this case report for Vascular News, experts outline the importance...
Case report: Recanalisation of a long SFA occlusion with Ultrascore™ Focused...
This advertorial, sponsored by BD, is only available in selected countries and geographies.
“Improving vessel compliance with focused force longitudinal plaque fracture seems to...
BD announces enrolment in postmarket studies of the WavelinQ endoAVF system
BD announced today that enrolment has begun and the first patients have been treated in the postmarket surveillance study, CONNECT-AV.
CONNECT-AV is a prospective, single-arm,...
Case report: Complex endovascular treatment for an iliac artery occlusion using...
This advertorial, sponsored by BD, is only available in selected countries and geographies.
Martin Schroeder—a vascular surgery specialist at the Ruhr University Bochum Marienhospital...
FDA advisory panel recommends against premarket approval of Lutonix 014 DCB...
A US Food and Drug Administration (FDA) advisory panel has recommended against premarket approval of BD’s Lutonix 014 drug-coated balloon (DCB) for use in...
Six-month results of Lutonix AV Global registry published
Six-month results of the Lutonix arteriovenous (AV) Global registry were recently published in the Journal of Vascular and Interventional Radiology (JVIR). The data confirm...
CLEAN3 trial outlines potential new best practices for peripheral IV catheters
BD today announced that new clinical data have found robust evidence that using a vascular care solution can help improve outcomes for patients requiring...
Ellipsys system offers greater patient eligibility and reduced time to dialysis,...
Two devices for creating minimally invasive dialysis access—the Ellipsys vascular access system (Avenu Medical) and the WavelinQ 4F system (BD)—demonstrated high rates of technical...
24-month AVeNEW study results: Covered stent angioplasty “statistically superior” to angioplasty...
Against the backdrop of increasing end-stage renal disease (ESRD) prevalence in the USA, Bart Dolmatch (Portola Valley, USA) presented the 24-month results of the...
BD announces launch of Halo One thin-walled guiding sheath
BD has announced the launch of the Halo One thin-walled guiding sheath, designed to perform as both a guiding sheath and an introducer sheath,...
Straub Medical acquired by BD
Straub Medical has approved a full acquisition by Becton, Dickinson and Company (BD). The acquisition was completed on 20 April 2020. Straub Medical manufactures,...
A Deeper Dive into the Venovo™ Venous Stent System
The venous space continues to evolve in the United States, and many physicians are learning how to navigate through the challenges of the venous...
A Deeper Dive into the Venovo™ Venous Stent System
Vascular News talks with Gerard O'Sullivan, FSIR, FEBIR, University College Hospital, Galway, Ireland. This article is supported by BD Interventional.
Disclosures: Dr. Gerard O'Sullivan reports...
LINC 2020: BD announces long-term safety data for BTK drug-coated balloon
Today at the 2020 Leipzig Interventional Course (LINC; 28–31 January, Leipzig, Germany), BD announced that interim findings from the Lutonix below-the-knee (BTK) investigational...
BD announces publication of drug-coated balloon safety data for femoropopliteal PAD
BD has announced the publication of a company-initiated, independent analysis of the Lutonix 035 drug-coated balloon (DCB) femoropopliteal clinical programme in the Journal of...
FDA notifies BD that Lutonix paclitaxel balloon PMA application for below...
The US Food and Drug Administration (FDA) have denied BD premarket approval (PMA) for the company’s Lutonix drug-coated balloon (DCB) in the treatment of...
FDA notifies BD that Lutonix paclitaxel balloon PMA request for below...
The US Food and Drug Administration (FDA) have denied BD premarket approval (PMA) for the company’s Lutonix drug-coated balloon (DCB) in the treatment of...
BD receives FDA approval for expansion to drug-coated balloon product line
The US Food and Drug Administration (FDA) has approved expanded sizes of the Lutonix 018 drug-coated balloon (DCB) to treat long superficial femoral artery...
BD announces launch of UltraScore 014 Focused Force PTA Balloon
BD has announced the launch of their UltraScore 014 Focused Force percutaneous transluminal angioplasty (PTA) Balloon. This marks the first scoring balloon with sheath...
BD receives FDA 510(k) clearance of WavelinQ 4F endoAVF system
BD has announced the 510(k) clearance from the US Food and Drug Administration (FDA) for the WavelinQ 4F endoAVF system earlier this month. The endoAVF...
Lutonix BTK randomised trial meets safety and efficacy endpoints at six...
Six-month outcomes of a multicentre randomised controlled trial using the Lutonix 014 drug-coated balloon (BD; DCB) has demonstrated the DCB is safe to use...
BD acquires TVA Medical, makers of everlinQ endoAVF System
BD (Becton, Dickinson and Company) announced it has completed the acquisition of TVA Medical, a company that develops minimally invasive vascular access solutions...
BD announces completion of enrolment in Lutonix 014 DCB below-the-knee trial
Enrolment is complete in the Lutonix below-the-knee trial with BD planning to submit a pre-market approval application to the US Food and Drug Administration...
BD completes acquisition of Bard
BD, a leading global medical technology company, has announced it has completed the acquisition of C R Bard, creating a new health care industry...
European Commission approves BD acquisition of Bard, subject to conditions
The European Commission has approved, under the EU Merger Regulation, the acquisition of Bard by BD. The decision is conditional on the divestment of...
BD to acquire Bard for US$24 billion
BD (Becton, Dickinson and company) has definitively agreed to acquire Bard for US$317 per common share in cash and stock, for a total consideration...
