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Aortic Balloon Articles & Analysis

7 news found

Anteris reports successful interim results for the first-in-human trial for DurAVR

Anteris reports successful interim results for the first-in-human trial for DurAVR

“The excellent results observed so far are a function of the proprietary 3D single-piece leaflet design of DurAVR™ that mimics a native aortic valve. These numbers are even more remarkable considering this cohort had small annular anatomy. ...

ByAnteris Technologies Limited


Neurescue`s Breakthrough Intelligent Balloon Catheter FDA 510(k) Cleared for Hemorrhage Control and IDE Approved for Cardiac Arrest

Neurescue`s Breakthrough Intelligent Balloon Catheter FDA 510(k) Cleared for Hemorrhage Control and IDE Approved for Cardiac Arrest

The NEURESCUE device is the world’s first intelligent balloon catheter for aortic occlusion, an emergency technique that supercharges blood flow to the heart and brain within one minute from deployment. The catheter-based device is delivered via the femoral artery, temporarily inflating a soft balloon in the aorta to redirect blood flow ...

ByNeurescue


Neurescue Announces Appointment of Medtronic Veteran Mette-Marie Harild to Company’s Board of Directors

Neurescue Announces Appointment of Medtronic Veteran Mette-Marie Harild to Company’s Board of Directors

COPENHAGEN, Denmark--(BUSINESS WIRE)--Neurescue, a clinical-stage medical device company bringing to market the world’s first computer-aided balloon catheter for aortic occlusion, today announced that medical device industry veteran Mette-Marie Harild has been appointed to the Neurescue board of directors. ...

ByNeurescue


Carmat outlines commercial and development plan for its total artificial heart

Carmat outlines commercial and development plan for its total artificial heart

[6] GlobalData: EU5 Cardiac Assist Devices Market Outlook To 2025 – Intra-Aortic Balloon Pumps, Mechanical Circulatory Support Devices And Short-Term Circulatory Support Devices (Report GDMECR1561DB) [7] The initial inclusion target for this study was 20 patients, a figure that can be adjusted up or down during the course of the study. ...

ByCarmat


Colibri Heart Valve to Present Patient Follow-up Results from Clinical Feasibility Study of Second-Generation TAVI System at TCT

Colibri Heart Valve to Present Patient Follow-up Results from Clinical Feasibility Study of Second-Generation TAVI System at TCT

Fish stated, “The post-implantation measures of aortic valve pressure gradients and paravalvular leakage continue to be favorable at six months following implantation. ...

ByColibri Heart Valve LLC


Colibri Heart Valve Continues Enrollment in Clinical Feasibility Study of Second-Generation TAVI System

Colibri Heart Valve Continues Enrollment in Clinical Feasibility Study of Second-Generation TAVI System

Initial post-implantation results from these patients, who received a 24mm valve, show favorable low aortic valve pressure gradients and no observed paravalvular leakage or aortic insufficiency. ...

ByColibri Heart Valve LLC


Colibri Heart Valve Advances Second-Generation TAVI System into Clinical Feasibility Study

Colibri Heart Valve Advances Second-Generation TAVI System into Clinical Feasibility Study

Colibri Heart Valve LLC, a privately held emerging medical device company, today announced that the first two patients have been successfully enrolled in a clinical early feasibility study (EFS) of the company’s disruptive second-generation ready-for-use balloon-expandable transcatheter aortic valve implantation (TAVI) system. As with Colibri’s ...

ByColibri Heart Valve LLC

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