(Bild: Redaktion Devicemed; KI-generiertes Symbolbild) Die FDA hat die Zweckbestimmung des ballonexpandierbaren ...
FEVAR and BEVAR transformed how complex aortic aneurysms are treated. Clinicians now have an FDA-approved bridging stent option specifically indicated for these procedures.
The expanded indication covers the device’s use as a bridging stent in fenestrated and branched aortic repair.
The balloon-expandable device can now be used as a bridge in fenestrated and branched endovascular aortic repair.
Gore & Associates announced FDA approval of an expanded indication for the company’s Viabahn VBX balloon expandable e ...
W. L. Gore & Associates' medical business (Gore) today announced U.S. Food and Drug Administration approval of an expanded indication for the GORE® VIABAHN® VBX Balloon Expandable Endoprosthesis (VBX ...
Gore today announced US Food and Drug Administration (FDA) approval of an expanded indication for the company's Viabahn VBX ...
Home Operatie bij een aneurysma van de buikslagader via de liezen (EVAR) Bij deze operatie plaatst de vaatchirurg via kleine sneetjes in de liezen een kunststof vaatprothese (stent) in de buikslagader ...
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