BEUDAMED
    14 results · 31ms · Sources: EU EUDAMED, US FDA

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    Brand Name: AFX" Introducer System, Model Number S17-45. Lot Numbers: 1079840, 1079843, 1079844, 1079845. Product Usage: The AFX Introducer System is intended for use to facilitate the introduction of catheters and other medical devices into the vasculature and to minimize blood loss associated with such introduction.

    FDA Recall
    Terminated ·Endologix Inc·Product code DYB·May 13, 2013

    Powerlink System with IntuiTrak Delivery System (Endovascular Graft): Model Number 34-34-80L, LOTS W09-2966 AND W09-2998.

    FDA Recall
    Terminated ·Endologix Inc·Product code OAD·November 25, 2009

    Powerlink System for Abdominal Aortic Aneurysm (Endoluminal Bifurcated Prosthesis with Delivery System) Model No. 25-16-155BL

    FDA Recall
    Terminated ·Endologix Inc·Product code MIH·December 14, 2005

    Powerlink System for Abdominal Aortic Aneurysm (Endoluminal Bifurcated Prosthesis with Delivery System) Model No. 25-16-155BL

    FDA Recall
    Terminated ·Endologix Inc·Product code MIH·December 14, 2005

    Powerlink System for Abdominal Aortic Aneurysm (Endoluminal Bifurcated Prosthesis with Delivery System) Model No. 25-16-140BL

    FDA Recall
    Terminated ·Endologix Inc·Product code MIH·December 14, 2005

    Powerlink System for Abdominal Aortic Aneurysm (Endoluminal Bifurcated Prosthesis with Delivery System) Model No. 25-16-135BL

    FDA Recall
    Terminated ·Endologix Inc·Product code MIH·December 14, 2005

    Powerlink System for Abdominal Aortic Aneurysm (Endoluminal Bifurcated Prosthesis with Delivery System) Model No. 28-16-140BL

    FDA Recall
    Terminated ·Endologix Inc·Product code MIH·December 14, 2005

    Ovation iX Abdominal Stent Graft Systems, REF: TV-AB2080-I, TV-AB2080-J, TV-AB2380-I, TV-AB2380-J, TV-AB2680-I, TV-AB2680-J, TV-AB2980-I, TV-AB2980-J, TV-AB3480-I, TV-AB3480-J

    FDA Recall
    Terminated ·Endologix, Inc.·Product code MIH·May 6, 2020

    Endologix Infrarenal Bifurcated Powerlink System with Visifiex Delivery System (endovascular graft). Model Number 25-16-155BL

    FDA Recall
    Terminated ·Endologix Inc·Product code MIH·November 8, 2006

    Powerlink System for Abdominal Aortic Aneurysm (Endoluminal Bifurcated Prosthesis with Delivery System) Model No. 28-16-155BL

    FDA Recall
    Terminated ·Endologix Inc·Product code MIH·December 14, 2005

    Powerlink System for Abdominal Aortic Aneurysm (Endoluminal Bifurcated Prosthesis with Delivery System) Model No. 28-16-135BL

    FDA Recall
    Terminated ·Endologix Inc·Product code MIH·December 14, 2005

    Powerlink System for Abdominal Aortic Aneurysm (Endoluminal Bifurcated Prosthesis with Delivery System) Model No. 25-16-140BL

    FDA Recall
    Terminated ·Endologix Inc·Product code MIH·December 14, 2005

    Powerlink System with IntuiTrak Delivery System (Endovascular Graft): Model Number 34-34-80LE, LOTS W09-2967 AND W09-3000.

    FDA Recall
    Terminated ·Endologix Inc·Product code OAD·November 25, 2009

    Endologix Infrarenal Bifurcated Powerlink System with Visifiex Delivery System (endovascular graft), Model Number 28-16-155BL

    FDA Recall
    Terminated ·Endologix Inc·Product code MIH·November 8, 2006