Re-classification of LGF now complete and looking to the future

Endovab is very happy to announce that the medical device re-classification process now is completed: The Liungman Guidewire Fixator CE mark Class 3 (MDD) is valid until May 2024.

We look forward to continuing to supply this key tool to all endovascular centres in Europe, which will help them make interventions in the aorta and the peripheral artery safer and in a shorter time.

2017 > 10

A technical paper describing a new method for f-EVAR has just been published in INNOVATION. The new method entails fixated guidewires and retrograde lining of the aortic branches, which eliminates the unpredictable searching of the branched vessels during fenestrated endovascular aortic repair. 
"This publication is an important step in spreading the knowledge and awareness of a new method to solve a well know challenge in fenestrated and branched aortic repair.” says Krister Liungman, Inventor of the Guidewire Fixator. 

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2017 > 10

A technical paper describing a new method for f-EVAR has just been published in INNOVATION. The new method entails fixated guidewires and retrograde lining of the aortic branches, which eliminates the unpredictable searching of the branched vessels during fenestrated endovascular aortic repair. 
"This publication is an important step in spreading the knowledge and awareness of a new method to solve a well know challenge in fenestrated and branched aortic repair.” says Krister Liungman, Inventor of the Guidewire Fixator. 

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