Country for PR: United Kingdom
Contributor: PR Newswire Europe
Friday, September 06 2019 - 21:08
AsiaNet
Occlutech AFR Heart Failure Device Obtains CE Mark Approval
SCHAFFHAUSEN, Switzerland, Sept. 6, 2019 /PRNewswire-AsiaNet / --

Occlutech AG announced today that its atrial flow regulator, the Occlutech AFR 
device, has obtained CE mark approval clearing it for sales on the European CE 
regulated market. Occlutech AFR is a next generation intra-atrial shunt device, 
intended to treat heart failure symptoms by decompressing abnormal intra-atrial 
pressure. It is placed in the septum between the left atrium and right atrium 
in a minimally invasive procedure. It is manufactured in different sizes 
thereby allowing unique patient-oriented and individualized treatment.  

(Logo - 
https://mma.prnewswire.com/media/971275/Occlutech_International_AB_Logo.jpg ) 

In Europe and around the world, millions of patients suffer from heart failure 
and several hundred thousand die from this condition every year. Many of these 
patients suffer from decreasing cardiac output that originates from a 
malfunction of the left heart. As a consequence, the left atrium will dilate 
and become volume and pressure overloaded.  This leads to the most important 
clinical symptom of heart failure, i.e. pulmonary congestion and shortness of 
breath. By placing the Occlutech AFR device into the septum and creating a 
restrictive atrial septal opening by maintaining the correct sizing of a 
created shunt, the intra cardiac pressure is substantially reduced, thereby 
improving the heart's function.

"With CE mark approval of the Occlutech AFR we are taking another big step 
towards becoming a multi-franchise congenital and structural heart disease 
therapy provider." says Sabine Bois, Co-CEO of Occlutech AG. Additionally, she 
states that "the Occlutech AFR with its efficacy, versatility, convenience and 
safety has true potential to revolutionize the way heart failure patients are 
treated."

Occlutech is one of the leading companies in its field, with several major 
products including state-of-the-art PFO occluders, ASD occluders among others. 
Occlutech has sales of congenital and structural heart products in over 80 
countries and maintains manufacturing and R&D facilities in Jena, Germany and 
Istanbul, Turkey. Occlutech has developed many novel products and technologies 
to improve treatment of patients in these and related areas. (www.occlutech.com)

Contact:

Sabine Bois
Co-CEO Occlutech Group
Mobile: +49-160-90792130
Email: sabine.bois@occlutech.com

Susanne Göransson
Executive Assistant
Mobile: +46-704-33-65-21
Email: susanne.goransson@occlutech.com 

 
Source: Occlutech International AB    
Translations

Japanese