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MediValve’s CE clearance for the acWire Guidewire

Manufacturing Group | January 11, 2014

The acWire device is specifically intended for implantation plane acquisition, during Trans-catheter Aortic-Valve Implantation (TAVI) procedures.

MediValve Ltd. officials announced that the company has received European pre-market clearance for the acWire Guidewire[1],[2] following review of a technical file submission by the Institute for Testing and Certification Inc (ITC). The European pre-market clearance completes the Conformité Européenne, or European Conformity (CE) registration process. The acWire is specifically intended for implantation plane acquisition, during Trans-catheter Aortic-Valve Implantation (TAVI) procedures, using fluoroscopic imaging.

Previously, MediValve completed filing a pre-marketing notification application (510(k)) with the U.S. Food and Drug Administration (FDA) for the acWire.

Assaf Klein, CEO for MediValve commented, "We are thrilled to have reached the milestone of receiving CE pre-market clearance of the acWire. We anticipate significant clinical interest for this innovative technology. This is the first in a series of regulatory applications while we continue our development of several additional acWire products."

Gad Keren, MD[3], chairman of the Department of Cardiology, Tel-Aviv University's Sackler School of Medicine, commented, "Accurate positioning of interventional medical devices within the cardiovascular system is critical to patient safety and successful clinical outcomes. The acWire technology now being developed by MediValve holds the promise of addressing both critical needs. With an aging population world-wide and an increasing incidence of cardiovascular interventions, the clinical community will look for solutions that increase patient safety and facilitate uniform and consistent clinical results. I look forward to acWire entering the clinic."

About the MediValve Ltd., acWire Guidewire
The MediValve acWire Guidewire  is a single-use, fully disposable medical device utilizing innovative shape-memory alloy technology intended to enable identification of cardiovascular structures utilizing existing imaging methods.  Use of acWire employs methods and techniques currently utilized by interventional cardiologists to access the cardiovascular system. Once directed to a selected cardiovascular location, acWire is deformable under fluoroscopy to identify a desired specific anatomical landmark for subsequent therapeutic treatment by the clinician. acWire is designed to facilitate the accurate placement and alignment of medical devices in the cardiovascular system during diagnostic and interventional procedures.

MediValve Ltd., was founded in 2010, it is a portfolio company of The Trendlines Group. MediValve is developing the acWire Guidewire to facilitate the accurate placement of medical devices in the cardiovascular system during diagnostic and interventional procedures.

1. This product is not approved for sale in the US.

2. Patents pending.

3. Dr. Keren is a member of the MediValve Board of Directors and the chairman of the Medical Advisory Board

Source: MediValve

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