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and is a CE Marked device cleared for sale in the European Union, Switzerland, Australia and Israel. Approved Indication The FDA has approved the NovoTTF-100A System for use as a treatment for

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GlucoTrack® Model DF-F obtained a CE Mark approval in Europe and final CE Mark approval in March 2014 and recently received approval to market the device also to pre-diabetics.

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PR Newswire: press release distribution, targeting, monitoring and marketing - GlucoTrack® Moves Forward with FDA Approval Process

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