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FDA Approves CardioQ-EDM+

On 23 October 2013, the US Food and Drug Administration (FDA) approved the launch of the CardioQ-EDM+ monitor in the American market place.  The EDM+ has already generated considerable interest amongst leading US Clinicians. With a strong foothold already in the USA via the EDM (first generation monitor), Deltex are confident that combining two previously competing technologies, it offers doctors a wider of range patients’ haemodynamic status resulting in the Companys’ ability to grow the US hospital base and recurring probe related revenue.