Provizio® SEM Scanner

The world’s first and only FDA authorized handheld device to objectively alert clinicians to specific anatomical areas of a patient’s body at increased risk for developing pressure injury. By providing clinicians information on increased pressure injury risk 5 days (median) earlier than Visual Skin Assessments, the device facilitates earlier and anatomically specific interventions designed to reverse the damaging effects of pressure injuries and prevent pressure injuries from breaking through the skin (Okonkwo et al, 2020).

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