www.fdanews.com/articles/75941-curatronic-s-biomove-3000-gets-ce-mark
CURATRONIC'S BIOMOVE 3000 GETS CE MARK
August 31, 2005
Israel-based Curatronic has obtained CE certification for the Biomove 3000 Stroke Rehabilitation system for marketing in the EU.
The Biomove 3000 system was specifically developed for home therapy following a stroke. The battery-powered device detects extremely small electrical EMG signals that persist in paralyzed muscles after a stroke and uses these tiny signals to initiate an electrical stimulation impulse to the muscles, resulting in actual muscle movement by the patient.
The CE marking follows FDA approval of the device earlier this year.