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bioPlux clinical

bioPlux clinical is oriented for clinical biofeedback applications. The system includes 4 sEMG active sensors that allow monitoring of up to 4 muscles.
The Biofeedback Software Package allows the clinician to manage, monitor, and record multiple dynamic protocols and sessions for different patients.
Additional sensors can be used to expand the device functionalities.
The bioPLUX clinical is in compliance with essential requirements established by the Annex I of the Directive 93/42/CEE, of July 14, and decree law 30/2003, of February 14, not being the device a risk to the health and safety of the patients, users or other agents, since it be used according to the aim that was conceived.
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