The BST Device Features and Specifications

The BST Device - Features

  • The BST Device intended use is approved for hospitals, clinics and home care in Europe, Canada, Brazil and Israel (FDA approval is on process).
  • The BST Device is comprised of two basic elements: a computerized controlled single channel bioelectrical stimulator and a pair of E-QURE's surface electrodes.
  • The BST Device transmits a low intensity bio-current (micro-current density 0.3mA r.m.s./cm2). 
  • The BST Device treatment is operated through the E-QURE's surface electrodes attached to the skin.  The surface electrodes are placed on the healthy skin near the wound. The electrodes skin interface has a hypoallergenic conductive layer, which enables the use of a single pair of electrodes for 1 to 3 days.
  • The BST Device treatment is used three times a day, for 30 minutes each (according to the physician's recommendations). Only during these treatment sessions the patient is connected to the device, enabling full flexibility and movement during the rest of the day.

Warning: use of electrodes not according to their labelled usage time may results in skin adverse effects, reduced efficacy and patient compliance.

BST - Specifications

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E-QURE Corp.

20 West 64th street - Suite 39G
New York, NY 10023

Office: +972-8-9167333
Fax: +972-8-9167331

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