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Approved medical device Safe and simple to use

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Medical device – A product you can trust in

WiTouch® Pro is a wearable transcutaneous electrical nerve stimulator with Bluetooth® technology for control via a smartphone App, and is a Class IIa Medical Device. The device has met the following National and International regulations and quality standards.

  •   Medical Device Class IIa

      Medical Device Class IIa

    Approval can only be affixed to a Medical Device when it meets the strict requirements of the directive.

  • ISO 13485: 2016

    ISO 13485: 2016

    Only given to medical devices that consistently meet customer requirements and regulatory standards.

  • TÜV SÜD Medical Health Services

    TÜV SÜD Medical Health Services

    Auditor of Hollywog’s Quality Management System ensuring compliance with the latest directives, regulations, and standards.



    International Standards and Conformity Assessment for all electrical, electronic and related technologies