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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.

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