Company News

Regulatory requirement communication

During a recent quality and regulatory review of our product range, we recognised that a number of our component products and QA stretcher accessories should no longer be classified as a medical device in their own right. We have undertaken the work required to de-register them as a medical device, but please be assured that they remain subject to our rigorous quality and regulatory systems and remain available for you to purchase.


For the product affected by this update please refer to this document.

Share this