This month sees us complete transfer of our CE certification to Kiwa, our new Notified Body, following notification from LRQA of withdrawal of services relating to the Medical Device Directive (MDD) last year.

This follows over six months of work on the part of our Regulatory team, supported by the Quality and Product Management teams; and will ensure that we can continue to provide our life-saving medical devices to hospitals around the world.

Our next goal is to transfer over to the new Medical Device Regulation (MDR) over the next 3 years.