Due to Brexit, the United Kingdom is updating its medical device regulations and introducing a new route (UKCA marking) to place medical devices on the UK market. The new legislative framework had been expected to come into force on July 1st, 2023.
Due to a delay in the establishment of the new regulations, the deadline has been extended to July 1st, 2024. This means CE marked medical devices can continue to be placed on the UK market until June 2024.
This means that, since Fluidda’s Broncholab® application already has a CE mark, it is available for use in the UK market at least until June 2024.
For more information on Broncholab, please visit www.broncholab.com
Categorised in: Miscellaneous / November 3, 2022 9:38 am /Tags: Broncholab, CE