MicroAire must now apply for the Endotine CE Mark under the forthcoming EU Medical Device Regulation (MDR). The new regulation is much more complicated than the MDD and there is already a lengthy queue for approvals at BSI. Therefore, Endotine will continue to be unavailable for a long time, perhaps throughout all of 2020 and into 2021.
Read MoreEndotine devices are still awaiting their CE mark from BSI. MicroAire have submitted the required clinical data and are waiting on a response.
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