The MHRA has appointed two new UK Approved Bodies for medical devices, namely the UK affiliates of EU Notified Bodies TÜV Rheinland and TÜV SÜD. The former has also been designated as an Approved Body for in vitro diagnostic medical devices (IVDs). This means there are now six UK Approved Bodies capable of conducting UKCA conformity assessments for general medical devices.
The last organisation to be designated as an Approved Body was the UK affiliate of DEKRA almost a year ago. Prior to this, the only other UK Approved Bodies were three UK-designated Notified Bodies under the EU medical devices framework that had automatically converted to UK Approved Bodies following expiry of the Brexit transition period.
Industry had been expecting the appointment of a couple more UK Approved Bodies for some time and this is a welcome addition to the current fairly thin bench.
The update also follows the UK MDR amending legislation coming into force on 30 June 2023, which extended the transitional periods in the UK MDR. The deadlines for CE marked medical devices and IVDs to be commercialised in Great Britain (GB) have thus been extended to:
The increase in capacity to conduct UKCA conformity assessments will be welcome news for other UK Approved Bodies which, combined with the longer transition periods, will help clear the bottleneck to obtaining a UKCA mark. However, similar to when DEKRA’s UK affiliate was announced as an Approved Body, it is expected that the new Approved Bodies primarily use its UK designation to issue certificates allowing UKCA marking to its existing customers in the short term.
Click here to learn more about Medical Devices (Amendment) GB Regulations 2023.