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From CE to UKCA: Navigating the UK Medical Device Transition
This episode breaks down the essential steps for medical device manufacturers with a CE mark to comply with UK regulations for Great Britain. We cover the extended deadlines for CE mark recognition, the immediate requirements for MHRA registration and appointing a UK Responsible Person (UKRP), and the process for achieving UKCA conformity assessment. Learn the key dates and actions you need to take to ensure uninterrupted market access. Key Questions: • Is my CE mark still valid for selling medical devices in Great Britain? • What are the new deadlines for transitioning from CE to UKCA…
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