The UKCA (UK Conformity Assessed) Marking has become a mandatory requirement for all medical devices sold in the United Kingdom, effective from January 1, 2023. This shift marks the transition from the previously accepted CE certification to the UKCA marking, as the UK establishes its regulatory framework post-Brexit. For manufacturers https://dnatestingservices49360.blogginaway.com/32001443/understanding-ukca-marking-for-medical-devices-key-insights-for-manufacturers