As Of January 1, 2023, the UKCA (UK Conformity Assessed) marking is mandatory for all medical devices sold in the United Kingdom. This change represents a significant shift from the previously accepted CE certification, with the UK establishing its regulatory framework following Brexit. For manufacturers aiming to sell medical devices https://dna-testing-services19741.thelateblog.com/31945585/understanding-ukca-marking-for-medical-devices-key-insights-for-manufacturers