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 in the UK, un… Read More


The CE Mark (Conformité Européenne) is a critical certification for medical devices sold in the European Union (EU) and the European Economic Area (EEA). It signifies that a product meets the stringent health, safety, and environmental standards set by the European regulatory authorities. This mark is not only a legal requirement but also serves … Read More


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