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 seeking to a
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
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