The CE Marking is a crucial certification for medical devices sold within the European Union (EU) and European Economic Area (EEA). This mark is not only a legal requirement but also serves as a symbol of safety, quality, and regulatory compliance. CE marking assures that a product meets the strict health, safety, and environmental requirements of
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
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