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
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 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
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
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