While there are no specific obligations for distributors in the UK Medical Device Regulations, it would be an offence under the UK regulations to supply a medical device that does not meet the UK’s requirements.
It is advisable therefore, for anyone intending to distribute medical devices in the UK, to be familiar with the regulations that apply and to first verify the device concerned is compliant.
All medical devices intended for the GB and NI markets must display the name and address of a UK manufacturer, or a UK responsible person or an EU authorised representative. Whichever is the case, that individual or company should be able to confirm to a prospective distributor that the device concerned complies with the UK’s regulations.