About UK RepMed

UK Rep Med acts as a UK Responsible person for Medical Device Manufacturers. This is also know as an Authorised Representative or UK Rep. This is now a requirement by the MHRA (UK Competent Health Authority). All Medical Device manufacturers who are based outside the UK and want to continue to export to the UK must have their Medical Devices registered with the MHRA by a UK Responsible Person.

UK Rep Med Limited is a UK based company that provides and deals with regulatory registration requirements in the international industry of medical components for medical product manufacturers based outside the UK.

If you are a manufacturer located outside the UK, but selling into the UK market, there are many potential benefits to appointing UK Rep Med Limited as your UK Responsible Person.

We can ensure that you meet all your legal obligations under UK regulations that apply to your products, minimising risk. We can respond with knowledge to queries from the authorities or other third-parties when they arise. We can keep you up-to-date on regulatory changes to ensure your products remain compliant.

Our experienced consultants will review your Technical File, register your medical device, as required, and respond to any questions or concerns from the Competent Authorities and or the MHRA.

You will have secure access to all your documentation and regulatory information, including technical files, labelling information and symbols, language requirements, directives, and guidelines

Our vast expertise with European regulations, facilitates a smooth and efficient registration process.

We will send frequent updates to all our represented clients with important regulatory updates focused on the UK

You will have secure access to all your documentation and regulatory information, including technical files, labelling information and symbols, language requirements, directives, and guidelines

Our vast expertise with European regulations, facilitates a smooth and efficient registration process.

We will send frequent updates to all our represented clients with important regulatory updates focused on the UK