The Steps Needed to Export a Medical Device to the UK and the role of the UK Responsible Person

For someone from outside the UK, exporting a medical device into the country can be a daunting task. In this blog post, we will discuss the necessary steps needed to export a medical device to the UK, including the role of the UK Responsible Person.

Step 1: Classify the Medical Device.

Before exporting a medical device to the UK, you need to classify it based on its intended use, design, and mode of operation. The classification will determine the type of conformity assessment required, and therefore, the rules you’ll need to comply with. The UK Medical and Healthcare Products Regulatory Agency (MHRA) regulates medical devices in the UK. The MHRA classifies medical devices based on the current CE categories: Class I, IIa, IIb, and III.

Step 2: Appoint a UK Responsible Person.

A UK Responsible Person (UKRP) is a designated person or organization responsible for ensuring that a medical device complies with UK regulations and requirements. The UKRP could be the manufacturer, importer, or distributor. If you’re an exporter, you need to ensure that your medical device has a UKRP, as it is a UK legal requirement. A UKRP must have a physical presence in the UK and be knowledgeable about UK regulations and requirements. The UKRP will need to register with the MHRA and provide the device’s CE Certificate

Step 3: Obtain a Conformity Assessment Certificate.

Before importing medical devices into the UK, you’ll need a conformity assessment certificate (CE). The certificate confirms that the device meets UK regulations and standards. The certificate can be issued by a notified body, which is an organization designated by the MHRA to assess medical devices’ conformity. The notified body will review your device’s technical documentation, conduct tests, and issue a conformity assessment certificate if it complies with UK regulations and standards.

Step 4: Register the Medical Device.

All medical devices imported into the UK need to be registered with the MHRA. The registration process involves providing details about the device, its manufacturer, UK Responsible Person, and conformity assessment certificate. The registration must be carried out by the UKRP

Step 5: Ensure Compliance with UK Regulations.

After registering your medical device, you need to ensure that it complies with UK regulations and standards. The UKRP will need to monitor the device’s performance, report any adverse events to the MHRA, and ensure that any changes made to the device comply with UK regulations. Compliance with UK regulations will ensure that your device remains on the UK market and continues to meet safety and effectiveness standards.


Exporting a medical device to the UK requires careful planning and adherence to regulations and requirements. You’ll need to classify the device, appoint a UKRP, obtain a conformity assessment certificate, register the device, and ensure compliance with UK regulations. The UKRP plays a crucial role in ensuring that the device complies with UK regulations and standards. By following these steps, you can successfully export your medical device to the UK and contribute to improving patient healthcare.

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