List of UK Approved Bodies for Medical Devices
In the UK, medical devices must be assessed and certified by an UK Approved Body before they can be marketed in the territory.
A UK Approved Body is an organisation designated by the UK health authority, the Medicines and Healthcare products Regulatory Agency – or MHRA – to assess whether manufacturers and their medical devices meet the required standards set out in the UK Medical Devices Regulations 2002 – also known as UK MDR 2002. They are responsible for certification, which allows manufacturers to place the UKCA marking on their products, thereby permitting them to be sold in England, Wales, and Scotland
Approved Bodies carry out various tasks depending on the classification of the products concerned. But typically, the role encompasses
Manufacturers looking for a UK Approved Body to certify their medical devices can find a list of approved bodies based in the UK below.
Below is a list of UK Approved Bodies that have been designated to assess and certify medical devices in accordance with the UK MDR 2002. These bodies have been accredited by the Medicines and Healthcare products Regulatory Agency (MHRA) and are regularly monitored to ensure they continue to meet the requirements for designation.
EU MDR (Medical Device Regulation)
Differences between UK MDR and EU MDR
Do you sell medical devices in the UK? Medical Devices manufacturers require a UK Authorised Representative to sell in the UK.
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