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Information about medical devices that the public can buy for personal use and how we make sure they are safe and effective.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
What you need to do before your product can be placed on the Great Britain market with a UKCA mark.
Information for manufacturers of medical devices on post-market surveillance, reporting adverse incidents and field safety corrective actions to the MHRA.
How the MHRA makes decisions on whether a borderline product is a medical device and which risk class should apply.
How to register your medical devices with the MHRA for the markets in Great Britain and Northern Ireland.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
Updated MHRA guidance will help health institutions, such as NHS Trusts and Boards, safely design and make general medical devices for patients.
Information about how the MHRA regulates medical devices in Northern Ireland and what legislation applies to manufacturers and suppliers.
There are different regulations which apply to devices and equipment including hand gels and PPE (personal protective equipment)
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