We use some essential cookies to make this website work.
We’d like to set additional cookies to understand how you use GOV.UK, remember your settings and improve government services.
We also use cookies set by other sites to help us deliver content from their services.
You have accepted additional cookies. You can change your cookie settings at any time.
You have rejected additional cookies. You can change your cookie settings at any time.
Departments, agencies and public bodies
News stories, speeches, letters and notices
Detailed guidance, regulations and rules
Reports, analysis and official statistics
Consultations and strategy
Data, Freedom of Information releases and corporate reports
Register to vote Register by 18 June to vote in the General Election on 4 July.
The Devices Expert Advisory Committee (DEAC) replaces the Committee on Safety of Devices and is responsible for providing independent, external expert input and advice on a wide range of aspects relating to medical devices to help the Medicines and Healthcare...
Anti-choking devices are intended to alleviate choking incidents after Basic Life Support protocols have been attempted and failed. There are numerous counterfeit and unbranded anti-choking devices being sold in the UK online which do not have a valid UKCA or...
Guidance for manufacturers who don’t design or manufacture devices but place their names on the product.
Home Office approved drug-testing devices.
Report on all regulations in force during the first reporting period made using the powers in specific sections of the act, including stakeholder feedback and the department’s response.
Information to support commercial fishers on under 12 metre English vessels.
Guidance on whether or not your product is a medical device.
How the supply of medical devices from Great Britain into Northern Ireland works.
Using retractable or foldable aerodynamic rear devices on heavy goods vehicles.
We're looking for your views on how medical devices will be regulated across the United Kingdom (UK) in the future.
Guidance on defining intended purpose for Software as a Medical Device (SaMD), to help SaMD manufacturers in meeting their statutory obligations.
The Interim Devices Working Group replaces the Devices Expert Advisory Committee (DEAC) and is responsible for providing independent, external expert input and advice on a wide range of aspects relating to medical devices to help MHRA ensure the safe introduction...
The Medicines and Healthcare products Regulatory Agency (MHRA) has today (21 May 2024) launched a four-week consultation which will support improved safety for certain high risk in vitro diagnostic (IVD) devices.
Guidance on what approved bodies are, what they do and how you can become one.
Notices of publication and a consolidated list for designated standards for active implantable medical devices.
Don’t include personal or financial information like your National Insurance number or credit card details.
To help us improve GOV.UK, we’d like to know more about your visit today. Please fill in this survey (opens in a new tab).