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.
Guidance for healthcare professionals on managing specific medicines and medical devices and using them safely.
Order a certificate of free sale to export medical devices outside the UK.
How a manufacturer can apply for approval to supply a non-compliant medical device on humanitarian grounds.
List of manufacturers and their medical devices granted an exemption by MHRA. The list also includes manufacturers whose exemption expired or was cancelled.
Information on when software applications are considered to be a medical device and how they are regulated.
Checklists providing a practical guide to using medical devices.
The MHRA has conducted a thorough assessment of technical and biological safety information provided by NSO and is satisfied that the modified MAGEC X system can now be used in the UK.
Home Office approved drug-testing devices.
Guidance on what approved bodies are, what they do and how you can become one.
The MHRA welcomes the publication of Dame Margaret Whitehead’s Equity in Medical Devices: Independent Review
We're looking for your views on how medical devices will be regulated across the United Kingdom (UK) in the future.
UK approved bodies listed under Medical Devices Regulations 2002 (SI 2002 No 618, as amended) (UK MDR 2002).
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...
Guidance to help you manage the security of your devices and help protect your privacy
Guidance for organisations when making decisions about the design and operation of enterprise IT services which handle OFFICIAL information.
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.
Guidance for manufacturers who don’t design or manufacture devices but place their names on the product.
Posters and leaflets about using medical devices safely for healthcare professionals.
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).