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
Guidance for organisations when making decisions about the design and operation of enterprise IT services which handle OFFICIAL information.
What to do if a laptop or tablet you’ve received from a DfE programme is not working.
A buyer's guide for mobile devices, which outlines 7 areas that consumers should check for when choosing or using their mobile device.
Order a certificate of free sale to export medical devices outside the UK.
Information on road traffic devices, such as breath-testing, speed cameras and immobilisation devices.
Research detailing cyber security issues in internet-connected devices used by businesses and organisations.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
How a manufacturer can apply for approval to supply a non-compliant medical device on humanitarian grounds.
Product security factsheet accompanying the Product Security and Telecommunications Infrastructure Bill, outlining the problems the Bill will address and how.
There are a number of high cost devices that are excluded from the Payment by Results (PbR) tariff.
Medicines and Healthcare products Regulatory Agency (MHRA) guidance on using medical devices safely.
UK approved bodies listed under Medical Devices Regulations 2002 (SI 2002 No 618, as amended) (UK MDR 2002).
Advice on writing clear notices and maximising replies to your FSNs.
For waste operators and exporters classifying some waste electrical and electronic equipment (WEEE) devices, waste components, and wastes from their treatment.
The requirements for 3D printed products will depend on whether they are classed as medical devices, personal protective equipment (PPE) or both.
Guidance for healthcare professionals covers the use, management and safety of in vitro diagnostic (IVD) devices, including blood glucose meters.
Information on when software applications are considered to be a medical device and how they are regulated.
Posters and leaflets about using medical devices safely for healthcare professionals.
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...
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. We’ll send you a link to a feedback form. It will take only 2 minutes to fill in. Don’t worry we won’t send you spam or share your email address with anyone.