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 covers the use, management and safety of in vitro diagnostic (IVD) devices, including blood glucose meters.
Guidance on defining intended purpose for Software as a Medical Device (SaMD), to help SaMD manufacturers in meeting their statutory obligations.
Guidance on whether or not your product is a medical device.
Guidance explaining the main features of the Medical Devices Regulations 2002 (SI 2002 No 618, as amended) in relation to in vitro diagnostic medical devices
Notices of publication and a consolidated list for designated standards for medical devices.
A buyer's guide for mobile devices, which outlines 7 areas that consumers should check for when choosing or using their mobile device.
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...
Information about who could get devices from the Get Help with Technology programme and how devices were allocated to disadvantaged children and young people.
What to do if a laptop or tablet you’ve received from a DfE programme is not working.
This document is an update of an original Department for Transport document, "The Certification of Approved Devices", to cover road user charging applications.
Detention services order 05/2014 about the installation and removal of electronic monitoring devices from detainees.
Guidance for manufacturers on the regulations that apply to prosthetic, orthotic and ophthalmic devices.
Information for manufacturers, healthcare professionals, researchers and patients on software as a medical device (SaMD) and AI as a medical device (AIaMD).
List of certifications granted by the Secretary of State for Transport for approved devices, CCTV and associated evidence-recording equipment.
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).