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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.
Guidance for manufacturers who don’t design or manufacture devices but place their names on the product.
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 on whether or not your product is a medical device.
Home Office approved drug-testing devices.
Information to support commercial fishers on under 12 metre English vessels.
Using retractable or foldable aerodynamic rear devices on heavy goods vehicles.
How the supply of medical devices from Great Britain into Northern Ireland works.
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.
Guidance for manufacturers on the regulations that apply to prosthetic, orthotic and ophthalmic devices.
Notices of publication and a consolidated list for designated standards for active implantable medical devices.
Guidance on what approved bodies are, what they do and how you can become one.
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...
Service providers or government departments installing networking technologies in government shared buildings, known as hub buildings.
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