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Device Bulletins

Device Bulletins contain guidance and information on medical devices of a more general management interest. They are written as a result of experience gained from adverse incident investigations, our contacts with manufacturers and users, and other sources of information.

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NHS Evidence has accredited the process used by the Medicines and Healthcare products Regulatory Agency (MHRA) to produce Device Bulletins. Accreditation is valid for three years from September 2010 and is retrospectively applicable to guidance produced from September 2007. More information on accreditation can be viewed on the NHS Evidence website (external link).

Latest device bulletins


Page last modified: 12 January 2012