# The Active Implantable Medical Devices Regulations 1992, Paragraph 2: General requirements


The device must achieve the performances intended by its manufacturer and, in particular, must be designed and manufactured in such a way that it is suitable for one or more of the following functions as specified by him:—
(a) diagnosis, prevention, monitoring, treatment or alleviation of disease or injury;
(b) investigation, replacement or modification of the anatomy or of a physiological process;
(c) control of conception.

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Source: https://www.legislation.gov.uk/uksi/1992/3146/schedule/2/paragraph/2 (the official version)
Page: https://openlegislation.uk/active-implantable-medical-devices-regulations-1992/schedule-2/paragraph-2
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.