# The Active Implantable Medical Devices Regulations 1992, Paragraph 3


The aim of surveillance is to ensure that the manufacturer duly fulfils the obligations which arise from the approved quality system.

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Source: https://www.legislation.gov.uk/uksi/1992/3146/schedule/8/paragraph/3 (the official version)
Page: https://openlegislation.uk/active-implantable-medical-devices-regulations-1992/schedule-8/paragraph-3
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.