# The Active Implantable Medical Devices Regulations 1992, Paragraph 6: Modifications


The relevant notified body—
(a) shall withdraw any EC type-examination certificate or supplementary approval given by it if it considers that the device no longer conforms with the relevant essential requirements or the conditions of use specified for the device; and
(b) may withdraw the EC type-examination certificate or supplementary approval if it has been given on the basis of false or misleading information.

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Source: https://www.legislation.gov.uk/uksi/1992/3146/schedule/6/paragraph/6 (the official version)
Page: https://openlegislation.uk/active-implantable-medical-devices-regulations-1992/schedule-6/paragraph-6
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.