# The Active Implantable Medical Devices Regulations 1992, Paragraph 4: General requirements


The device shall be designed, manufactured and packed in such a way that its characteristics and performances are not adversely affected if the conditions as to storage and transport laid down by the manufacturer, such as conditions relating to temperature or humidity, are met.

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Source: https://www.legislation.gov.uk/uksi/1992/3146/schedule/2/paragraph/4 (the official version)
Page: https://openlegislation.uk/active-implantable-medical-devices-regulations-1992/schedule-2/paragraph-4
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.