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The Active Implantable Medical Devices Regulations 1992
Schedule 8
Part II

Paragraph 3

Original text. Later amendments are not shown.

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

← Paragraph 2

Paragraph 3

Paragraph 4 →

Legislation: The Active Implantable Medical Devices Regulations 1992
Citation: S.I. 1992/3146, paragraph 3
Official version: legislation.gov.uk

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Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives. legislation.gov.uk is the official version.

Not legal advice.

👋 Jason Cartwright
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