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Directive 98/79/EC of the European Parliament and of the Council of 27 October 1998 on in vitro diagnostic medical devices
Annex I
Division B
Division 2

Division 2.6

United Kingdom

Original text. Later amendments are not shown.

Devices intended to be sterilised must be manufactured in appropriately controlled (e.g. environmental) conditions.

← Division 2.5

Division 2.6

Division 2.7 →

Legislation: Directive 98/79/EC of the European Parliament and of the Council of 27 October 1998 on in vitro diagnostic medical devices
Citation: EU Directive 1998/79, division 2.6
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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