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Council Directive 93/42/EEC of 14 June 1993 concerning medical devices
Annex I
Division II
Division 8

Division 8.7

United Kingdom

Original text. Later amendments are not shown.

The packaging and/or label of the device must distinguish between identical or similar products sold in both sterile and non-sterile condition.

← Division 8.6

Division 8.7

Legislation: Council Directive 93/42/EEC of 14 June 1993 concerning medical devices
Citation: EU Directive 1993/42, division 8.7
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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