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Document 52002XC0731(03)

Commission Communication in the framework of the implementation of Council Directive 93/42/EEC of 14 June 1993 in relation to medical devices and Directive 98/79/EC of the European Parliament and of the Council of 27 October 1998 on in-vitro diagnostic medical devices (Text with EEA relevance)

OJ C 182, 31.7.2002, p. 8–8 (ES, DA, DE, EL, EN, FR, IT, NL, PT, FI, SV)

52002XC0731(03)

Commission Communication in the framework of the implementation of Council Directive 93/42/EEC of 14 June 1993 in relation to medical devices and Directive 98/79/EC of the European Parliament and of the Council of 27 October 1998 on in-vitro diagnostic medical devices (Text with EEA relevance)

Official Journal C 182 , 31/07/2002 P. 0008 - 0008


Commission Communication in the framework of the implementation of Council Directive 93/42/EEC of 14 June 1993 in relation to medical devices(1) and Directive 98/79/EC of the European Parliament and of the Council of 27 October 1998 on in-vitro diagnostic medical devices(2)

(2002/C 182/05)

(Text with EEA relevance)

(Publication of titles and references of harmonized standards under the Directive)

>TABLE>

Note 1:

Generally the date of cessation of presumption of conformity will be the date of withdrawal (dow), set by the European Standardisation Organisation, but attention of users of these standards is drawn to the fact that in certain exceptional cases this can be otherwise.

(1) OJ L 169, 12.7.1993, p. 1.

(2) OJ L 331, 7.12.1998, p. 1.

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