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Document 52008XC0723(04)
Commission communication in the framework of the implementation of the Directive 98/79/EC of the European Parliament and of the Council on in vitro diagnostic medical devices (Text with EEA relevance)
Commission communication in the framework of the implementation of the Directive 98/79/EC of the European Parliament and of the Council on in vitro diagnostic medical devices (Text with EEA relevance)
Commission communication in the framework of the implementation of the Directive 98/79/EC of the European Parliament and of the Council on in vitro diagnostic medical devices (Text with EEA relevance)
SL C 186, 23.7.2008, p. 25–27
(BG, ES, CS, DA, DE, ET, EL, EN, FR, IT, LV, LT, HU, MT, NL, PL, PT, RO, SK, SL, FI, SV)
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23.7.2008 |
EN |
Official Journal of the European Union |
C 186/25 |
Commission communication in the framework of the implementation of the Directive 98/79/EC of the European Parliament and of the Council on in vitro diagnostic medical devices
(Text with EEA relevance)
(Publication of titles and references of harmonised standards under the directive)
(2008/C 186/08)
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ESO (1) |
Reference and title of the harmonised standard (and reference document) |
Reference of superseded standard |
Date of cessation of presumption of conformity of superseded standard (Note 1) |
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CEN |
EN 375:2001 Information supplied by the manufacturer with in vitro diagnostic reagents for professional use |
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CEN |
EN 376:2002 Information supplied by the manufacturer with in vitro diagnostic reagents for self-testing |
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CEN |
EN 556-1:2001 Sterilization of medical devices — Requirements for medical devices to be designated ‘STERILE’ — Part 1: Requirements for terminally sterilized medical devices |
EN 556:1994 + A1:1998 |
Date expired (30.4.2002) |
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EN 556-1:2001/AC:2006 |
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CEN |
EN 556-2:2003 Sterilization of medical devices — Requirements for medical devices to be designated ‘STERILE’ — Part 2: Requirements for aseptically processed medical devices |
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CEN |
EN 591:2001 Instructions for use for in vitro diagnostic instruments for professional use |
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CEN |
EN 592:2002 Instructions for use for in vitro diagnostic instruments for self-testing |
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CEN |
EN 980:2008 Symbols for use in the labelling of medical devices |
EN 980:2003 |
31.5.2010 |
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CEN |
EN 12286:1998 In vitro diagnostic medical devices — Measurement of quantities in samples of biological origin — Presentation of reference measurement procedures |
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EN 12286:1998/A1:2000 |
Note 3 |
Date expired (24.11.2000) |
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CEN |
EN 12287:1999 In vitro diagnostic medical devices — Measurement of quantities in samples of biological origin — Description of reference materials |
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CEN |
EN 12322:1999 In vitro diagnostic medical devices — Culture media for microbiology — Performance criteria for culture media |
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EN 12322:1999/A1:2001 |
Note 3 |
Date expired (30.4.2002) |
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CEN |
EN ISO 13485:2003 Medical devices — Quality management systems — Requirements for regulatory purposes (ISO 13485:2003) |
EN 46003:1999 EN ISO 13485:2000 EN ISO 13488:2000 |
31.7.2009 |
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EN ISO 13485:2003/AC:2007 |
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CEN |
EN 13532:2002 General requirements for in vitro diagnostic medical devices for self-testing |
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CEN |
EN 13612:2002 Performance evaluation of in vitro diagnostic medical devices |
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CEN |
EN 13640:2002 Stability testing of in vitro diagnostic reagents |
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CEN |
EN 13641:2002 Elimination or reduction of risk of infection related to in vitro diagnostic reagents |
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CEN |
EN 13975:2003 Sampling procedures used for acceptance testing of in vitro diagnostic medical devices — Statistical aspects |
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CEN |
EN 14136:2004 Use of external quality assessment schemes in the assessment of the performance of in vitro diagnostic examination procedures |
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CEN |
EN 14254:2004 In vitro diagnostic medical devices — Single-use receptacles for the collection of specimens, other than blood, from humans |
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CEN |
EN 14820:2004 Single-use containers for human venous blood specimen collection |
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CEN |
EN ISO 14937:2000 Sterilization of health care products — General requirements for characterization of a sterilizing agent and the development, validation and routine control of a sterilization process for medical devices (ISO 14937:2000) |
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CEN |
EN ISO 14971:2007 Medical devices — Application of risk management to medical devices (ISO 14971:2007) |
EN ISO 14971:2000 |
31.3.2010 |
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CEN |
EN ISO 15197:2003 In vitro diagnostic test systems — Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus (ISO 15197:2003) |
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CEN |
EN ISO 15225:2000 Nomenclature — Specification for a nomenclature system for medical devices for the purpose of regulatory data exchange (ISO 15225:2000) |
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CEN |
EN ISO 17511:2003 In vitro diagnostic medical devices — Measurement of quantities in biological samples — Metrological traceability of values assigned to calibrators and control materials (ISO 17511:2003) |
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CEN |
EN ISO 18153:2003 In vitro diagnostic medical devices — Measurement of quantities in biological samples — Metrological traceability of values for catalytic concentration of enzymes assigned to calibrators and control materials (ISO 18153:2003) |
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CEN |
EN ISO 20776-1:2006 Clinical laboratory testing and in vitro diagnostic test systems — Susceptibility testing of infectious agents and evaluation of performance of antimicrobial susceptibility test devices — Part 1: Reference method for testing the in vitro activity of antimicrobial agents against rapidly growing aerobic bacteria involved in infectious diseases (ISO 20776-1:2006) |
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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. |
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Note 3 |
In case of amendments, the referenced standard is EN CCCCC:YYYY, its previous amendments, if any, and the new, quoted amendment. The superseded standard (column 3) therefore consists of EN CCCCC:YYYY and its previous amendments, if any, but without the new quoted amendment. On the date stated, the superseded standard ceases to give presumption of conformity with the essential requirements of the directive. |
Note:
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Any information concerning the availability of the standards can be obtained either from the European Standardisation Organisations or from the national standardisation bodies of which the list is annexed to the Directive 98/34/EC of the European Parliament and of the Council (2) amended by the Directive 98/48/EC (3). |
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Publication of the references in the Official Journal of the European Union does not imply that the standards are available in all the Community languages. |
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This list replaces all the previous lists published in the Official Journal of the European Union. The Commission ensures the updating of this list. |
More information about harmonised standards on the Internet at:
http://ec.europa.eu/enterprise/newapproach/standardization/harmstds/
(1) ESO: European Standardisation Organisation:
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CEN: rue de Stassart 36, B-1050 Brussels, Tel. (32-2) 550 08 11; fax (32-2) 550 08 19 (http://www.cen.eu) |
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Cenelec: rue de Stassart 35, B-1050 Brussels, Tel. (32-2) 519 68 71; fax (32-2) 519 69 19 (http://www.cenelec.org) |
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ETSI: 650, route des Lucioles, F-06921 Sophia Antipolis, Tel. (33) 492 94 42 00; fax (33) 493 65 47 16 (http://www.etsi.org). |
(2) OJ L 204, 21.7.1998, p. 37.
(3) OJ L 217, 5.8.1998, p. 18.