EN 13612:2002/AC:2002
(Corrigendum)Performance evaluation of in vitro diagnostic medical devices
Performance evaluation of in vitro diagnostic medical devices
TC - Modifications in 2.6, 2.14, 4.5, Annex ZA and Bibliography
Leistungsbewertung von In-vitro-Diagnostika
Détermination des performances des dispositifs médicaux pour diagnostic in vitro
Ovrednotenje diagnostičnih medicinskih pripomočkov lastnosti in vitro
General Information
Relations
Frequently Asked Questions
EN 13612:2002/AC:2002 is a corrigendum published by the European Committee for Standardization (CEN). Its full title is "Performance evaluation of in vitro diagnostic medical devices". This standard covers: TC - Modifications in 2.6, 2.14, 4.5, Annex ZA and Bibliography
TC - Modifications in 2.6, 2.14, 4.5, Annex ZA and Bibliography
EN 13612:2002/AC:2002 is classified under the following ICS (International Classification for Standards) categories: 11.100 - Laboratory medicine. The ICS classification helps identify the subject area and facilitates finding related standards.
EN 13612:2002/AC:2002 has the following relationships with other standards: It is inter standard links to EN 13612:2002. Understanding these relationships helps ensure you are using the most current and applicable version of the standard.
EN 13612:2002/AC:2002 is associated with the following European legislation: EU Directives/Regulations: 98/79/EC. When a standard is cited in the Official Journal of the European Union, products manufactured in conformity with it benefit from a presumption of conformity with the essential requirements of the corresponding EU directive or regulation.
You can purchase EN 13612:2002/AC:2002 directly from iTeh Standards. The document is available in PDF format and is delivered instantly after payment. Add the standard to your cart and complete the secure checkout process. iTeh Standards is an authorized distributor of CEN standards.
Standards Content (Sample)
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.LWURLeistungsbewertung von In-vitro-DiagnostikaDétermination des performances des dispositifs médicaux pour diagnostic in vitroPerformance evaluation of in vitro diagnostic medical devices11.100.10In vitro diagnostic test systemsICS:Ta slovenski standard je istoveten z:EN 13612:2002/AC:2002SIST EN 13612:2002/AC:2003en01-marec-2003SIST EN 13612:2002/AC:2003SLOVENSKI
STANDARD
EUROPEAN STANDARDNORME EUROPÉENNEEUROPÄISCHE NORMEN 13612:2002/ACDecember 2002Décembre 2002Dezember 2002ICS 11.100English versionVersion FrançaiseDeutsche FassungPerformance evaluation of in vitro diagnostic medical devicesDétermination des performances des dispositifs médicaux pourdiagnostic in vitroLeistungsbewertung von In-vitro-DiagnostikaThis corrigendum becomes effective on 18 December 2002 for incorporation in the three officiallanguage versions of the EN.Ce corrigendum prendra effet le 18 décembre 2002 pour incorporation dans les trois versionslinguistiques officielles de l'EN.Die Berichtigung tritt am 18. Dezember 2002 zur Einarbeitung in die drei offiziellen Sprachfassungender EN in Kraft.EUROPEAN COMMITTEE FOR STANDARDIZATIONCOMITÉ EUROPÉEN DE NORMALISATIONEUROPÄISCHES KOMITEE FÜR NORMUNGManagement Centre: rue de Stassart, 36
B-1050 Brussels© 2002 CENAll rights of exploitation in any form and by any means reserved worldwide for CEN national Members.Tous droits d'exploitation sous quelque forme et de quelque manière que ce soit réservés dans le monde entier auxmembres nationaux du CEN.Alle Rechte der Verwertung, gleich in welcher Form und in welchem Verfahren, sind weltweit den nationalen Mitgliedernvon CEN vorbehalten.Ref. No. EN 13612:2002/AC:2002 D/E/FSIST EN 13612:2002/AC:2003
"[EN ISO 9000:2000, 3.8.5]"4.5
Experimental designIn the 14 th dash "expected" has to be replaced by "unexpected" as follows:– availability of additional information concerning the specimen or donor if follow-up ofunexpected results is required;Annex ZA (informative) - Clauses of this European Standard addressing essentialrequirements or other provisions of EU Directives"EU" has to be deleted three times as follows:The following clauses of this standard, as detailed in Table ZA.1, are likely to support requirements ofthe EU Directive 98/79/EC.Table ZA.1 - Correspondence between this European Standard and EU Directive 98/79/ECClauses/subclauses of thisEuropean StandardEssential requirements of EUDirective 98/79/ECQualifying remarks/notesBibliographyThe refenences list has to be re-organized to the following order "ENs, EN ISOs, ISOs, otherdocuments" and the chan
...
The article EN 13612:2002/AC:2002 discusses modifications made to various sections of the performance evaluation of in vitro diagnostic medical devices. These modifications include changes in sections 2.6, 2.14, 4.5, Annex ZA, and the Bibliography.








Questions, Comments and Discussion
Ask us and Technical Secretary will try to provide an answer. You can facilitate discussion about the standard in here.
Loading comments...