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NF EN ISO 25539-2 : 2013

Withdrawn

Withdrawn

A Withdrawn Standard is one, which is removed from sale, and its unique number can no longer be used. The Standard can be withdrawn and not replaced, or it can be withdrawn and replaced by a Standard with a different number.

View Superseded by

CARDIOVASCULAR IMPLANTS - ENDOVASCULAR DEVICES - PART 2: VASCULAR STENTS

Withdrawn date

28-09-2014

Superseded by

NF EN ISO 25539-2:2020

Published date

12-01-2013

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La présente partie de l'ISO 25539 spécifie les exigences relatives aux stents vasculaires selon les connaissances médicales actuelles. En ce qui concerne la sécurité, elle donne les exigences relatives aux performances attendues, aux caractéristiques de conception, aux matériaux, à l'évaluation de la conception, à la fabrication, à la stérilisation, à l'emballage et aux informations fournies par le fabricant. Il convient de la considérer comme un complément à l'ISO 14630 qui spécifie les exigences générales relatives aux performances des implants chirurgicaux non actifs. Le domaine d'application inclut les stents utilisés dans le traitement des lésions vasculaires ou sténoses, ou d'autres anomalies vasculaires.

DevelopmentNote
Indice de classement: S94-203-2. PR NF EN ISO 25539-2 June 2007. (06/2007) PR NF EN ISO 25539-2 March 2009. (03/2009) Supersedes NF EN 12006-3. (04/2012) Supersedes NF EN 14299. (09/2014)
DocumentType
Standard
PublisherName
Association Francaise de Normalisation
Status
Withdrawn
SupersededBy

Standards Relationship
EN ISO 25539-2:2012 Identical
ISO 25539-2:2012 Identical

ISO 14630:2012 Non-active surgical implants — General requirements
ISO 14971:2007 Medical devices Application of risk management to medical devices

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