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NF EN ISO 9713 : 2009

Superseded

Superseded

A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.

View Superseded by

NEUROSURGICAL IMPLANTS - SELF-CLOSING INTRACRANIAL ANEURYSM CLIPS

Published date

12-01-2013

Superseded date

31-03-2022

Superseded by

NF EN ISO 9713:2022

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1 Domaine d'application
2 Références normatives
3 Termes et définitions
4 Description des clips pour anévrisme
5 Indication des dimensions
6 Matériaux
7 Détermination des propriétés magnétiques
8 Force de fermeture
9 Marquage des clips
10 Stérilisation
11 Emballage
12 Étiquetage et documents d'accompagnement

Explains characteristics of self-closing aneurysm clips intended for permanent intracranial implantation and specifies requirements for their marking, packaging, sterilization and for labelling and accompanying documentation. In addition it gives a method for the measurement of closing force.

DevelopmentNote
Indice de classement: S94-302. (09/2004) PR NF EN ISO 9713 March 2009. (03/2009)
DocumentType
Standard
PublisherName
Association Francaise de Normalisation
Status
Superseded
SupersededBy

Standards Relationship
NEN EN ISO 9713 : 2010 Identical
I.S. EN ISO 9713:2009 Identical
NBN EN ISO 9713 : 2009 Identical
DIN EN ISO 9713:2009-08 Identical
NS EN ISO 9713 : 2009 Identical
EN ISO 9713:2009 Identical
BS EN ISO 9713:2009 Identical
ISO 9713:2002 Identical
UNE-EN ISO 9713:2009 Identical

ISO 5832-6:1997 Implants for surgery — Metallic materials — Part 6: Wrought cobalt-nickel-chromium-molybdenum alloy
ISO 5832-5:2005 Implants for surgery — Metallic materials — Part 5: Wrought cobalt-chromium-tungsten-nickel alloy
ISO 5832-3:2016 Implants for surgery — Metallic materials — Part 3: Wrought titanium 6-aluminium 4-vanadium alloy
ISO 5832-8:1997 Implants for surgery — Metallic materials — Part 8: Wrought cobalt-nickel-chromium-molybdenum- tungsten-iron alloy
ISO 14630:2012 Non-active surgical implants — General requirements
ISO 16061:2015 Instrumentation for use in association with non-active surgical implants — General requirements
ISO 5832-2:1999 Implants for surgery — Metallic materials — Part 2: Unalloyed titanium
ISO 5832-7:2016 Implants for surgery — Metallic materials — Part 7: Forgeable and cold-formed cobalt-chromium-nickel-molybdenum-iron alloy
ISO 15223:2000 Medical devices — Symbols to be used with medical device labels, labelling and information to be supplied

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