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ISO 25539-1 FRENCH

Implants cardiovasculaires - Dispositifs endovasculaires - Partie 1: Prothèses endovasculaires

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Organization: ISO
Publication Date: 1 February 2017
Status: active
Page Count: 140
ICS Code (Implants for surgery, prosthetics and orthotics): 11.040.40

Document History

ISO 25539-1 FRENCH
February 1, 2017
Implants cardiovasculaires - Dispositifs endovasculaires - Partie 1: Prothèses endovasculaires
A description is not available for this item.
ISO 25539-1 FRENCH
July 15, 2005
Implants cardiovasculaires - Dispositifs endovasculaires - Partie 1: Prothèses endovasculaires AMENDEMENT 1: Méthodes d'essai
A description is not available for this item.
ISO 25539-1 FRENCH
March 1, 2003
Implants cardiovasculaires - Dispositifs endovasculaires - Partie 1: Prothèses endovasculaires
A description is not available for this item.

References

This document references:
ISO 11607-2 - Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processes
Published by ISO on February 1, 2019
This document specifies requirements for the development and validation of processes for packaging medical devices that are terminally sterilized. These processes include forming, sealing and...
This document references:
ISO/IEC 17025 - General requirements for the competence of testing and calibration laboratories
Published by ISO on November 1, 2017
This document specifies the general requirements for the competence, impartiality and consistent operation of laboratories. This document is applicable to all organizations performing laboratory...
This document is referenced by:
ISO 5840-1 - Cardiovascular implants — Cardiac valve prostheses — Part 1: General requirements
Published by ISO on January 1, 2021
This document is applicable to heart valve substitutes intended for implantation and provides general requirements. Subsequent parts of the ISO 5840 series provide specific requirements. This...
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