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BSI - BS ISO 15675

Cardiovascular implants and artificial organs - Cardiopulmonary bypass systems - Arterial blood line filters

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Organization: BSI
Publication Date: 31 August 2016
Status: inactive
Page Count: 18
ICS Code (Implants for surgery, prosthetics and orthotics): 11.040.40

Document History

BS ISO 15675
August 31, 2016
Cardiovascular implants and artificial organs - Cardiopulmonary bypass systems - Arterial blood line filters
A description is not available for this item.
BS ISO 15675
August 31, 2016
Cardiovascular implants and artificial organs - Cardiopulmonary bypass systems - Arterial blood line filters
A description is not available for this item.
BS ISO 15675
November 30, 2009
Cardiovascular implants and artificial organs - Cardiopulmonary bypass systems - Arterial blood line filters
A description is not available for this item.
BS ISO 15675
November 1, 2001
Cardiovascular Implants and Artificial Organs - Cardiopulmonary Bypass Systems - Arterial Line Blood Filters
A description is not available for this item.

References

This document references:
ISO 10993-1 - Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process
Published by ISO on August 1, 2018
This document specifies: — the general principles governing the biological evaluation of medical devices within a risk management process; — the general categorization of medical devices based on the...
This document references:
ISO 10993-11 - Biological evaluation of medical devices - Part 11: Tests for systemic toxicity
Published by ISO on September 1, 2017
This document specifies requirements and gives guidance on procedures to be followed in the evaluation of the potential for medical device materials to cause adverse systemic reactions.
This document references:
ISO 10993-1 FRENCH - Évaluation biologique des dispositifs médicaux - Partie 1: Évaluation et essais au sein d'un processus de gestion du risque
Published by ISO on August 1, 2018
A description is not available for this item.
This document references:
ISO 10993-11 FRENCH - Évaluation biologique des dispositifs médicaux - Partie 11: Essais de toxicité systémique
Published by ISO on September 1, 2017
A description is not available for this item.
This document references:
ISO 11135 - Sterilization of health-care products - Ethylene oxide - Requirements for the development, validation and routine control of a sterilization process for medical devices
Published by ISO on July 15, 2014
Inclusions This International Standard specifies requirements for the development, validation and routine control of an ethylene oxide sterilization process for medical devices in both the industrial...
This document is referenced by:
BS ISO 11658 - Cardiovascular implants and extracorporeal systems - Blood/tissue contact surface modifications for extracorporeal perfusion systems
Published by BSI on May 31, 2012
A description is not available for this item.
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