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BSI - BS EN ISO 7199

Cardiovascular implants and artificial organs - Blood-gas exchangers (oxygenators)

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Organization: BSI
Publication Date: 31 January 2017
Status: active
Page Count: 36
ICS Code (Implants for surgery, prosthetics and orthotics): 11.040.40

Document History

BS EN ISO 7199
January 31, 2017
Cardiovascular implants and artificial organs - Blood-gas exchangers (oxygenators)
A description is not available for this item.
BS EN ISO 7199
January 31, 2017
Cardiovascular implants and artificial organs - Blood-gas exchangers (oxygenators)
A description is not available for this item.
BS ISO 7199
November 30, 2009
Cardiovascular implants and artificial organs - Blood-gas exchangers (oxygenators)
A description is not available for this item.
BS ISO 7199
November 30, 2009
Cardiovascular implants and artificial organs - Blood-gas exchangers (oxygenators)
A description is not available for this item.
BS EN ISO 7199
November 30, 2009
Cardiovascular implants and artificial organs - Blood-gas exchangers (oxygenators)
A description is not available for this item.

References

This document references:
ISO 15675 - Cardiovascular implants and artificial organs — Cardiopulmonary bypass systems — Arterial blood line filters AMENDMENT 1: Connectors
Published by ISO on February 1, 2020
A description is not available for this item.
This document references:
ISO TS 23810 - Cardiovascular implants and artificial organs - Checklists for use of extracorporeal circulation equipment
Published by ISO on July 1, 2018
This document covers the activities performed by perfusionists before, during, and after extracorporeal circulation. Clause 4 covers the perfusionists’ actions during preoperative extracorporeal...
This document references:
BS EN ISO 11607-2 - Packaging for terminally sterilized medical devices Part 2: Validation requirements for forming, sealing and assembly processes
Published by BSI on January 31, 2020
A description is not available for this item.
This document references:
BS EN ISO 14971 + A11 - Medical devices - Application of risk management to medical devices
Published by BSI on December 31, 2019
A description is not available for this item.
This document references:
BS EN ISO 11137-1 - Sterilization of health care products — Radiation Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices
Published by BSI on July 31, 2015
A description is not available for this item.
This document is referenced by:
BS EN ISO 10993-4 - Biological evaluation of medical devices Part 4: Selection of tests for interactions with blood
Published by BSI on May 31, 2017
A description is not available for this item.
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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