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BSI - BS ISO 15674

Cardiovascular implants and artificial organs - Hard-shell cardiotomy/venous reservoir systems (with/without filter) and soft venous reservoir bags

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Organization: BSI
Publication Date: 30 November 2009
Status: inactive
Page Count: 18
ICS Code (Implants for surgery, prosthetics and orthotics): 11.040.40

Document History

BS ISO 15674
August 31, 2016
Cardiovascular implants and artificial organs - Hard-shell cardiotomy/venous reservoir systems (with/without filter) and soft venous reservoir bags
A description is not available for this item.
BS ISO 15674
August 31, 2016
Cardiovascular implants and artificial organs - Hard-shell cardiotomy/venous reservoir systems (with/without filter) and soft venous reservoir bags
A description is not available for this item.
BS ISO 15674
November 30, 2009
Cardiovascular implants and artificial organs - Hard-shell cardiotomy/venous reservoir systems (with/without filter) and soft venous reservoir bags
A description is not available for this item.
BS ISO 15674
November 26, 2001
Cardiovascular Implants and Artificial Organs - Hard-Shell Cardiotomy/Venous Reservoir Systems (with/without Filter) and Soft Venous Reservoir Bags
A description is not available for this item.

References

This document references:
ISO 7199 - Cardiovascular implants and artificial organs - Blood-gas exchangers (oxygenators)
Published by ISO on November 15, 2016
This document specifies requirements for sterile, single-use, extracorporeal blood-gas exchangers (oxygenators) intended for supply of oxygen to, and removal of carbon dioxide from, the blood of...
This document references:
ISO 17665-1 - Sterilization of health care products Moist heat Part 1: Requirements for the development, validation and routine control of a sterilization process for medical devices
Published by ISO on August 15, 2006
Inclusions This part of ISO 17665 specifies requirements for the development, validation and routine control of a moist heat sterilization process for medical devices. NOTE Although the scope of this...
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:
11607-1 AMD 1 - Packaging for terminally sterilized medical devices — Part 1: Requirements for materials, sterile barrier systems and packaging systems AMENDMENT 1: Application of risk management
Published by ISO on September 1, 2023
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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