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BSI - BS EN ISO 25539-1

Cardiovascular implants - Endovascular devices - Part 1: Endovascular prostheses

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Organization: BSI
Publication Date: 27 March 2003
Status: inactive
Page Count: 96
ICS Code (Implants for surgery, prosthetics and orthotics): 11.040.40

Document History

BS EN ISO 25539-1
March 31, 2017
Cardiovascular implants — Endovascular devices Part 1: Endovascular prostheses
A description is not available for this item.
BS EN ISO 25539-1
March 31, 2017
Cardiovascular implants — Endovascular devices Part 1: Endovascular prostheses
A description is not available for this item.
BS ISO 25539-1
March 27, 2003
Cardiovascular implants - Endovascular devices - Part 1: Endovascular prostheses
This part of ISO 25539 specifies requirements for endovascular prostheses, based upon current medical knowledge. With regard to safety, it gives requirements for intended performance, design...
BS EN ISO 25539-1
March 27, 2003
Cardiovascular implants - Endovascular devices - Part 1: Endovascular prostheses
A description is not available for this item.
BS EN ISO 25539-1
March 27, 2003
Cardiovascular implants - Endovascular devices - Part 1: Endovascular prostheses
This part of ISO 25539 specifies requirements for endovascular prostheses, based upon current medical knowledge. With regard to safety, it gives requirements for intended performance, design...
BS EN ISO 25539-1
March 27, 2003
Cardiovascular implants - Endovascular devices - Part 1: Endovascular prostheses
A description is not available for this item.
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References

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 references:
AAMI ST67 - Sterilization of health care products—Requirements and guidance for selecting a sterility assurance level (SAL) for products labeled “sterile”
Published by AAMI on January 1, 2019
Inclusions This standard specifies requirements and provides guidance on selecting approaches to establish assurance of sterility for a health care product labelled as “sterile.” Approaches to...
This document is referenced by:
BS BIP 0113 - A Guide to European Medical Device Trials and BS EN ISO 14155
Published by BSI on June 13, 2012
A description is not available for this item.

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