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BSI - BS EN ISO 20696

Sterile urethral catheters for single use

active, Most Current
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Organization: BSI
Publication Date: 31 July 2018
Status: active
Page Count: 42
ICS Code (Syringes, needles and catheters): 11.040.25

Document History

BS EN ISO 20696
July 31, 2018
Sterile urethral catheters for single use
A description is not available for this item.
BS EN ISO 20696
July 31, 2018
Sterile urethral catheters for single use
A description is not available for this item.
BS EN ISO 20696
July 31, 2018
Sterile urethral catheters for single use
A description is not available for this item.

References

This document references:
BS EN ISO 80369-1 - Small-bore connectors for liquids and gases in healthcare applications Part 1: General requirements
Published by BSI on November 30, 2018
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:
EN 556-1 - Sterilization of Medical Devices - Requirements for Medical Devices to Be Designated "Sterile" - Part 1: Requirements for Terminally Sterilized Medical Devices
Published by CEN on October 1, 2001
This European Standard specifies the requirements for a terminally-sterilized medical device to be designated "STERILE". Part 2 of this European Standard specifies the requirements for an aseptically...
This document references:
EN 1041 - Information supplied by the manufacturer of medical devices
Published by CEN on August 1, 2008
This European Standard specifies requirements for information to be supplied by a manufacturer for medical devices regulated by Council Directive 90/385/EEC relating to active implantable medical...
This document references:
EN 556-1 - Sterilization of Medical Devices - Requirements for Medical Devices to Be Designated "Sterile" - Part 1: Requirements for Terminally Sterilized Medical Devices
Published by CEN on October 1, 2001
This European Standard specifies the requirements for a terminally-sterilized medical device to be designated "STERILE". Part 2 of this European Standard specifies the requirements for an aseptically...
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