UNLIMITED FREE
ACCESS TO THE WORLD'S BEST IDEAS

SUBMIT
Already a GlobalSpec user? Log in.

This is embarrasing...

An error occurred while processing the form. Please try again in a few minutes.

Customize Your GlobalSpec Experience

Select Your Free Newsletters

Industry Newsletters

Select Your Free Product Alerts

Finish!
Privacy Policy

This is embarrasing...

An error occurred while processing the form. Please try again in a few minutes.

BSI - 22/30409835 DC

Draft BS EN ISO 17665 Sterilization of health care products - Moist heat - Requirements for the development, validation and routine control of a sterilization process for medical devices

pending, Most Current
Organization: BSI
Publication Date: 6 September 2022
Status: pending
Page Count: 161
ICS Code (Sterilization and disinfection in general): 11.080.01

Document History

22/30409835 DC
September 6, 2022
Draft BS EN ISO 17665 Sterilization of health care products - Moist heat - Requirements for the development, validation and routine control of a sterilization process for medical devices
A description is not available for this item.

References

This document references:
TIR17 - Compatibility of materials subject to sterilization
Published by AAMI on January 1, 2017
This document provides guidance for health care product manufacturers in the selection and qualification of polymeric materials, ceramics, and metals for use in health care products sterilized by the...
This document references:
EN 12442-1 - Animal Tissues and Their Derivatives Utilized in the Manufacture of Medical Devices - Part 1: Analysis and Management of Risk
Published by CEN on September 1, 2000
A description is not available for this item.
This document references:
EN 12442-2 - Animal Tissues and Their Derivatives Utilized in the Manufacture of Medical Devices - Part 2: Controls on Sourcing, Collection and Handling
Published by CEN on September 1, 2000
A description is not available for this item.
This document references:
EN 12442-3 - Animal Tissues and Their Derivatives Utilized in the Manufacture of Medical Devices - Part 3: Validation of the Elimination and/or Inactivation of Viruses and Transmissible Agents
Published by CEN on September 1, 2000
A description is not available for this item.
This document references:
EN 13060 - Small steam sterilizers
Published by CEN on December 1, 2014
This European Standard specifies the performance requirements and test methods for small steam sterilizers and sterilization cycles which are used for medical purposes or for materials that are...
View Less
View All
Advertisement