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DIN EN ISO 17664

Sterilization of medical devices - Information to be provided by the manufacturer for the processing of resterilizable medical devices (ISO 17664:2004)

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Organization: DIN
Publication Date: 1 July 2004
Status: inactive
Page Count: 23
ICS Code (Sterilization and disinfection in general): 11.080.01

Document History

DIN EN ISO 17664
April 1, 2018
Processing of health care products - Information to be provided by the medical device manufacturer for the processing of medical devices (ISO 17664:2017)
This document specifies requirements for the information to be provided by the medical device manufacturer for the processing of a medical device that requires cleaning followed by disinfection...
DIN EN ISO 17664
June 1, 2016
Processing of health care products - Information to be provided by the medical device manufacturer for the processing of medical devices (ISO/DIS 17664:2016); German and English version prEN ISO 17664:2016
A description is not available for this item.
DIN EN ISO 17664
July 1, 2004
Sterilization of medical devices - Information to be provided by the manufacturer for the processing of resterilizable medical devices (ISO 17664:2004)
A description is not available for this item.

References

This document is referenced by:
DIN EN ISO 11135 - Sterilization of health-care products - Ethylene oxide - Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 11135:2014 + Amd.1:2018) (includes Amendment :2019)
Published by DIN on April 1, 2020
A description is not available for this item.
This document is referenced by:
DIN EN ISO 16635-2 - Dentistry - Dental rubber dam instruments - Part 2: Clamp forceps (ISO 16635-2:2014)
Published by DIN on December 1, 2014
This part of ISO 16635 specifies requirements and test methods for clamp forceps intended for the application of dental rubber dam clamps to teeth.
This document is referenced by:
DIN EN ISO 80601-2-69 - Medical electrical equipment - Part 2-69: Particular requirements for basic safety and essential performance of oxygen concentrator equipment (ISO 80601-2-69:2014)
Published by DIN on December 1, 2014
This particular standard specifies requirements for the BASIC SAFETY and ESSENTIAL PERFORMANCE of an OXYGEN CONCENTRATOR in combination with its ACCESSORIES, hereafter referred to as ME EQUIPMENT,...
This document is referenced by:
DIN EN 13060 - Small steam sterilizers (includes Amendment :2018)
Published by DIN on February 1, 2019
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...
This document is referenced by:
DIN EN 556-2 - Sterilisation von Medizinprodukten - Anforderungen an Medizinprodukte, die als "STERIL" gekennzeichnet werden - Teil 2: Anforderungen an aseptisch hergestellte Medizinprodukte; Deutsche Fassung EN 556-2:2015
Published by DIN on November 1, 2015
Diese Europäische Norm legt die Anforderungen an ein aseptisch hergestelltes Medizinprodukt fest, das als „STERIL“ gekennzeichnet wird. ANMERKUNG Für die Anwendung der EU-Richtlinie(n) für...
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