Standard

SN EN ISO 17664:2018

Apr 2018 Withdrawn

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Abstract

ISO 17664:2017 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 and/or sterilization to ensure that the device is safe and effective for its intended use. This includes information for processing prior to use or reuse of the medical device. The provisions of ISO 17664:2017 are applicable to medical devices that are intended for invasive or other direct or indirect patient contact.

Products specifications

Standard from INB
Published: April 1 2018
Withdrawn: October 1 2021
Effective: April 1 2018
Document type: EN
Pages
ISBN:

ICS: 11.080.01
Publisher: SNV
Distributor: SNV
National Committee: INB/NK 171
European TC: CEN/TC 204
International TC: ISO/TC 198

Legal references

Swiss Federal Authority: SWISSMEDIC

Designated under following Swiss law:

Law reference	Restrictions
812.213

Designated under following EU law:

Law reference	Restrictions
Council Directive 93/42/EEC

Product Relations

Replaced by: SN EN ISO 17664-1:2021
Adopted from: ISO 17664:2017 , IDT
Replaces: SN EN ISO 17664:2004

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