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SRPS EN ISO 25424:2012

Sterilization of medical devices - Low temperature steam and formaldehyde - Requirements for development, validation and routine control of a sterilization process for medical devices (ISO 25424:2009)

Jun 21, 2012
95.99   Withdrawal of Standard   May 29, 2020

General information

95.99     May 29, 2020

ISS

Z076

European Norm

11.080.01  

English  

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Scope

ISO 25424:2009 specifies requirements for the development, validation and routine control of a Low Temperature Steam and Formaldehyde (LTSF) sterilization process for medical devices.
ISO 25424:2009 is intended to be applied by process developers, manufacturers of sterilization equipment, manufacturers of medical devices to be sterilized and the organizations with responsibility for sterilizing medical devices.
ISO 25424:2009 covers sterilization processes that use a mixture of low temperature steam and formaldehyde as sterilant, and which are working below ambient pressure only.

Related directives

NOTE: If the word "harmonized" (marked in green) is not found in the field with the name of the directive, it means that the European standard is not cited in the OJEU.

93/42/EEC

Medical devices

Life cycle

NOW

WITHDRAWN
SRPS EN ISO 25424:2012
95.99 Withdrawal of Standard
May 29, 2020

REVISED BY

PUBLISHED
SRPS EN ISO 25424:2020

Related project

Adopted from EN ISO 25424:2011

Adopted from ISO 25424:2009 IDENTICAL