I.S. EN ISO 25424:2019
Current
The latest, up-to-date edition.
Sterilization of health care products - Low temperature steam and formaldehyde - Requirements for development, validation and routine control of a sterilization process for medical devices (ISO 25424:2018)
Hardcopy , PDF
English
12-08-2019
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Foreword
Introduction
1 Scope
2 Normative references
3 Terms and definitions
4 Quality management system elements
5 Sterilizing agent characterization
6 Process and equipment characterization
7 Product definition
8 Process definition
9 Validation
10 Routine monitoring and control
11 Product release from sterilization
12 Maintaining process effectiveness
Annex A (normative) Process definition based on inactivation of reference microorganisms and knowledge of bioburden on product items to be sterilized
Annex B (normative) Process definition based on inactivation of reference microorganisms
Annex C (informative) Guidance on application of this document
Annex D (informative) Environmental aspects regarding development, validation and routine control of low temperature steam and formaldehyde processes
Bibliography
This document specifies requirements for the development, validation and routine control of a low temperature steam and formaldehyde (LTSF) sterilization process for medical devices using a mixture of low temperature steam and formaldehyde as sterilizing agent and which operates below ambient pressure.
| Committee |
TC 198
|
| DocumentType |
Standard
|
| Pages |
0
|
| ProductNote |
NOTE: The date of any NSAI previous adoption may not match the date of its original CEN/CENELEC document. THIS STANDARD ALSO REFERS TO EN 556-1
|
| PublisherName |
National Standards Authority of Ireland
|
| Status |
Current
|
| Supersedes |
| Standards | Relationship |
| EN ISO 25424:2019 | Identical |
| ISO 25424:2018 | Identical |
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