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I.S. EN ISO 11135:2014&A1:2019/LC:2019

Current

Current

Sterilization of health-care products - Ethylene oxide - Requirements for the development, validation and routine control of a sterilization process for medical devices - Amendment 1: Revision of Annex E, Single batch release (ISO 11135:2014/Amd 1:2018)

Available format(s)

Hardcopy , PDF

Language(s)

English

Published date

12-11-2019

US$144.33
Excluding Tax where applicable
Summarise this standard

For Harmonized Standards, check the EU site to confirm that the Standard is cited in the Official Journal.

Only cited Standards give presumption of conformance to New Approach Directives/Regulations.

Foreword
Introduction
1 Scope
2 Normative references
3 Terms and definitions
4 Quality management systems
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) Determination of lethal rate of the sterilization process — Biological indicator/bioburden approach
Annex B (normative) Conservative determination of lethal rate of the sterilization process — Overkill approach
Annex C (informative) Temperature sensors, RH sensors and biological indicator numbers
Annex D (informative) Guidance on the application of the normative requirements
Annex E (normative) Single Lot Release
Bibliography

This International Standard specifies requirements for the development, validation and routine control of an ethylene oxide sterilization process for medical devices in both the industrial and health care facility settings, and it acknowledges the similarities and differences between the two applications.

Committee
ISO/TC 198
DocumentType
Standard
Pages
128
ProductNote
THIS STANDARD IS ALSO REFERES TO ISO 11138-2 ISO 13485, AAMI ST41,AS/NZS 4187 The date of any NSAI previous adoption may not match the date of its original CEN/CENELEC document.
PublisherName
National Standards Authority of Ireland
Status
Current
Supersedes

Standards Relationship
ISO 11135:2014/Amd 1:2018 Identical

Frequently Asked Questions

I.S. EN ISO 11135 specifies development, validation and routine control requirements for ethylene oxide sterilisation processes. It is an Irish standard published by National Standards Authority of Ireland (NSAI).

I.S. EN ISO 11135 is used by medical device manufacturers and sterilisation service providers using ethylene oxide. It is an Irish standard published by National Standards Authority of Ireland (NSAI).

I.S. EN ISO 11135 is National Standards Authority of Ireland (NSAI)'s standard for ethylene oxide sterilisation of healthcare products, while I.S. EN ISO 11137-1 covers radiation sterilisation of healthcare products (Ireland). I.S. EN ISO 11135 specifies development, validation and routine control requirements for ethylene oxide sterilisation processes. I.S. EN ISO 11137-1 specifies development, validation, dose establishment or routine control requirements for radiation sterilisation.

No — I.S. EN ISO 11135 is an Irish standard published by National Standards Authority of Ireland (NSAI), with its listed region as Ireland.

I.S. EN ISO 11135 specifies development, validation and routine control requirements for ethylene oxide sterilisation processes. In practice it is applied by medical device manufacturers and sterilisation service providers using ethylene oxide.
US$144.33
Excluding Tax where applicable