Customer Support: 131 242

  • Shopping Cart
    There are no items in your cart
We noticed you’re not on the correct regional site. Switch to our AMERICAS site for the best experience.
Dismiss alert
Celebrate World Standards Day. Save 10% with code WSD2026 until 31 Oct. Save now

BS EN ISO 11135:2014

Superseded

Superseded

A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.

Sterilization of health-care products. Ethylene oxide. Requirements for the development, validation and routine control of a sterilization process for medical devices

Available format(s)

Hardcopy , PDF

Language(s)

English

Published date

31-01-2015

Superseded date

16-12-2019

$719.59
Including GST where applicable
Summarise this standard

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
Annex ZA (informative) - Relationship between this
         European Standard and the Essential
         Requirements of EU Directive 90/385/EEC
Annex ZB (informative) - Relationship between this
         European Standard and the Essential
         Requirements of Directive 93/42/EEC

Defines 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
CH/198
DevelopmentNote
Supersedes BS EN ISO 11135-1, DD CEN ISO/TS 11135-2 & 11/30244091 DC. (07/2014)
DocumentType
Standard
Pages
94
PublisherName
British Standards Institution
Status
Superseded
Supersedes

Standards Relationship
ISO 11135:2014 Identical
EN ISO 11135:2014 Identical
DIN EN ISO 11135:2014-10 Equivalent
I.S. EN ISO 11135:2014 Equivalent

$719.59
Including GST where applicable