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DIN EN ISO 11135:2014-10

Withdrawn

Withdrawn

A Withdrawn Standard is one, which is removed from sale, and its unique number can no longer be used. The Standard can be withdrawn and not replaced, or it can be withdrawn and replaced by a Standard with a different number.

View Superseded by

STERILIZATION OF HEALTH CARE PRODUCTS - ETHYLENE OXIDE - REQUIREMENTS FOR THE DEVELOPMENT, VALIDATION AND ROUTINE CONTROL OF A STERILIZATION PROCESS FOR MEDICAL DEVICES (ISO 11135:2014)

Available format(s)

Hardcopy , PDF

Language(s)

German, English

Published date

01-10-2014

Withdrawn date

30-01-2021

Superseded by

DIN EN ISO 11135:2020-04

$494.08
Including GST where applicable
Summarise this standard

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
TC 198
DevelopmentNote
Supersedes DIN EN ISO 11135-1 & DIN ISO/TS 11135-2. (10/2014) DRAFT AMD 1 issued in September 2017. (09/2017)
DocumentType
Standard
Pages
92
PublisherName
German Institute for Standardisation (Deutsches Institut für Normung)
Status
Withdrawn
SupersededBy
Supersedes

Standards Relationship
EN ISO 11135:2014 Identical
ISO 11135:2014 Identical
I.S. EN ISO 11135:2014 Equivalent
BS EN ISO 11135:2014 Equivalent

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A newer version of this standard is available.

$494.08
Including GST where applicable