DIN EN ISO 11135:2014-10
Withdrawn
A Withdrawn Standard is one, which is removed from sale, and its unique number can no longer be used. The Standard can be withdrawn and not replaced, or it can be withdrawn and replaced by a Standard with a different number.
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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)
Hardcopy , PDF
German, English
01-10-2014
30-01-2021
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Withdrawn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 |
A newer version of this standard is available.