BS EN ISO 11138-5:2017
Current
The latest, up-to-date edition.
Sterilization of health care products. Biological indicators Biological indicators for low-temperature steam and formaldehyde sterilization processes
Hardcopy , PDF
English
30-04-2017
Committee |
CH/198
|
DevelopmentNote |
Supersedes BS EN 866-5 and 04/30078111 DC (08/2006) Supersedes 15/30321514 DC. (04/2017)
|
DocumentType |
Standard
|
Pages |
18
|
PublisherName |
British Standards Institution
|
Status |
Current
|
Supersedes |
This document specifies requirements for test organisms, suspensions, inoculated carriers, biological indicators and test methods intended for use in assessing the performance of sterilization processes employing low-temperature steam and formaldehyde as the sterilizing agent.
NOTE1 Requirements for validation and control of low-temperature steam and formaldehyde sterilization processes are provided by ISO14937 .
NOTE2 Requirements for work place safety can be provided by national or regional regulations.
Standards | Relationship |
EN ISO 11138-5:2017 | Identical |
I.S. EN ISO 11138-5:2017 | Identical |
NEN EN ISO 11138-5 : 2017 | Identical |
UNI EN ISO 11138-5 : 2006 | Identical |
NS EN ISO 11138-5 : 2017 | Identical |
SN EN ISO 11138-5 : 2017 | Identical |
DIN EN ISO 11138-5:2015-10 (Draft) | Identical |
NBN EN ISO 11138-5 : 2006 | Identical |
ISO 11138-5:2017 | Identical |
UNE-EN ISO 11138-5:2017 | Identical |
NF EN ISO 11138-5 : 2017 | Identical |
ISO 14937:2009 | Sterilization of health care products General requirements for characterization of a sterilizing agent and the development, validation and routine control of a sterilization process for medical devices |
ISO 25424:2009 | Sterilization of medical devices Low temperature steam and formaldehyde Requirements for development, validation and routine control of a sterilization process for medical devices |
EN 14180:2014 | Sterilizers for medical purposes - Low temperature steam and formaldehyde sterilizers - Requirements and testing |
ISO 11138-1:2017 | Sterilization of health care products — Biological indicators — Part 1: General requirements |
ISO 14161:2009 | Sterilization of health care products Biological indicators Guidance for the selection, use and interpretation of results |
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