NF EN ISO 11138-1 : 2017
Current
Current
The latest, up-to-date edition.
STERILIZATION OF HEALTH CARE PRODUCTS - BIOLOGICAL INDICATORS - PART 1: GENERAL REQUIREMENTS
Published date
01-12-2013
Publisher
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Describes general requirements for production, labelling, test methods and performance characteristics of biological indicators, including inoculated carriers and suspensions, and their components, to be used in the validation and routine monitoring of sterilization processes.
| DevelopmentNote |
Indice de classement: S98-004-1. PR NF EN ISO 11138-1 October 2004. (10/2004) Supersedes NF EN 866-1 (09/2006)
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| DocumentType |
Standard
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| PublisherName |
Association Francaise de Normalisation
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| Status |
Current
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| Standards | Relationship |
| UNI EN ISO 11138-1 : 2006 | Identical |
| SN EN ISO 11138-1:2017 | Identical |
| UNE-EN ISO 11138-1:2017 | Identical |
| BS EN ISO 11138-1:2017 | Identical |
| EN ISO 11138-1:2017 | Identical |
| I.S. EN ISO 11138-1:2017 | Identical |
| DIN EN ISO 11138-1:2015-10 (Draft) | Identical |
| ISO 11138-1:2017 | Identical |
| NF EN ISO 11135-1 : 2007 | STERILIZATION OF HEALTH CARE PRODUCTS - ETHYLENE OXIDE - PART 1: REQUIREMENTS FOR DEVELOPMENT, VALIDATION AND ROUTINE CONTROL OF A STERILIZATION PROCESS FOR MEDICAL DEVICES |
| NFX 30 503 : 2011 | HEALTHCARE WASTE - REDUCTION OF MICROBIOLOGICAL AND MECHANICAL RISKS FROM POTENTIALLY INFECTIOUS AND OTHER COMPARABLE HEALTHCARE WASTE BY DISINFECTION PRETREATMENT APPLIANCES |
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