BS EN ISO 11138-1:2017 Sterilization of health care products. Biological indicators. General requirements

BS EN ISO 11138-1:2017

Sterilization of health care products. Biological indicators. General requirements

Status : Current   Published : April 2017

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PDF

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HARDCOPY



What is this standard about?

 This is the first part of a five part standard (the ISO 11138 series) on the sterilization of health care products and biological indicators. The series represents the current “state-of-the-art” according to the expert manufacturers, users and regulatory authorities involved in developing this document. 

This standard covers: general and specific manufacturing requirements, determination of population and resistance, and culture conditions. 

The other parts of the standard are:

Who is this standard for?

  • Sterilization equipment manufacturers
  • Sterilization service providers
  • Infection control professionals
  • Other professionals responsible for sterilization

Why should you use this standard?

It specifies 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.

It also specifies basic and common requirements that are applicable to all parts of ISO 11138. Requirements for biological indicators for particular specified processes are provided in the relevant parts of ISO 11138. If no specific subsequent part is provided, this document applies. 

NOTE 1: National or regional regulations can apply.

NOTE 2: This document does not apply to microbiological test systems for processes that rely on physical removal of microorganisms, e.g. filtration processes or processes that combine physical and/or mechanical removal with microbiological inactivation, such as use of washer disinfectors or flushing and steaming of pipelines. This document, however, can contain elements relevant to such microbiological test systems.

What’s changed since the last update?

This standard is a full technical revision of the 2006 version, which makes the following amendments:

  • Normative references and bibliography updated
  • Terms and definitions “FBIO-value” and “packaging system” deleted
  • General manufacturing requirements (clause 4) including Table 1 revised, e.g. requirements on traceability added
  • Requirements on carrier and the primary and secondary packaging revised General resistance requirements (6.1.2 and 6.4.3) revised
  • Requirements on software validation (7.4) and detection systems (7.5) added
  • For determination of growth inhibition by carriers and primary packaging materials exposed to sterilization processes the number of probes was increased and requirements revised (see Annex B)



Standard NumberBS EN ISO 11138-1:2017
TitleSterilization of health care products. Biological indicators. General requirements
StatusCurrent
Publication Date30 April 2017
Normative References(Required to achieve compliance to this standard)ISO 18472:2018, ISO 17665-1, BS EN ISO 18472:2018, ISO 14937, ISO 11135, ISO 11737-1:2006
Informative References(Provided for Information)ISO 11140-1, ISO/TS 11139:2006, ISO 80000, ISO 15223-1, IEC 60027, ISO 13485, ISO 8601, ISO 14161:2009
ReplacesBS EN ISO 11138-1:2006
International RelationshipsEN ISO 11138-1:2017,ISO 11138-1:2017
Draft Superseded By15/30321502 DC
DescriptorsPerformance testing, Sterilization (hygiene), Bioassay, Microorganisms, Sterilizers, Medical equipment, Biological analysis and testing, Microbiological analysis, Culture techniques, Culture containers, Packaging, Labelling (process)
ICS11.080.01
11.080.20
Title in FrenchStérilisation des produits de santé. Indicateurs biologiques. Exigences générales
Title in GermanSterilisation von Produkten für die Gesundheitsfürsorge. Biologische Indikatoren. Allgemeine Anforderungen
CommitteeCH/198
ISBN978 0 580 89831 0
PublisherBSI
FormatA4
DeliveryYes
Pages52
File Size2.438 MB
Price£254.00


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