Sterilization of health care products - Chemical indicators - Part 1: General requirements (Adopted ISO 11140-1:2014, third edition, 2014-11-01)
Formats Available:
Online,Print
Receive a printed paperback book
Shipped via Canada Post
Receive a printed binder(s)
Shipped via Canada Post
Receive a printed hardcover book
Shipped via Canada Post
Receive access to an electronic copy viewable in a web browser or the Orderline Reader app (Click here to view a demo)
Orderline Reader app available for Windows, Mac, Android, and iOS (Click here to download)
Offline access via Orderline Reader app
Reflowable layout suitable for viewing on any device Orderline Reader app
Font-size controls
Text to speech
Built-in search feature
Google and Wikipedia lookup
Ability to add custom highlights, bookmarks, and notes
Can be registered on up to 3 personal devices total (example: computer, laptop, phone)
Receive access to an online PDF copy viewable in a web browser
Offline access via bookmark to a cached web page
Single user access on up to 3 devices
All online copies are watermarked with your license information
Receive access to an online course viewable in a web browser
Receive access to an online course viewable in a web browser
Receive access to an interactive online copy viewable in a web browser (Click here to view a demo)
Searchable
Printable
Expandable images
Drop-down definitions
Links
Receive access to an online webinar hosted through Zoom
Product Overview
CAN/CSA-ISO 11140-1:16
CSA Group
Sterilization of health care products - Chemical indicators - Part 1: General requirements (Adopted ISO 11140-1:2014, third edition, 2014-11-01)
Total
As low as$165.00
More About This Product
Description
Preface This is the third edition of CAN/CSA-ISO 11140-1, Sterilization of health care products — Chemical indicators — Part 1: General requirements, which is an adoption without modification of the identically titled ISO (International Organization for Standardization) Standard 11140-1 (third edition, 2014-11-01). It supersedes the previous edition published in 2007 as CAN/CSA-Z11140-1 (adopted ISO 11140-1:2005). For brevity, this Standard will be referred to as "CAN/CSA-ISO 11140-1" throughout. Scope This part of ISO 11140 specifies general requirements and test methods for indicators that show exposure to sterilization processes by means of physical and/or chemical change of substances, and which are used to monitor the attainment of one or more of the process parameter (s) specified for a sterilization process. They are not dependent for their action on the presence or absence of a living organism. NOTE 1 : Biological test systems are regarded as those test systems which are dependent for their interpretation on the demonstration of the viability of an organism. Test systems of this type are considered in the ISO 11138-series for biological indicators (BIs). The requirements and test methods of this part of ISO 11140 apply to all indicators specified in subsequent parts of ISO 11140, unless the requirement is modified or added to by a subsequent part, in which case the requirement of that particular part will apply. Relevant test equipment is described in ISO 18472. NOTE 2 : Additional requirements for specific test indicators/indicator systems (Type 2 indicators) are given in ISO 11140-3, ISO 11140-4 and ISO 11140-5.
Preface This is the third edition of CAN/CSA-ISO 11140-1, Sterilization of health care products — Chemical indicators — Part 1: General requirements, which is an adoption without modification of the identically titled ISO (International Organization for Standardization) Standard 11140-1 (third edition, 2014-11-01). It supersedes the previous edition published in 2007 as CAN/CSA-Z11140-1 (adopted ISO 11140-1:2005). For brevity, this Standard will be referred to as "CAN/CSA-ISO 11140-1" throughout. Scope This part of ISO 11140 specifies general requirements and test methods for indicators that show exposure to sterilization processes by means of physical and/or chemical change of substances, and which are used to monitor the attainment of one or more of the process parameter (s) specified for a sterilization process. They are not dependent for their action on the presence or absence of a living organism. NOTE 1 : Biological test systems are regarded as those test systems which are dependent for their interpretation on the demonstration of the viability of an organism. Test systems of this type are considered in the ISO 11138-series for biological indicators (BIs). The requirements and test methods of this part of ISO 11140 apply to all indicators specified in subsequent parts of ISO 11140, unless the requirement is modified or added to by a subsequent part, in which case the requirement of that particular part will apply. Relevant test equipment is described in ISO 18472. NOTE 2 : Additional requirements for specific test indicators/indicator systems (Type 2 indicators) are given in ISO 11140-3, ISO 11140-4 and ISO 11140-5.