We use cookies to enhance your browsing experience, serve personalized content, and analyze our traffic. Cookies are small files of information stored on your device that help us remember your preferences and improve your experience. By clicking ‘Accept All’, you consent to our use of cookies. You are able to reject all non-essential cookies or manage your preferences by . To learn more about our Online Digital and Cookie Notice,
click here.
Cookie Preference Center
Please manage your cookie choices by switching the consent toggles on or off under the Purposes below.
You may change your preference at any time as described in our Cookie Policy
This document is purchased as a PDF (Portable Document Format) and accessed via CSA OnDemand™, where you can view, navigate, and print it, or download it for offline use with Adobe Acrobat Viewer. This PDF contains Digital Rights Management protection and is intended for individual use. Please see Terms of Use for CSA’s copyright license and more information.
1.1 This Standard specifies requirements for portable whole blood glucose monitor systems, as defined in Clause 3.3 of this Standard, hereinafter referred to as blood glucose monitor system(s), used to aid in the determination of an individual's blood glucose concentration for the purpose of diabetes management.
1.1.1 Aspects excluded from scope
This Standard does not address glucose screening and/or monitoring of neonates for hypoglycemia, and glucose testing for individuals with a blood glucose concentration less than 2.5 mmol/L or greater than 19 mmol/L.
Login or Register
View Access for this document is only available for viewers in Canada