CSA ISO TR 13154 : 2014
Withdrawn
A Withdrawn Standard is one, which is removed from sale, and its unique number can no longer be used. The Standard can be withdrawn and not replaced, or it can be withdrawn and replaced by a Standard with a different number.
View Superseded by
MEDICAL ELECTRICAL EQUIPMENT - DEPLOYMENT, IMPLEMENTATION AND OPERATIONAL GUIDELINES FOR IDENTIFYING FEBRILE HUMANS USING A SCREENING THERMOGRAPH
Hardcopy , PDF
30-07-2021
English
01-01-2014
Foreword
Introduction
1 Scope
2 Normative references
3 Terms and definitions
4 General considerations
5 Planning for deployment
6 Operation
7 Data storage and security
Annex A (informative) - Deployment considerations
Annex B (informative) - Example facial thermograms
Bibliography
Specifies general guidelines for the deployment, implementation and operation of a screening thermograph intended to be used for individual non-invasive febrile temperature screening of humans under indoor environmental conditions to prevent the spread of infection.
DocumentType |
Standard
|
Pages |
36
|
PublisherName |
Canadian Standards Association
|
Status |
Withdrawn
|
SupersededBy |
Standards | Relationship |
ISO/TR 13154:2017 | Identical |
IEC 60601-1:2005+AMD1:2012 CSV | Medical electrical equipment - Part 1: General requirements for basic safety and essential performance |
ISO 80601-2-56:2017 | Medical electrical equipment — Part 2-56: Particular requirements for basic safety and essential performance of clinical thermometers for body temperature measurement |
IEC 60601-1-6:2010+AMD1:2013 CSV | Medical electrical equipment - Part 1-6: General requirements for basic safety and essential performance - Collateral standard: Usability |
ISO 13485:2016 | Medical devices Quality management systems Requirements for regulatory purposes |
IEC 80601-2-59:2017 | Medical electrical equipment - Part 2-59: Particular requirements for the basic safety and essential performance of screening thermographs for human febrile temperature screening |
ISO 14971:2007 | Medical devices Application of risk management to medical devices |
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