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PD ISO/TR 13154:2017

Current
Current

The latest, up-to-date edition.

Medical electrical equipment. Deployment, implementation and operational guidelines for identifying febrile humans using a screening thermograph
Available format(s)

Hardcopy , PDF

Language(s)

English

Published date

03-31-2017

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
Alphabetical index

Gives general guidelines for the deployment, implementation and operation of a SCREENING THERMOGRAPH intended to be used for non-invasive febrile temperature screening of individuals under indoor environmental conditions to prevent the spread of infection.

This document provides general guidelines for the deployment, implementation and operation of a screening thermograph intended to be used for non-invasive febrile temperature screening of individuals under indoor environmental conditions to prevent the spread of infection. NOTE The equipment standard for screening thermographs is found in IEC80601–2-59.

Committee
CH/121/9
DocumentType
Standard
Pages
36
PublisherName
British Standards Institution
Status
Current
Supersedes

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
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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