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EVS-EN 62366-1:2015+A1:2020

Meditsiiniseadmed. Osa 1: Kasutatavusprojekteerimise rakendamine meditsiiniseadmetele

Üldinfo
Kehtiv alates 17.08.2020
Alusdokumendid
EN 62366-1:2015; IEC 62366-1:2015; EN 62366-1:2015/AC:2015; IEC 62366-1:2015/COR1:2016; EN 62366-1:2015/AC:2016-09; IEC 62366-1:2015/A1:2020; EN 62366-1:2015/A1:2020
Tegevusala (ICS grupid)
11.040 Meditsiinivarustus
Direktiivid või määrused
puuduvad
Standardi ajalugu
Staatus
Kuupäev
Tüüp
Nimetus
17.08.2020
Põhitekst + muudatus
17.08.2020
Muudatus
01.08.2018
Parandus
05.01.2016
Parandus
07.05.2015
Põhitekst
This part of IEC 62366 specifies a PROCESS for a MANUFACTURER to analyse, specify, develop and evaluate the USABILITY of a MEDICAL DEVICE as it relates to SAFETY. This USABILITY ENGINEERING (HUMAN FACTORS ENGINEERING) PROCESS permits the MANUFACTURER to assess and mitigate RISKS associated with NORMAL USE, i.e., CORRECT USE and USE ERROR. It can be used to identify but does not assess or mitigate RISKS associated with ABNORMAL USE. NOTE 1 Safety is freedom from unacceptable risk. Unacceptable risk can arise from use error, which can lead to exposure to hazards including loss or degradation of clinical performance. NOTE 2 Guidance on the application of USABILITY ENGINEERING to MEDICAL DEVICES is available in IEC 62366-22, which addresses not only SAFETY but also aspects of USABILITY not related to SAFETY. If the USABILITY ENGINEERING PROCESS detailed in this International Standard has been complied with, then the USABILITY of a MEDICAL DEVICE as it relates to SAFETY is presumed to be acceptable, unless there is OBJECTIVE EVIDENCE to the contrary. NOTE 3 Such OBJECTIVE EVIDENCE can subsequently originate from POST-PRODUCTION surveillance.
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Standardi monitooring
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CEN ISO/TR 24971:2020

Medical devices - Guidance on the application of ISO 14971 (ISO/TR 24971:2020)
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Uusim versioon Kehtiv alates 02.03.2016
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EVS-EN 62304:2006+A1:2015

Meditsiiniseadmete tarkvara. Tarkvara elutsükli protsessid
Uusim versioon Kehtiv alates 15.11.2019