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ISO 14971 FRENCH

Dispositifs médicaux - Application de la gestion des risques aux dispositifs médicaux

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Organization: ISO
Publication Date: 1 March 2007
Status: inactive
Page Count: 96
ICS Code (Medical equipment in general): 11.040.01

Document History

ISO 14971 FRENCH
December 1, 2019
Dispositifs médicaux — Application de la gestion des risques aux dispositifs médicaux
A description is not available for this item.
ISO 14971 FRENCH
March 1, 2007
Dispositifs médicaux - Application de la gestion des risques aux dispositifs médicaux
A description is not available for this item.

References

This document references:
IEC 60601-1-6 - Medical electrical equipment – Part 1-6: General requirements for basic safety and essential performance – Collateral standard: Usability
Published by IEC on July 1, 2020
This International Standard specifies a PROCESS for a MANUFACTURER to analyse, specify, develop and evaluate the USABILITY, as it relates to BASIC SAFETY and ESSENTIAL PERFORMANCE of MEDICAL...
This document references:
IEC 60601-1-8 - Medical electrical equipment – Part 1-8: General requirements for basic safety and essential performance – Collateral standard: General requirements, tests and guidance for alarm systems in medical electrical equipment and medical electrical systems
Published by IEC on July 1, 2020
This International Standard applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of MEDICAL ELECTRICAL EQUIPMENT and MEDICAL ELECTRICAL SYSTEMS, hereafter referred to as ME EQUIPMENT and ME SYSTEMS....
This document is referenced by:
ISO 7439 - Copper-bearing contraceptive intrauterine devices - Requirements and tests
Published by ISO on February 15, 2015
This International Standard specifies requirements and tests for single-use, copper-bearing contraceptive intrauterine devices (IUDs) and their insertion instruments. It is not applicable to IUDs...
This document is referenced by:
BS EN ISO 13485 + A11 - Medical devices - Quality management systems - Requirements for regulatory purposes
Published by BSI on March 31, 2016
A description is not available for this item.
This document is referenced by:
BS EN 14180 - Sterilizers for medical purposes — Low temperature steam and formaldehyde sterilizers — Requirements and testing
Published by BSI on May 31, 2014
A description is not available for this item.
This document is referenced by:
ISO 13022 - Medical products containing viable human cells - Application of risk management and requirements for processing practices
Published by ISO on April 1, 2012
This International Standard specifies requirements and guidance for processing practices and managing risk associated with viable cellular components of products regulated as medicinal products,...
This document is referenced by:
ISO 8600-1 - Endoscopes - Medical endoscopes and endotherapy devices - Part 1: General requirements
Published by ISO on October 15, 2015
This part of ISO 8600 gives definitions of terms and requirements for endoscopes and endotherapy devices used in the practice of medicine.
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