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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 December 2019
Status: active
Page Count: 48
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:
ISO 18153 - In vitro diagnostic medical devices - Measurement of quantities in biological samples - Metrological traceability of values for catalytic concentration of enzymes assigned to calibrators and control materials
Published by ISO on August 15, 2003
A description is not available for this item.
This document references:
ISO 19001 - In vitro diagnostic medical devices - Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biology
Published by ISO on March 15, 2013
This International Standard specifies requirements for information supplied by the manufacturer with reagents used in staining in biology. It applies to producers, suppliers and vendors of dyes,...
This document references:
ISO 10993-2 - Biological evaluation of medical devices Part 2: Animal welfare requirements
Published by ISO on July 15, 2006
This part of ISO 10993 is aimed at those who commission, design and perform tests or evaluate data from animal tests undertaken to assess the biocompatibility of materials intended for use in medical...
This document is referenced by:
ASTM F2503 - Standard Practice for Marking Medical Devices and Other Items for Safety in the Magnetic Resonance Environment
Published by ASTM on February 1, 2020
This international standard applies to the practice of marking of items that might be used in the magnetic resonance (MR) environment. The purpose of this practice is to mark items that might be...
This document is referenced by:
AAMI TIR69 - Risk management of radio-frequency wireless coexistence for medical devices and systems
Published by AAMI on January 1, 2017
This TIR applies to medical devices and systems (also known as medical electrical equipment) that incorporate RF wireless technology used to perform or control a medical function or to communicate...
This document is referenced by:
ISO 9626 - Stainless steel needle tubing for the manufacture of medical devices - Requirements and test methods
Published by ISO on August 1, 2016
This International Standard applies to rigid stainless steel needle tubing suitable for use in the manufacture of hypodermic needles and other medical devices primarily for human use. This...
This document is referenced by:
QUALITY SYSTEM COMPENDIUM - The Quality System Compendium CGMP Requiremements and Industry Practice
Published by AAMI on January 1, 2019
A description is not available for this item.
This document is referenced by:
NEN-EN-ISO/IEEE 11073-20601 - Health informatics - Device interoperability - Part 20601: Personal health device communication - Application profile - Optimized exchange protocol
Published by NEN on February 1, 2023
Within the context of the ISO/IEEE 11073 personal health device standard family, this standard defines an optimized exchange protocol and modeling techniques to be used by implementers of personal...
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