UNLIMITED FREE
ACCESS TO THE WORLD'S BEST IDEAS

SUBMIT
Already a GlobalSpec user? Log in.

This is embarrasing...

An error occurred while processing the form. Please try again in a few minutes.

Customize Your GlobalSpec Experience

Select Your Free Newsletters

Industry Newsletters

Select Your Free Product Alerts

Finish!
Privacy Policy

This is embarrasing...

An error occurred while processing the form. Please try again in a few minutes.

ISO 22442-1 FRENCH

Dispositifs médicaux utilisant des tissus animaux et leurs dérivés — Partie 1: Application de la gestion des risques

active, Most Current
Buy Now
Organization: ISO
Publication Date: 1 September 2020
Status: active
Page Count: 36
ICS Code (Biological evaluation of medical devices): 11.100.20

Document History

ISO 22442-1 FRENCH
September 1, 2020
Dispositifs médicaux utilisant des tissus animaux et leurs dérivés — Partie 1: Application de la gestion des risques
A description is not available for this item.
ISO 22442-1 FRENCH
November 1, 2015
Dispositifs médicaux utilisant des tissus animaux et leurs dérivés - Partie 1: Application de la gestion des risques
A description is not available for this item.
ISO 22442-1 FRENCH
December 15, 2007
Dispositifs médicaux utilisant des tissus animaux et leurs dérivés - Partie 1: Application de la gestion des risques
A description is not available for this item.

References

This document references:
ISO 10993-1 - Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process
Published by ISO on August 1, 2018
This document specifies: — the general principles governing the biological evaluation of medical devices within a risk management process; — the general categorization of medical devices based on the...
This document references:
ISO TS 10993-20 - Biological evaluation of medical devices Part 20: Principles and methods for immunotoxicology testing of medical devices
Published by ISO on August 1, 2006
This part of ISO 10993 presents an overview of immunotoxicology with particular reference to the potential immunotoxicity of medical devices. It gives guidance on methods for testing for...
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 references:
ISO 13408-2 - Aseptic processing of health care products - Part 2: Sterilizing filtration
Published by ISO on January 1, 2018
This document specifies requirements for sterilizing filtration as part of aseptic processing of health care products conducted in accordance with ISO 13408-1. It also offers guidance to filter users...
This document references:
ISO 10993-3 - Biological evaluation of medical devices - Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity
Published by ISO on October 1, 2014
This part of ISO 10993 specifies strategies for risk estimation, selection of hazard identification tests and risk management, with respect to the possibility of the following potentially...
View Less
View All
Advertisement