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.

BSI - BS EN ISO 22442-1

Medical devices utilizing animal tissues and their derivatives Part 1: Application of risk management

active, Most Current
Buy Now
Organization: BSI
Publication Date: 31 December 2020
Status: active
Page Count: 38
ICS Code (Medical science): 11.020.20

Document History

BS EN ISO 22442-1
December 31, 2020
Medical devices utilizing animal tissues and their derivatives Part 1: Application of risk management
A description is not available for this item.
BS EN ISO 22442-1
November 30, 2015
Medical devices utilizing animal tissues and their derivatives Part 1: Application of risk management
A description is not available for this item.
BS EN ISO 22442-1
February 29, 2008
Medical devices utilizing animal tissues and their derivatives - Part 1: Application of risk management
A description is not available for this item.

References

This document references:
ISO TS 10993-19 - Biological evaluation of medical devices — Part 19: Physico-chemical, morphological and topographical characterization of materials
Published by ISO on March 1, 2020
This document provides a compilation of parameters and test methods that can be useful for the identification and evaluation of the physical, i.e. physico‑chemical, morphological and topographical...
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 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 2206 - Packaging - Complete, Filled Transport Packages - Identification of Parts When Testing
Published by ISO on January 1, 1987
A description is not available for this item.
This document references:
ISO 10993-14 - Biological Evaluation of Medical Devices - Part 14: Identification and Quantification of Degradation Products from Ceramics
Published by ISO on November 15, 2001
This part of ISO 10993 specifies two methods of obtaining solutions of degradation products from ceramics (including glasses) for the purposes of quantification. It also gives guidance on the...
This document is referenced by:
BS EN ISO 14630 - Non-active surgical implants - General requirements
Published by BSI on December 31, 2012
A description is not available for this item.
This document is referenced by:
BS EN ISO 22523 - External limb prostheses and external orthoses - Requirements and test methods
Published by BSI on October 31, 2006
A description is not available for this item.
This document is referenced by:
BS EN ISO 5840-3 - Cardiovascular implants - Cardiac valve prostheses Part 3: Heart valve substitutes implanted by transcatheter techniques
Published by BSI on February 28, 2021
A description is not available for this item.
This document is referenced by:
BS PD ISO/TS 10993-19 - Biological evaluation of medical devices Part 19: Physico-chemical, morphological and topographical characterization of materials
Published by BSI on March 31, 2020
A description is not available for this item.
This document is referenced by:
BS EN ISO 20857 - Sterilization of health care products - Dry heat - Requirements for the development, validation and routine control of a sterilization process for medical devices
Published by BSI on April 30, 2013
A description is not available for this item.
View Less
View All
Advertisement