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 10993-17

Biological evaluation of medical devices Part 17: Toxicological risk assessment of medical device constituents

active, Most Current
Organization: BSI
Publication Date: 30 November 2023
Status: active
Page Count: 80
ICS Code (Biological evaluation of medical devices): 11.100.20

Document History

BS EN ISO 10993-17
November 30, 2023
Biological evaluation of medical devices Part 17: Toxicological risk assessment of medical device constituents
A description is not available for this item.
BS EN ISO 10993-17
June 30, 2009
Biological evaluation of medical devices Part 17: Establishment of allowable limits for leachable substances
A description is not available for this item.
BS EN ISO 10993-17
April 30, 2003
Biological evaluation of medical devices - Part 17: Establishment of allowable limits for leachable substances
A description is not available for this item.

References

This document references:
ISO TS 21726 - Biological evaluation of medical devices - Application of the threshold of toxicological concern (TTC) for assessing biocompatibility of medical device constituents
Published by ISO on February 1, 2019
This document describes the basis for, selection of, and general applicability of a threshold of toxicological concern (TTC) value for a constituent present in/on a medical device or released from a...
This document is referenced by:
BS PD ISO/TR 15499 - TC - Tracked Changes (Redline) - Biological evaluation of medical devices - Guidance on the conduct of biological evaluation within a risk management process
Published by BSI on February 26, 2020
A description is not available for this item.
This document is referenced by:
BS EN ISO 14971 + A11 - Medical devices - Application of risk management to medical devices
Published by BSI on December 31, 2019
A description is not available for this item.
This document is referenced by:
BS EN ISO 14160 - Sterilization of health care products - Liquid chemical sterilizing agents for single-use medical devices utilizing animal tissues and their derivatives - Requirements for characterization, development, validation and routine control of a sterilization process for medical devices
Published by BSI on July 31, 2011
A description is not available for this item.
View Less
View All
Advertisement