What is this standard about?
It is a specification stating general requirements for evaluating the interactions of medical devices with blood.
Who is this standard for?
Test laboratories and medical devices manufacturers.
Why should you use this standard?
Because it describes:
What’s changed since the last update?
The 2009 version was updated to match the current tools and techniques used to evaluate medical device blood material interactions. This includes a more current description of in vitro techniques that rely less on the use of animals and generate more predictive results.
EN ISO 10993-4:2017
ISO 10993-4:2017