ISO 10993-4:2017

Biological evaluation of medical devices — Part 4: Selection of tests for interactions with blood

Biological evaluation of medical devices — Part 4: Selection of tests for interactions with blood

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Referenced standards

ASTM F1830-97ASTM F1841-97ASTM F1984-99ASTM F2888-13ASTM F756-13GB/T 16175-2008ISO 10993-10:2010ISO 10993-11:2006ISO 10993-1:2009ISO 10993-2:2006ISO 10993-3:2014ISO 10993-4:2002ISO 10993-5:2009ISO 10993-6:2016ISO 10993-7:2008ISO 10993-9:2009ISO 3826-3:2006ISO 5840-1:2015ISO 5840-2:2015ISO 5840-3:2013ISO 5841-3:2013ISO 7198:2016ISO 7199:2016ISO 8637:2010
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ISO 10993-4:2017

Biological evaluation of medical devices — Part 4: Selection of tests for interactions with blood

Biological evaluation of medical devices — Part 4: Selection of tests for interactions with blood

ISO 10993-4:2017 specifies general requirements for evaluating the interactions of medical devices with blood.

It describes

a) a classification of medical devices that are intended for use in contact with blood, based on the intended use and duration of contact as defined in ISO 10993-1,

b) the fundamental principles governing the evaluation of the interaction of devices with blood,

c) the rationale for structured selection of tests according to specific categories, together with the principles and scientific basis of these tests.

Detailed requirements for testing cannot be specified because of limitations in the knowledge and precision of tests for evaluating interactions of devices with blood. This document describes biological evaluation in general terms and may not necessarily provide sufficient guidance for test methods for a specific device.

The changes in this document do not indicate that testing conducted according to prior versions of this document is invalid. For marketed devices with a history of safe clinical use, additional testing according to this revision is not recommended.

Edition2017
Standard Part No4
Published Date2017
Published ByInternational Standardization Organisation
Page Count69