prEN ISO 10993-4 rev

Biological evaluation of medical devices — Part 4: Selection of tests for interactions with blood prEN ISO 10993-4 rev

General information

10.99 New project approved   Oct 31, 2024

CEN

CEN/TC 206 Biological and clinical evaluation of medical devices

European Norm

Scope

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.

Related legislation

Legislation related to this standard

2017/745

Regulation (EU) 2017/745 of the European Parliament and of the Council of 5 April 2017 on medical devices, amending Directive 2001/83/EC, Regulation (EC) No 178/2002 and Regulation (EC) No 1223/2009 and repealing Council Directives 90/385/EEC and 93/42/EEC

Life cycle

PREVIOUSLY

PUBLISHED
EN ISO 10993-4:2017

IN_DEVELOPMENT
EN ISO 10993-4:2017/prA1

NOW

IN_DEVELOPMENT
prEN ISO 10993-4 rev
10.99 New project approved
Oct 31, 2024