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SRPS EN ISO 10993-10:2014

Biological evaluation of medical devices - Part 10: Tests for irritation and skin sensitization (ISO 10993-10:2010)

Jul 31, 2014
95.99   Withdrawal of Standard   Mar 30, 2023

General information

95.99     Mar 30, 2023

ISS

Z076

European Norm

11.100.20  

English  

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Scope

ISO 10993-10:2010 describes the procedure for the assessment of medical devices and their constituent materials with regard to their potential to produce irritation and skin sensitization.
ISO 10993-10:2010 includes:

pretest considerations for irritation, including in silico and in vitro methods for dermal exposure;
details of in vivo (irritation and sensitization) test procedures;
key factors for the interpretation of the results.

Instructions are given for the preparation of materials specifically in relation to the above tests and several special irritation tests are described for application of medical devices in areas other than skin.

Related directives

NOTE: If the word "harmonized" (marked in green) is not found in the field with the name of the directive, it means that the European standard is not cited in the OJEU.

93/42/EEC

Medical devices

Life cycle

PREVIOUSLY

WITHDRAWN
SRPS EN ISO 10993-10:2011

NOW

WITHDRAWN
SRPS EN ISO 10993-10:2014
95.99 Withdrawal of Standard
Mar 30, 2023

REVISED BY

PUBLISHED
SRPS EN ISO 10993-10:2023

Related project

Adopted from EN ISO 10993-10:2013

Adopted from ISO 10993-10:2010 IDENTICAL