99.60 Withdrawal effective Sep 1, 2002
CEN
CEN/TC 206 Biological and clinical evaluation of medical devices
European Norm
11.040.01 Medical equipment in general | 11.120.01 Pharmaceutics in general
This part of ISO 10993 describes test methods: a) to evaluate the potential of devices and their constituent materials to produce irritation; and b) to evaluate the potential of devices and their constituent materials to produce sensitization. These test methods are recommended for most categories of device and mode of body contact given in ISO 10993-1. Of the tests listed, those appropriate to the end use of the device are to be selected. Guidance is also given for the preparation of materials specifically in relation to the above tests. Note 1: Guidance on the conduct of supplementary tests which may be required specifically for use in the oral, rectal, penile and vaginal areas is given in Annex D.
Legislation related to this standard
WITHDRAWN
EN ISO 10993-10:1995
99.60
Withdrawal effective
Sep 1, 2002
WITHDRAWN
EN ISO 10993-10:2002
