99.60 Withdrawal effective Jun 3, 2020
CEN
CEN/TC 205 Non-active medical devices
European Norm
11.040.20 Transfusion, infusion and injection equipment
Withdrawn
ISO 8871-2:2003 specifies evaluation procedures applicable to elastomeric parts used for drug containers and medical devices in order to guarantee the product identity between the samples evaluated in the (suitability test) acceptance process and the current supplies. The physical and chemical test procedures specified in this part of ISO 8871 permit the determination of the typical characteristics of rubber materials, and may serve as a basis for agreements between manufacturer and user regarding the product consistency in subsequent supplies. An appropriate set of tests is selected, depending upon the type of rubber and its application.
This part of ISO 8871 does not specify other requirements for rubber materials. These are laid down in the relevant product standards.
WITHDRAWN
EN ISO 8871-2:2004
99.60
Withdrawal effective
Jun 3, 2020
WITHDRAWN
EN ISO 8871-2:2004/A1:2014
PUBLISHED
EN ISO 8871-2:2020