EN ISO 8871-2:2004

Elastomeric parts for parenterals and for devices for pharmaceutical use - Part 2: Identification and characterization (ISO 8871-2:2003) EN ISO 8871-2:2004

Publication date:   Sep 25, 2006

General information

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

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Scope

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.

Life cycle

PREVIOUSLY

WITHDRAWN
EN ISO 8871:1997

WITHDRAWN
EN ISO 8871:1997/A1:1999

NOW

WITHDRAWN
EN ISO 8871-2:2004
99.60 Withdrawal effective
Jun 3, 2020

CORRIGENDA / AMENDMENTS

WITHDRAWN
EN ISO 8871-2:2004/A1:2014

REVISED BY

PUBLISHED
EN ISO 8871-2:2020

Relations

Adopted from ISO 8871-2:2003 IDENTICAL