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Standard [WITHDRAWN]
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This document (EN ISO 8871-2:2004 + A1:2014) includes the German version of Amendment 1 (ISO 8871-2:2003/Amd1:2005) that has been taken over as EN ISO 8871-2:2004/A1:2014 by CEN/TC 205 "Non-active medical devices". DIN EN ISO 8871-2 specifies procedures applicable to elastomeric parts used for drug containers and medical devices in order to ensure the product identity between the samples evaluated in the (suitability test) acceptance process and the current supplies. The physical and chemical test procedures included in this standard 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. With Amendment 1, an informative Annex on a method for the determination of a fingerprint by surface infrared spectroscopy has been added.
This document replaces DIN EN ISO 8871-2:2004-11 .
This document has been replaced by: DIN EN ISO 8871-2:2020-09 .