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ILNAS-EN ISO 8871-2:2004 Edition 09/2004
Elastomeric parts for parenterals and for devices for pharmaceutical use - Part 2: Identification and characterization (ISO 8871-2:2003)
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Abstract

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.

Status

Standard - Superseded

Origin

Technical Committee :
CEN/TC 205 : Non-active medical devices

Implementation

start of the vote on the project      date of ratification (dor)    15/07/2004
end of the vote on the project      date of anouncement (doa)    31/12/2004
start of the vote on the final project    27/11/2003   date of publication (dop)    31/03/2005
end of the vote on the final project    27/05/2004   date of withdrawal (dow)    31/03/2005


Publication Official Journal
of the Grand-Duchy of Luxembourg
04/02/2005
Reference

Relations

Evolutions
ILNAS-EN ISO 8871-2:2020
ILNAS-EN ISO 8871-2:2004/A1:2014

Relations to older standards
ILNAS-EN ISO 8871:1997/A1:1999
ILNAS-EN ISO 8871:1997

International Classification for Standards (ICS codes) :

11.040.20 : Transfusion, infusion and injection equipment

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