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SRPS EN ISO 8871-2:2010

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

Nov 29, 2010
95.99   Withdrawal of Standard   Dec 31, 2020

General information

95.99     Dec 31, 2020

ISS

Z076

European Norm

11.040.20  

English  

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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

NOW

WITHDRAWN
SRPS EN ISO 8871-2:2010
95.99 Withdrawal of Standard
Dec 31, 2020

REVISED BY

PUBLISHED
SRPS EN ISO 8871-2 :2020

Related project

Adopted from EN ISO 8871-2:2004

Adopted from ISO 8871-2:2003 IDENTICAL