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SSH EN ISO 8871-2:2004

Pjesët prej elastomeri për parenteralet dhe për pajisjet për përdorime farmaceutike - Pjesa 2: Identifikimi dhe tipizimi

Elastomeric parts for parenterals and for devices for pharmaceutical use - Part 2: Identification and characterization (ISO 8871-2:2003)
1 shk 2007
95.99 Withdrawal of Standard   29 qer 2021

General information

95.99     29 qer 2021

DPS

DPS/KT 205

European Norm

11.040.20  

anglisht  

Buying

Shfuqizuar

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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WITHDRAWN
SSH EN ISO 8871-2:2004
95.99 Withdrawal of Standard
29 qer 2021

REVISED BY

PUBLISHED
SSH EN ISO 8871-2:2020

Related project

Adopted from EN ISO 8871-2:2004