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ISO 8871-2:2003

Elastomeric parts for parenterals and for devices for pharmaceutical use -- Part 2: Identification and characterization

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Kehtetu alates 14.05.2020
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Standardi ajalugu

Staatus
Kuupäev
Tüüp
Nimetus
14.05.2020
Põhitekst
22.07.2005
Muudatus
19.09.2003
Põhitekst
Põhitekst
ISO 8871:1990
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.

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