prEN ISO 8871-2 rev

Elastomeric parts for parenterals and for devices for pharmaceutical use — Part 2: Identification and characterization prEN ISO 8871-2 rev

General information

10.99   New project approved   Oct 14, 2025

CEN

CEN/TC 205 Non-active medical devices

European Norm

Scope

This document specifies identification and characterization procedures applicable to elastomeric parts including coated stoppers used for drug containers and medical devices.
The physical and chemical test procedures specified in this document permit the determination of the typical characteristics of elastomeric parts including coatings and surface treatments and can serve as a basis for agreements between manufacturer and user regarding the product consistency in subsequent supplies. Depending upon the type of elastomer and its application, an appropriate set of tests is selected.

Life cycle

PREVIOUSLY

PUBLISHED
EN ISO 8871-2:2020

NOW

IN_DEVELOPMENT
prEN ISO 8871-2 rev
10.99 New project approved
Oct 14, 2025




Access Genorma App Everywhere

Get fast and easy access to top European and International standards (EN, ISO, IEC) via your mobile phone, tablet or the web.