prEN ISO 8871-3 rev

Elastomeric parts for parenterals and for devices for pharmaceutical use — Part 3: Determination of released-particle count prEN ISO 8871-3 rev

General information

10.99   New project approved   May 29, 2025

CEN

CEN/TC 205 Non-active medical devices

European Norm

Scope

Elastomeric closures may be superficially contaminated with visible and subvisible particles, and fragments can also be produced when the closure is pierced by a needle.
Such particles may be transferred to pharmaceutical preparations in contact with the elastomeric parts and affect the quality of such preparations.
ISO 8871-3:2003 specifies methods for the determination of the number of visible and subvisible particles, respectively, detached from elastomeric parts by rinsing.
It does not specify particle contamination limits. These will have to be agreed upon between manufacturer and user.

Life cycle

PREVIOUSLY

PUBLISHED
EN ISO 8871-3:2004/A1:2019

PUBLISHED
EN ISO 8871-3:2004

NOW

IN_DEVELOPMENT
prEN ISO 8871-3 rev
10.99 New project approved
May 29, 2025




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