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DIN ISO 13926-2:2012-09

Superseded

Superseded

A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.

View Superseded by

PEN SYSTEMS - PART 2: PLUNGER STOPPERS FOR PEN-INJECTORS FOR MEDICAL USE (ISO 13926-2:2011)

Available format(s)

Hardcopy , PDF

Superseded date

31-08-2018

Superseded by

DIN ISO 13926-2:2018-07

Language(s)

English, German

Published date

01-01-2012

€66.07
Excluding VAT

National foreword
National Annex NA (informative) - Bibliography
Introduction
1 Scope
2 Normative references
3 Classification
4 Shape and dime
5 Designation
6 Material
7 Requirements
8 Labelling
Annex A (normative) - Leakage test
Bibliography

Describes the shape, dimensions, material, performance requirements and labelling of plunger stoppers for pen-injectors for medical use.

DocumentType
Standard
Pages
12
PublisherName
German Institute for Standardisation (Deutsches Institut für Normung)
Status
Superseded
SupersededBy

Standards Relationship
ISO 13926-2:2011 Identical

ISO 8871-1:2003 Elastomeric parts for parenterals and for devices for pharmaceutical use — Part 1: Extractables in aqueous autoclavates
ISO 7619-1:2010 Rubber, vulcanized or thermoplastic Determination of indentation hardness Part 1: Durometer method (Shore hardness)
ISO 13926-3:2012 Pen systems Part 3: Seals for pen-injectors for medical use
ISO 13926-1:2004 Pen systems Part 1: Glass cylinders for pen-injectors for medical use
DIN ISO 13926-1:2005-10 PEN SYSTEMS - PART 1: GLASS CYLINDERS FOR PEN-INJECTORS FOR MEDICAL USE
ISO 2230:2002 Rubber products — Guidelines for storage
DIN EN ISO 8871-1:2004-11 ELASTOMERIC PARTS FOR PARENTERALS AND FOR DEVICES FOR PHARMACEUTICAL USE - PART 1: EXTRACTABLE IN AQUEOUS AUTOCLAVATES
ISO 11608-3:2012 Needle-based injection systems for medical use Requirements and test methods Part 3: Finished containers
ISO 15378:2017 Primary packaging materials for medicinal products — Particular requirements for the application of ISO 9001:2015, with reference to good manufacturing practice (GMP)
DIN EN ISO 8871-4:2006-09 Elastomeric parts for parenterals and for devices for pharmaceutical use - Part 4: Biological requirements and test methods (ISO 8871-4:2006)
ISO 48:2010 Rubber, vulcanized or thermoplastic Determination of hardness (hardness between 10 IRHD and 100 IRHD)
ISO 8871-4:2006 Elastomeric parts for parenterals and for devices for pharmaceutical use Part 4: Biological requirements and test methods

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