EN ISO 9187-1:2010
Current
The latest, up-to-date edition.
Injection equipment for medical use - Part 1: Ampoules for injectables (ISO 9187-1:2010)
15-10-2010
Foreword
Introduction
1 Scope
2 Normative references
3 Dimensions and designation
4 Material
5 Requirements
6 Test for breaking force
7 Delivery
8 Packaging
9 Marking
Bibliography
ISO 9187-1:2010 specifies materials, dimensions, capacities, performance and packaging requirements for three forms of glass ampoule (forms B, C and D) for injectable pharmaceutical products.ISO 9187-1:2010 is applicable to ampoules with and without a colour break-ring; the provision of ampoules with a colour break-ring, and the choice of colour of the break-ring, is subject to agreement between the manufacturer and user.Ampoules complying with ISO 9187-1:2010 are intended for single use only.
| Committee |
CEN/BT
|
| DocumentType |
Standard
|
| PublisherName |
Comite Europeen de Normalisation
|
| Status |
Current
|
| Standards | Relationship |
| I.S. EN ISO 9187-1:2010 | Identical |
| NEN EN ISO 9187-1 : 2010 | Identical |
| ISO 9187-1:2010 | Identical |
| NF EN ISO 9187-1 : 2010 | Identical |
| DIN EN ISO 9187-1:2011-01 | Identical |
| NS EN ISO 9187-1 : 2010 | Identical |
| PN EN ISO 9187-1 : 2011 | Identical |
| SS-EN ISO 9187-1:2010 | Identical |
| BS EN ISO 9187-1:2010 | Identical |
| NBN EN ISO 9187-1 : 2010 | Identical |
| UNE-EN ISO 9187-1:2011 | Identical |