ISO 9187-1:2010
Current
The latest, up-to-date edition.
Injection equipment for medical use — Part 1: Ampoules for injectables
Hardcopy , PDF
French, English
30-09-2010
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 |
ISO/TC 76
|
| DevelopmentNote |
Supersedes ISO/DIS 9187-1. (10/2010)
|
| DocumentType |
Standard
|
| Pages |
9
|
| PublisherName |
International Organization for Standardization
|
| Status |
Current
|
| Supersedes |
| Standards | Relationship |
| NF EN ISO 9187-1 : 2010 | Identical |
| NEN EN ISO 9187-1 : 2010 | Identical |
| NS EN ISO 9187-1 : 2010 | Identical |
| I.S. EN ISO 9187-1:2010 | Identical |
| PN EN ISO 9187-1 : 2011 | Identical |
| SAC GB/T 2637 : 2016 | Identical |
| SS-EN ISO 9187-1:2010 | Identical |
| BS EN ISO 9187-1:2010 | Identical |
| EN ISO 9187-1:2010 | Identical |
| DIN EN ISO 9187-1:2011-01 | Identical |
| IS 15537 : 2021 | Identical |
| DIN ISO 9187-1:2000-12 | Identical |
| NF ISO 9187-1 : 1992 | Identical |
| NEN ISO 9187-1 : 2006 | Identical |
| UNE-EN ISO 9187-1:2011 | Identical |
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