This part of ISO 9187 specifies materials, dimensions, capacities, performance and packaging requirements for three forms of glass ampoule (forms B, C and D) for injectable pharmaceutical products.
It applies to ampoules with or without a colour break-ring.
If ampoules with a colour break-ring are requested by the user, this should be agreed between manufacturer and user, including a decision on break-ring colour.
Ampoules complying with this part of ISO 9187 are intended for single use only.
ISO 9187-1:2000 history
2010ISO 9187-1:2010 Injection equipment for medical use - Part 1: Ampoules for injectables
2006ISO 9187-1:2006 Injection equipment for medical use - Part 1: Ampoules for injectables
2000ISO 9187-1:2000 Injection equipment for medical use - Part 1: Ampoules for injectables
1991ISO 9187-1:1991 Injection equipment for medical use; part 1: ampoules for injectables