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 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 this part of ISO9187 are intended for single use only.
DIN EN ISO 9187-1-2008由德国标准化学会 DE-DIN 发布于 2008-06。
DIN EN ISO 9187-1-2008 在中国标准分类中归属于: C31 一般与显微外科器械,在国际标准分类中归属于: 11.040.20 输血、输液和注射设备。
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