DS/EN ISO 9187-1-2011

Injection equipment for medical use - Part 1: Ampoules for injectables

DS/EN ISO 9187-1-2011 发布历史

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 ISO 9187 are intended for single use only.

DS/EN ISO 9187-1-2011由丹麦标准化协会 DK-DS 发布于 2011-04-14，并于 2011-04-14 实施。

DS/EN ISO 9187-1-2011在国际标准分类中归属于: 11.040.20 输血、输液和注射设备。

DS/EN ISO 9187-1-2011的历代版本如下：

• 2011年04月14日 DS/EN ISO 9187-1-2011

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标准号

DS/EN ISO 9187-1-2011

发布日期

2011年04月14日

实施日期

2011年04月14日

废止日期

无

国际标准分类号

11.040.20

发布单位

DK-DS

被代替标准

DS/EN ISO 9187-1-2008

适用范围

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 ISO 9187 are intended for single use only.

DS/EN ISO 9187-1-2011系列标准