This part of ISO 8871 specifies biological requirements for elastomeric parts for parenterals and for devices for pharmaceutical use. It also specifies the test methods, i.e. it offers the extraction procedures for elastomeric parts, and it makes reference to relevant biological test instructions in Pharmacopoeias and standards.
DIN EN ISO 8871-4-2006由德国标准化学会 DE-DIN 发布于 2006-09。
DIN EN ISO 8871-4-2006 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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