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由德國標準化學會 DE-DIN 發布于 2006-09。
DIN EN ISO 8871-4-2006 在中國標準分類中歸屬于: C31 一般與顯微外科器械,在國際標準分類中歸屬于: 11.040.20 輸血、輸液和注射設備。
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