This part of ISO 18113 defines concepts, establishes general principles and specifies essential requirements for information supplied by the manufacturer of IVD medical devices. This part of ISO 18113 does not address language requirements, since that is the domain of national laws and regulations. This part of ISO 18113 does not apply to a)IVD devices for performance evaluation (e.g., for investigational use only), b)instrument marking, c)material safety data sheets.
DIN EN ISO 18113-1-2013由德國標準化學會 DE-DIN 發布于 2013-01,并于 2013-01-01 實施。
DIN EN ISO 18113-1-2013 在中國標準分類中歸屬于: C38 普通診察器械。
* 在 DIN EN ISO 18113-1-2013 發布之后有更新,請注意新發布標準的變化。
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