DIN EN ISO 18113-5-2013
体外诊断医疗器械.制造商提供的信息(标签).第5部分:自测用体外诊断仪器(ISO 18113-5-2009).德文版本EN ISO 18113-5-2011

In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 5: In vitro diagnostic instruments for self-testing (ISO 18113-5:2009); German version EN ISO 18113-5:2011


 

 

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标准号
DIN EN ISO 18113-5-2013
发布日期
2013年01月
实施日期
废止日期
中国标准分类号
C38
国际标准分类号
11.100.10
发布单位
DE-DIN
引用标准
ISO 14971 ISO 15223-1 ISO 18113-1 IEC 61010-1 IEC 61010-2-101 IEC 61326-2-6 IEC 62366 EN 980
被代替标准
DIN EN ISO 18113-5-2010
适用范围
This part of ISO 18113 specifies requirements for infornation supplied by the manufacturer of IVD instruments for self-testing. This part of ISO 18113 also applies to apparatus and equipment intended to be used with IVD instruments for self-testing. This part of ISO 18113 can also be applied to accessories. This part of ISO 18113 does not apply to a)instructions for instrument servicing or repair, b)IVD reagents, including calibrators and control materials for use in control of the reagent, c)IVD instruments for professional use.

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