標(biāo)準(zhǔn)號：DIN EN ISO 18113-3-2013
中文標(biāo)準(zhǔn)名稱：體外診斷醫(yī)療器械.制造商提供的信息(標(biāo)簽).第3部分:專業(yè)用體外診斷儀器(ISO 18113-3-2009).德文版本EN ISO 18113-3-2011
英文標(biāo)準(zhǔn)名稱：In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 3: In vitro diagnostic instruments for professional use (ISO 18113-3:2009); German version EN ISO 18113-3:2011
標(biāo)準(zhǔn)類型：C38
發(fā)布日期：1999/12/31 12:00:00
實(shí)施日期：2013/1/1 12:00:00
中國標(biāo)準(zhǔn)分類號：C38
國際標(biāo)準(zhǔn)分類號：11.100.10
引用標(biāo)準(zhǔn)：ISO 14971;ISO 15223-1;ISO 18113-1;IEC 61010-1;IEC 61010-2-101;IEC 61326-2-6;IEC 62366;EN 980
適用范圍：This part of ISO 18113 specifies requirements for information supplied by the manufacturer of IVD instruments for professional use.This part of ISO 18113 also applies to apparatus and equipment intended to be used with IVD instruments for professional use.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 self-testing.