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INFORMATION SUPPLIED BY THE MANUFACTURER OF MEDICAL DEVICES
出版:Comite Europeen de Normalisation

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基本信息
標(biāo)準(zhǔn)編號(hào): EN 1041 : 2008 + A1 2013
標(biāo)準(zhǔn)類別:Standard
出版單位:Comite Europeen de Normalisation
標(biāo)準(zhǔn)頁(yè)數(shù):0
標(biāo)準(zhǔn)簡(jiǎn)介
Describes requirements for information to be supplied by a manufacturer for medical devices regulated by Council Directive 90/385/EEC relating to active implantable medical devices and Council Directive 93/42/EEC concerning medical devices.