In vitro diagnostic medical devices—Information supplied by the manufacturer(labelling)—Part 1:Terms,definitions and general requirements
IDT ISO 18113-1:2009
全国医用临床检验实验室和体外诊断系统标准化技术委员会(SAC/TC 136)
GB/T 29791的本部分对体外诊断医疗器械制造商所提供的信息定义概念、建立一般原则并规定基本要求。
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