DZ/T 0101.12-1994
Active
YY/T 1240-2023
Active
Industry standards-Medicine
YY/T 1240-2023 D-dimer testing kit(Immune turbidity method)
YY/T 1240-2023 D-dimer testing kit(Immune turbidity method)
Basic Information
Standard Code:
YY/T 1240-2023
Standard Type:
Industry standards
Standard Status:
Active
is_force_gb:
no
CCS Name:
Medical laboratory equipment
ICS Name:
-
Publish Date:
2023-01-13
Implement Date:
2023-07-15
Publisher:
国家药品监督管理局
Technical Committee:
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)
Pages:
16 pages
Scope
本文件规定了D-二聚体测定试剂盒（免疫比浊法）的要求、试验方法、标志、标签和使用说明书、包装、运输和贮存。
本文件适用于免疫比浊法测定D-二聚体的试剂盒产品(以下简称D-二聚体试剂）。
Development Information
Drafting Units:
中国人民解放军总医院第一医学中心、北京市医疗器械检验研究院、北京市医疗器械审评检查中心、吉林省药品审评中心、山东艾科达生物科技有限公司、希森美康医用电子(上海)有限公司、北京思塔高诊断产品贸易有限责任公司、北京赛科希德科技股份有限公司、深圳迈瑞生物医疗电子股份有限公司
Drafting Persons:
李绵洋、续勇、孙嵘、刘柳、邸平、李健、李覃、郭鑫、丁重辉、赵玉梅
Replace the following standards
Referenced Standards
GB/T 29791.2-2013 In vitro diagnostic medical devices—Information supplied by the manufacturer (labelling)—Part 2:In vitro diagnostic reagents for professional use
YY/T 0466.1-2009 Medical devices—Symbols to be used with medical device labels, labelling and information to be supplied—Part 1:General requirements
YY/T 0466.1-2016 Medical devices—Symbols to be used with medical device labels,labelling and information to be supplied—Part 1:General requirements
YY/T 0466.1-2023 Medical devices—Symbols to be used with information to be supplied by the manufacturer—Part 1:General requirements
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