GB 8662-1988
Replaced
YY/T 1723-2020
Active
Industry standards-Medicine
YY/T 1723-2020 High-throughput gene sequencer
YY/T 1723-2020 High-throughput gene sequencer
Basic Information
Standard Code:
YY/T 1723-2020
Standard Type:
Industry standards
Standard Status:
Active
is_force_gb:
no
CCS Name:
Medical devices
ICS Name:
Surgical instruments and materials
Publish Date:
2020-06-30
Implement Date:
2021-12-01
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
本标准规定了高通量基因测序仪的要求、试验方法、标签和使用说明书、包装、运输和贮存。
本标准适用于半导体测序法、可逆末端终止测序法、联合探针锚定聚合测序法、联合探针锚定连接测序法、焦磷酸测序等技术为主要技术原理的并行测序高通量基因测序仪。
本标准不适用于桑格（Sanger）测序为主要技术原理的基因测序仪。
本标准不适用于全内反射显微镜、生物纳米孔、固态纳米孔技术等为主要技术原理的单分子测序的高通量基因测序仪。
Development Information
Drafting Units:
中国食品药品检定研究院、深圳华大智造科技有限公司、广州市达瑞生物技术股份有限公司、北京市医疗器械检验所、东莞博奥木华基因科技有限公司、天津诺禾致源生物信息科技有限公司、杭州贝瑞和康基因诊断技术有限公司、安诺优达基因科技(北京)有限公司、宜曼达贸易(上海)有限公司
Drafting Persons:
黄杰、蒋慧、吴英松、李达、黄铨飞、邹浩、张建光、刘三阳、张素芳、曲守方、于婷
Referenced Standards
GB/T 191-2000 Packaging—Pictorial marking for handling of goods
GB/T 191-2008 Packaging—Pictorial marking for handling of goods
GB 4793.1-1995 Safety requirements for electrical equipment for measurement, control, and laboratory use Part 1:General requirements
GB 4793.1-2007 Safety requirements for electrical equipment for measurement, control, and laboratory use—Part 1:General requirements
GB 4793.9-2013 Safety requirements for electrical equipment for measurement,control and laboratory use—Part 9:Particular requirements for automatic and semi-automatic laboratory equipment for analysis and other purposes
GB/T 14710-1993 The environmental requirements and test methods for medical electrical equipment
GB/T 14710-2009 Environmental requirement and test methods for medical electrical equipment
GB/T 18268.1-2010 Electrical equipment for measurement,control and laboratory use—EMC requirements—Part 1:General requirements
GB/T 18268.26-2010 Electrical equipment for measurement,control and laboratory use—EMC requirements—Part 26:Particular requirements—In vitro diagnostic (IVD) medical equipment
GB/T 29791.3-2013 In vitro diagnostic medical devices—Information supplied by the manufacturer(labelling)—Part 3:In vitro diagnostic instruments for professional use
YY 0648-2008 Safety requirements for electrical equipment for measurement,control and laboratory use—Part 2-101:Particular requirements for in vitro diagnostic (IVD) medical equipment
GB/T 18268.1-2025 Electrical equipment for measurement,control and laboratory use—EMC requirements—Part 1:General requirements
GB/T 191-2025 Graphical symbols marking for handling and storage of packages
YY/T 0648-2025 Safety requirements for electrical equipment for measurement,control,and laboratory use—Part 2-101:Particular requirements for in vitro diagnostic (IVD)medical equipment
Related Standards
GB 2766-1995
Replaced
GB 2766-1995 Haemostatic forceps with box joint—General specifications
GB/T 10160-1995
Abolished
GB/T 10160-1995 Test methods of locking force and opening force for medical use forceps
GB 9706.4-1999
Replaced
GB 9706.4-1999 Medical electrical equipment—Part 2:Particular requirements for the safety of high frequency surgical equipment
YY 0464-2003
Replaced
YY 0464-2003 Single use hemoperfutor
YY 0054-2003
Replaced