GB/T 16886.11-1997
Replaced
YY/T 0870.8-2024
Active
Industry standards-Medicine
YY/T 0870.8-2024 Test for genotoxicity of medical devices—Part 8:Unscheduled DNA synthesis test with mammalian liver cells in vivo
YY/T 0870.8-2024 Test for genotoxicity of medical devices—Part 8:Unscheduled DNA synthesis test with mammalian liver cells in vivo
Basic Information
Standard Code:
YY/T 0870.8-2024
Standard Type:
Industry standards
Standard Status:
Active
is_force_gb:
no
CCS Name:
Medical devices
ICS Name:
Integrated medical equipment
Publish Date:
2024-07-08
Implement Date:
2025-07-20
Publisher:
国家药品监督管理局
Technical Committee:
全国医疗器械生物学评价标准化技术委员会(SAC/TC 248)
Pages:
12 pages
Scope
本文件描述了医疗器械体内哺乳动物肝细胞程序外DNA合成试验方法。
本文件适用于通过测定医疗器械引起的哺乳动物肝细胞程序外DNA损伤,评价医疗器械是否具有潜在遗传毒性作用。
注: 纳米材料的体内哺乳动物肝细胞程序外DNA合成试验可能需要对本文件中的方法进行特定的修订,但本文件未给予描述。
Development Information
Drafting Units:
山东省医疗器械和药品包装检验研究院、上海交通大学医学院附属第九人民医院、北京市医疗器械检验研究院(北京市医用生物防护装备检验研究中心)
Drafting Persons:
王鸾鸾、刘昕、宋伟、孙皎、张奥、褚祥宇、车国喜
Referenced Standards
GB 14925-2001 Laboratory animal—Requirements of environment and housing facilities
GB 14925-2010 Laboratory animal—Requirements of environment and housing facilities
GB 14925-2023 Laboratory animal—Environment and housing facilities
GB/T 16886.2-2000 Biological evaluation of medical devices—Part 2:Animal welfare requirements
GB/T 16886.2-2011 Biological evaluation of medical devices—Part 2:Animal welfare requirements
GB/T 16886.3-1997 Biological evaluation of medical devices—Part 3:Tests for genotoxicity, carcinogenicity and reproductive toxicity
GB/T 16886.3-2008 Biological evaluation of medical devices—Part 3:Tests for genotoxicity,carcinogenicity and reproductive toxicity
GB/T 16886.3-2019 Biological evaluation of medical devices—Part 3:Tests for genotoxicity, carcinogenicity and reproductive toxicity
GB/T 16886.12-2000 Biological evaluation of medical devices—Part 12:Sample preparation and reference materials
GB/T 16886.12-2005 Biological evaluation of medical devices—Part 12:Sample preparation and reference materials
GB/T 16886.12-2017 Biological evaluation of medical devices—Part 12:Sample preparation and reference materials
GB/T 16886.12-2023 Biological evaluation of medical devices—Part 12:Sample preparation and reference materials
GB/T 16886.2-2026 Biological evaluation of medical devices—Part 2:Animal welfare requirements
Related Standards
GB/T 16886.3-1997
Replaced
GB/T 16886.3-1997 Biological evaluation of medical devices—Part 3:Tests for genotoxicity, carcinogenicity and reproductive toxicity
GB/T 16886.6-1997
Replaced
GB/T 16886.6-1997 Biological evaluation of medical devices—Part 6:Tests for local effects after implantation
GB/T 16886.1-2001
Replaced
GB/T 16886.1-2001 Biological evaluation of medical devices—Part 1:Evaluation and testing
GB/T 16886.13-2001
Replaced
GB/T 16886.13-2001 Biological evaluation of medical devices—Part 13:Identification and quantification of degradation products from polymeric medical devices
GB/T 16886.7-2001
Replaced