GB/T 16886.11-1997
Replaced
YY/T 1670.2-2025
Pending
Industry standards-Medicine
YY/T 1670.2-2025 Neurotoxicity evaluation of medical devices—Part 2:Tests for neuro-cytotoxicity
YY/T 1670.2-2025 Neurotoxicity evaluation of medical devices—Part 2:Tests for neuro-cytotoxicity
Basic Information
Standard Code:
YY/T 1670.2-2025
Standard Type:
Industry standards
Standard Status:
Pending
is_force_gb:
no
CCS Name:
Medical devices
ICS Name:
Integrated medical equipment
Publish Date:
2025-10-30
Implement Date:
2026-11-01
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:
16 pages
Scope
本文件描述了对医疗器械/生物材料进行神经细胞毒性评价的试验方法。
本文件适用于直接或间接与神经系统接触的医疗器械/生物材料的神经细胞毒性评价。
Development Information
Drafting Units:
中国食品药品检定研究院、山东省医疗器械和药品包装检验研究院、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)、四川大学(四川医疗器械生物材料和制品检验中心有限公司)
Drafting Persons:
魏利娜、刘佳、王蕊、蔡永福、盖潇潇、贾文思、徐爽、贾莉芳、陈丽媛、方海燕、陈亮
Referenced Standards
GB/T 16886.5-2003 Biological evaluation of medical devices—Part 5:Test for in vitro cytotoxicity
GB/T 16886.5-2017 Biological evaluation of medical devices—Part 5:Tests for in vitro cytotoxicity
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
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