11.100.20 标准查询与下载



共找到 324 条与 相关的标准,共 22

Medical products containing viable human cells. Application of risk management and requirements for processing practices

ICS
11.100.20
CCS
C30
发布
2016
实施
2017-01-01

Medical devices. Biological evaluation of medical devices. Part 16. Toxicokinetic study design for degradation products and leachables

ICS
11.100.20
CCS
发布
2016
实施
2017-10-01

Medical devices. Biological evaluation of medical devices. Part 13. Identification and quantification of degradation products from polymeric medical devices

ICS
11.100.20
CCS
发布
2016
实施
2017-10-01

Medical devices. Biological evaluation of medical devices. Part 7. Ethylene oxide sterilization residuals

ICS
11.100.20
CCS
发布
2016
实施
2017-10-01

Medical devices utilizing animal tissues and their derivatives. Controls on sourcing, collection and handling

ICS
11.100.20
CCS
C37
发布
2015-12-31
实施
2015-12-31

  Scope is not provided for this standard

Biological evaluation of medical devices -- Part 2: Animal welfare requirements

ICS
11.100.20
CCS
发布
2015-12-21
实施

  Scope is not provided for this standard

Biological evaluation of medical devices -- Part 11: Tests for systemic toxicity

ICS
11.100.20
CCS
发布
2015-12-21
实施

  Scope is not provided for this standard

Biological evaluation of medical devices -- Part 5: Tests for in vitro cytotoxicity

ICS
11.100.20
CCS
发布
2015-12-21
实施

  Scope is not provided for this standard

Biological evaluation of medical devices -- Part 6: Tests for local effects after implantation

ICS
11.100.20
CCS
发布
2015-12-21
实施

  Scope is not provided for this standard

Biological evaluation of medical devices -- Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity

ICS
11.100.20
CCS
发布
2015-12-21
实施

  Scope is not provided for this standard

Clinical investigation of medical devices for human subjects -- Good clinical practice

ICS
11.100.20
CCS
发布
2015-12-21
实施

  Scope is not provided for this standard

Biological evaluation of medical devices -- Part 16: Toxicokinetic study design for degradation products and leachables

ICS
11.100.20
CCS
发布
2015-12-21
实施

  Scope is not provided for this standard

Biological evaluation of medical devices -- Part 7: Ethylene oxide sterilization residuals

ICS
11.100.20
CCS
发布
2015-12-21
实施

为帮助确定无活力动物组织来源的医疗器械的加工过程是否有助于减少传播性海绵状脑病(TSEs)的医源性传播的风险,本部分为设计和开展确认分析提供建议。加工动物组织所使用的TSE去除方法也宜减少通过人源性无活力组织传播TSE感染的风险;本部分不涉及这一方面。一些关于人体组织和TSEs的当前信息可通过类推适用于其他动物组织。本部分不预期为ISO 22442-1:2007的附录C中所列出的已识别出的具有TSE因子污染的“可忽略风险”的特定材料提供方法的确认要求。本部分预期用于解释ISO 22442系列中最终国际标准草案以及ISO 14160标准。本部分是建立在对ISO 22442-3中与TSE因子相关的特定讨论的基础之上并努力总结TSE因子去除领域内当前最新技术水平。随着对TSE因子的灭活和去除的深入理解,可行时将会对本文件进行修订。

Medical devices utilizing animal tissues and their derivatives.Part 4:Principles for elimination and/or inactivation of transmissible spongiform encephalopathy agents and validation assays for those processes

ICS
11.100.20
CCS
C30
发布
2015-03-02
实施
2016-01-01

Biological evaluation of medical devices - Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity (ISO 10993-3:2014); German version EN ISO 10993-3:2014

ICS
11.100.20
CCS
C30
发布
2015-02
实施

Medical devices. Biological evaluation of medical devices. Part 9. Framework for identification and quantification of potential degradation products

ICS
11.100.20
CCS
发布
2015
实施
2016-06-01

Medical devices. Biological evaluation of medical devices. Part 12. Sample preparation and reference materials

ICS
11.100.20
CCS
发布
2015
实施
2016-06-01

Biological evaluation of medical devices — Part 12: Sample preparation and reference materials

ICS
11.100.20
CCS
发布
2014-12-01
实施
2014-12-01

Biological evaluation of medical devices. Tests for genotoxicity, carcinogenicity and reproductive toxicity

ICS
11.100.20
CCS
C30
发布
2014-10-31
实施
2014-10-31

Biological evaluation of medical devices - Part 10: Tests for irritation and skin sensitization (ISO 10993-10:2010); German version EN ISO 10993-10:2013

ICS
11.100.20
CCS
C30
发布
2014-10-01
实施



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