GB/T 16886.9-2017
医疗器械生物学评价 第9部分:潜在降解产物的定性和定量框架
Biological evaluation of medical devices—Part 9: Framework for identification and quantification of potential degradation products
- 实施日期
- 2018-07-01
- ICS 分类
- 11.100.20
组合使用关键词、标准类型、状态与 ICS 分类,快速定位所需国家标准。
找到 167 条
GB/T 16886.9-2017
Biological evaluation of medical devices—Part 9: Framework for identification and quantification of potential degradation products
GB/T 16886.5-2017
Biological evaluation of medical devices—Part 5: Tests for in vitro cytotoxicity
GB/T 16886.13-2017
Biological evaluation of medical devices—Part 13: Identification and quantification of degradation products from polymeric medical devices
GB/T 16886.12-2017
Biological evaluation of medical devices—Part 12:Sample preparation and reference materials
GB/T 16886.10-2017
Biological evaluation of medical devices—Part 10: Tests for irritation and skin sensitization
GB/T 33752-2017
Aldehyde slide for microarrays
GB/T 16886.7-2015
Biological evaluation of medical devices—Part 7: Ethylene oxide sterilization residuals
GB/T 16886.20-2015
Biological evaluation of medical devices—Part 20: Principles and methods for immunotoxicology testing of medical devices
GB/T 30224-2013
Clinical use of tests for toxoplasma gondii
GB/Z 30154-2013
Medical laboratories―Guidance on laboratory implementation of GB/T 22576-2008
GB/T 16886.16-2013
Biological evaluation of medical devices―Part 16: Toxicokinetic study design for degradation products and leachables
GB/T 29790-2013
Point-of-care testing(POCT) - Requirements for quality and competence
GB/T 29791.5-2013
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 5: In vitro diagnostic instruments for selftesting
GB/T 29791.4-2013
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 4: In vitro diagnostic reagents for selftesting
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
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
GB/T 29791.1-2013
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions and general requirements
GB/T 29764-2013
Chemicals-fish (Oryzias latipes, d-rR Medaka) early life stage toxicity test
GB/T 29763-2013
Chemicals - Rare Minnow (Gobiocypris rarus) acute toxicity test
GB/T 28648-2012
Chemicals - Acute inhalation toxicity testing - Acute toxic class method