GB/T 16886.2-2026
医疗器械生物学评价 第2部分:动物福利要求
Biological evaluation of medical devices—Part 2: Animal welfare requirements
- 实施日期
- 2027-02-01
- 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 39 条
GB/T 16886.2-2026
Biological evaluation of medical devices—Part 2: Animal welfare requirements
GB/T 16886.17-2025
Biological evaluation of medical devices—Part 17:Toxicological risk assessment of medical device constituents
GB/T 16886.10-2024
Biological evaluation of medical devices—Part 10:Tests for skin sensitization
GB/T 16886.12-2023
Biological evaluation of medical devices—Part 12: Sample preparation and reference materials
GB/T 16886.23-2023
Biological evaluation of medical devices—Part 23: Tests for irritation
GB/T 16886.19-2022
Biological evaluation of medical devices—Part 19: Physico-chemical, morphological and topographical characterization of materials
GB/T 16886.18-2022
Biological evaluation of medical devices—Part 18: Chemical characterization of medical device materials within a risk management process
GB/T 16886.15-2022
Biological evaluation of medical devices—Part 15: Identification and quantification of degradation products from metals and alloys
GB/T 16886.9-2022
Biological evaluation of medical devices—Part 9:Framework for identification and quantification of potential degradation products
GB/T 16886.1-2022
Biological evaluation of medical devices—Part 1: Evaluation and testing within a risk management process
GB/T 16886.6-2022
Biological evaluation of medical devices—Part 6:Tests for local effects after implantation
GB/T 16886.4-2022
Biological evaluation of medical devices—Part 4: Selection of tests for interactions with blood
GB/T 16886.16-2021
Biological evaluation of medical devices—Part 16: Toxicokinetic study design for degradation products and leachables
GB/T 16886.11-2021
Biological evaluation of medical devices—Part 11: Tests for systemic toxicity
GB/T 16886.3-2019
Biological evaluation of medical devices—Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity
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