无源医疗器械的生物学ISO10993测试当中，包含共17条测试标准
生物相容性分类分别为细胞毒性，刺激及皮肤致敏，材料介入导致热源，急性全身毒性，亚急性毒性，亚慢性毒性，慢性毒性，植入效果，血液相容性，基因毒性，致癌性，生殖与发育毒性等......
我们应先判定器械的种类，接触部位，接触时间，判定如何选择测试标准
测试标准如下：
ISO 10993-2:2006, Biological evaluation of medical devices —Part 2: Animal welfare requirements
ISO 10993-3, Biological evaluation of medical devices — Part 3:Tests for genotoxicity, carcinogenicity and reproductivetoxicity
ISO 10993-4, Biological evaluation of medical devices — Part 4:Selection of tests for interactions with blood
ISO 10993-5, Biological evaluation of medical devices — Part 5:Tests for in vitro cytotoxicity
ISO 10993-6, Biological evaluation of medical devices — Part 6:Tests for local effects after implantation
ISO 10993-7, Biological evaluation of medical devices — Part 7:Ethylene oxide sterilization residuals
ISO 10993-9, Biological evaluation of medical devices — Part 9:Framework for identification and of potentialdegradation products
ISO 10993-10, Biological evaluation of medical devices — Part10: Tests for irritation and skin sensitization
ISO 10993-11:2017, Biological evaluation of medical devices —Part 11: Tests for systemic toxicity
ISO 10993-12, Biological evaluation of medical devices — Part12: Sample preparation and reference materials
ISO 10993-13, Biological evaluation of medical devices — Part13: Identification and of degradation products frompolymeric medical devices
ISO 10993-14, Biological evaluation of medical devices — Part14: Identification and of degradation products fromceramics
ISO 10993-15, Biological evaluation of medical devices — Part15: Identification and of degradation products frommetals and alloys
ISO 10993-16, Biological evaluation of medical devices — Part16: Toxicokinetic study design for degradation products andleachables
ISO 10993-17, Biological evaluation of medical devices — Part17: Establishment of allowable limits for leachable substances
ISO 10993-18, Biological evaluation of medical devices — Part18: Chemical characterization of materials
ISO/TS 10993-20, Biological evaluation of medical devices — Part20: Principles and methods for immunotoxicology testing of medicaldevices
判定方式如下：
根据ISO 10993-1:2018(E)当中的Figure 1 — Summary of the systematicapproach to a biological evaluation of medical devices as part of arisk management process
根据器械特点，判定流程走向
再结合Table A.1 — Endpoints to be addressed in a biological riskassessment
生物学进行综合评估，需要结合制造风险（ISO14971:2019）判定生产工艺流程，是否引入新的生物风险源
总结
生物学报告需要总结出两项内容
1，设备做的生物学检测，是否满足需求
2，制造风险是否有新的生物风险，并且得到控